An Optimized O9-1/Hydrogel System for Studying Mechanical Signals in Neural Crest Cells

Tram  P. Le; Xiaolei Zhao; Shannon Erhardt; Jianhua Gu; Huie Wang; Tina O. Findley; Jun Wang

doi:10.3791/62693

JoVE Journal > Developmental Biology

发育生物学

An Optimized O9-1/Hydrogel System for Studying Mechanical Signals in Neural Crest Cells

Published: August 13, 2021

doi:

10.3791/62693

Tram P. Le*¹, Xiaolei Zhao*¹, Shannon Erhardt^1,2, Jianhua Gu³, Huie Wang³, Tina O. Findley¹, Jun Wang^1,2

¹Department of Pediatrics, McGovern Medical School,The University of Texas Health Science Center at Houston, ²The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences,The University of Texas Health Science Center at Houston, ³SEM AFM Core in the Houston Methodist Hospital Research Institute

Summary

Detailed step-by-step protocols are described here for studying mechanical signals in vitro using multipotent O9-1 neural crest cells and polyacrylamide hydrogels of varying stiffness.

Abstract

Neural crest cells (NCCs) are vertebrate embryonic multipotent cells that can migrate and differentiate into a wide array of cell types that give rise to various organs and tissues. Tissue stiffness produces mechanical force, a physical cue that plays a critical role in NCC differentiation; however, the mechanism remains unclear. The method described here provides detailed information for the optimized generation of polyacrylamide hydrogels of varying stiffness, the accurate measurement of such stiffness, and the evaluation of the impact of mechanical signals in O9-1 cells, a NCC line that mimics in vivo NCCs.

Hydrogel stiffness was measured using atomic force microscopy (AFM) and indicated different stiffness levels accordingly. O9-1 NCCs cultured on hydrogels of varying stiffness showed different cell morphology and gene expression of stress fibers, which indicated varying biological effects caused by mechanical signal changes. Moreover, this established that varying the hydrogel stiffness resulted in an efficient in vitro system to manipulate mechanical signaling by altering gel stiffness and analyzing the molecular and genetic regulation in NCCs. O9-1 NCCs can differentiate into a wide range of cell types under the influence of the corresponding differentiation media, and it is convenient to manipulate chemical signals in vitro. Therefore, this in vitro system is a powerful tool to study the role of mechanical signaling in NCCs and its interaction with chemical signals, which will help researchers better understand the molecular and genetic mechanisms of neural crest development and diseases.

Introduction

Neural crest cells (NCCs) are a group of stem cells during vertebrate embryogenesis with a remarkable ability to migrate and contribute to the development of various organs and tissues. NCCs can differentiate into different cell types, including sensory neurons, cartilage, bone, melanocytes, and smooth muscle cells, depending on the location of axial origin and the local environmental guidance of the NCC¹^,². With the ability to differentiate into a wide array of cell types, genetic abnormalities that cause dysregulation at any stage of neural crest (NC) development can lead to numerous congenital diseases². For instance, perturbations during the formation, migration, and development of NCCs lead to developmental disorders known collectively as neurocristopathies¹^,³. These diseases range from craniofacial defects due to failure in NCC formation, such as Treacher Collins syndrome, to the development of various cancers due to NCC metastatic migratory ability, as seen in melanoma³^,⁴^,⁵^,⁶. Over the last few decades, researchers have made remarkable discoveries about the roles and mechanisms of NCCs in development and diseases, with the majority of findings being focused on chemical signals⁷^,⁸. More recently, mechanical signals have been indicated to play a critical but poorly understood role in NCC development⁹^,¹⁰.

The environmental cues of NCCs play a critical role during their development, including the regulation of NCC differentiation into various cell types. Environmental cues, e.g., physical cues, influence pivotal behaviors and cellular responses, such as functional diversification. Mechanotransduction allows cells to sense and respond to those cues to maintain various biological processes². NCCs are surrounded by neighboring cells and different substrates, such as the extracellular matrix (ECM), which can give rise to mechanical stimuli to maintain homeostasis and adapt to the changes through fate determination, proliferation, and apoptosis¹¹. Mechanotransduction begins at the plasma membrane where the sensory component of mechanical extracellular stimuli occurs, resulting in the intracellular regulation of the cell¹². Integrins, focal adhesions, and junctions of the plasma membrane relay mechanical signals, such as shearing forces, stress, and the stiffness of surrounding substrates, into chemical signals to produce cellular responses¹². The relaying of chemical signals from the plasma membrane to the final cellular regulation is carried out via different signaling pathways to finalize vital processes for the organism, such as differentiation.

Several studies have suggested that mechanical signaling from substrate stiffness plays a role in cell differentiation¹³^,¹⁴. For instance, previous studies have shown that mesenchymal stem cells (MSCs) grown on soft substrates with a stiffness similar to that of brain tissue (in the range of 0.1-1.0 kPa) resulted in neuronal cell differentiation¹⁵^,¹⁶. However, more MSCs differentiate into myocyte-like cells when grown on 8-17 kPa substrates mimicking the stiffness of muscle, while osteoblast-like differentiation was observed when MSCs were cultured on stiff substrates (25-40 kPa)¹⁵^,¹⁶. The significance of mechanotransduction is highlighted by the irregularities and abnormalities in the mechanical signaling pathway that potentially lead to severe developmental defects and diseases, including cancer, cardiovascular diseases, and osteoporosis¹⁷^,¹⁸^,¹⁹. In cancers, normal breast tissue is soft, and the risk of breast cancer increases in stiff and dense breast tissue, an environment that is more akin to breast tumors¹⁵. With this knowledge, the effects of mechanical signaling on NCC development can be studied through simple manipulation of substrate stiffness through an in vitro system, providing further advantages and possibilities in understanding the fundamentals of NC-related disease progression and etiology.

To study the impact of mechanical signals in NCCs, we established an efficient in vitro system for NCCs based on the optimization of previously published methods and evaluation of the responses of NCCs to different mechanical signals²⁰^,²¹. A detailed protocol was provided for varying hydrogel stiffness preparation and evaluation of the impact of mechanical signaling in NCCs. To achieve this, O9-1 NCCs are utilized as the NC model to study the effects and changes in response to stiff versus soft hydrogels. O9-1 NCCs are a stable NC cell line isolated from mouse embryo (E) at day 8.5. O9-1 NCCs mimic NCCs in vivo because they can differentiate into various NC-derived cell types in defined differentiation media²². To study the mechanical signaling of NCCs, a matrix substrate was fabricated with tunable elasticity from varying concentrations of acrylamide and bis-acrylamide solutions to achieve the desired stiffness, correlating to the biological substrate stiffness²⁰^,²¹^,²³. To optimize the conditions of matrix substrate for NCCs, specifically O9-1 cells, modifications were made from the previously published protocol²⁰. One change made in this protocol was to incubate hydrogels in collagen I, diluted in 0.2% acetic acid instead of 50 mM HEPES, at 37 °C overnight. The low pH of acetic acid leads to a homogeneous distribution and higher collagen I incorporation, thus allowing for a more uniform attachment of the ECM protein²⁴. In addition, a combination of horse serum and fetal bovine serum (FBS) was used at the concentrations of 10% and 5% in phosphate buffer saline (PBS), respectively, before storing the hydrogels in the incubator. Horse serum was used as an additional supplement to FBS due to its ability to promote cell proliferation and differentiation at the concentration of 10%²⁵.

With this method, a biological environment was mimicked by the ECM protein coating (e.g., Collagen I) to create an accurate in vitro environment for NCCs to grow and survive²⁰^,²¹. The stiffness of the prepared hydrogels was quantitatively analyzed via atomic force microscopy (AFM), a well-known technique to depict the elastic modulus²⁶. To study the effect of different stiffness levels on NCCs, wild-type O9-1 cells were cultured and prepared on hydrogels for immunofluorescence (IF) staining against filamentous actin (F-actin) to show the differences in cell adhesion and morphologies in response to changes in substrate stiffness. Utilizing this in vitro system, researchers will be able to study the roles of mechanical signaling in NCCs and its interaction with other chemical signals to gain a deeper understanding of the relationship between NCCs and mechanical signaling.

Protocol

1. Hydrogel preparation

NOTE: All steps must be performed in a cell culture hood that has been disinfected with ethanol and ultraviolet (UV)-sterilized before use to maintain sterility. Tools, such as tweezers and pipettes, must be sprayed with ethanol. Buffer solutions must also be sterile-filtered.

Preparation of aminosilane-coated glass coverslips
1. Place the desired number of glass coverslips onto a piece of laboratory wipe.
  NOTE: Prepare an additional 3-4 coverslips to ensure sufficient backup supplies as they break easily. Different materials of glass coverslips will yield different compatibility of cell seeding and attachment. It is better to determine which type suits the experiment best before starting the experiments (see the Table of Materials).
2. Use an alcohol burner or Bunsen burner to sterilize each coverslip by passing it back and forth through the flame (30 s for protein assay experiments). Place each glass coverslip on a laboratory wipe to cool down.
3. Once the glass coverslips are cooled down, transfer them onto a Petri dish lined with parafilm to prevent slippage.
  NOTE: If the coverslips are not cool enough, the residual heat will melt the parafilm onto the slips, rendering them unusable.
4. Cover the coverslips with approximately 200 μL and 800 μL of 0.1 M NaOH for a 12 mm and a 25 mm coverslip, respectively, and let them sit for 5 min. Then, aspirate the 0.1 M NaOH and allow the coverslips to air-dry for another 5 min to form an even film.
5. Once the coverslips are dried, pipette approximately 80 μL and 150 μL of 3-aminopropyl triethoxysilane (APTS) for 12 mm and 25 mm coverslips, respectively. Be careful to avoid spilling the solution onto the parafilm. Allow the solution to sit for 5 min.
6. Aspirate as much excess APTS as possible and allow the residual APTS to dry for 5 min. Rinse the coverslips well by submerging them in sterile, deionized (DI) H₂O three times for 5 min each time.
  NOTE: If the glass coverslips are not rinsed well, the residual APTS causes unwanted reactions with glutaraldehyde, causing a white precipitate to form and resulting in unusable coverslips.
7. Move the coverslips to a new Petri dish with the reactive side facing up. Add enough 0.5% glutaraldehyde to the Petri dish to cover the coverslips entirely and allow the coverslips to sit for 30 min.
8. Aspirate the 0.5% glutaraldehyde and rinse the coverslips again in DI H₂O one time for 3 min. Set the coverslips reactive side up on a laboratory wipe or a clean Petri dish to air-dry completely before using.
  NOTE: The protocol can be paused here; coverslips must be placed in sterile DI H₂O until use.
Preparation of siliconized coverslips
1. Place the same number of coverslips as the aminosilane-coated coverslips (step 1.1.1) in a Petri dish lined with parafilm.
2. Pipette 40 μL or 150 μL for 12 mm and 25 mm coverslips, respectively, of dichloromethylsilane (DCMS) to one side of the coverslip and allow the solution to sit for 5 min.
3. Aspirate any remaining solution from the coverslip, wash in sterile DI H₂O once for 1 min, and place the reactive coverslips face up on a laboratory wipe to air-dry completely before moving onto the next step.
Preparing hydrogels
1. Mix acrylamide, bis-acrylamide, and DI H₂O in a 1.5 mL centrifuge tube to prepare 500 μL of solutions with varying stiffnesses (see Table 1). Vortex the solution for 30 s to mix it thoroughly.
2. Working swiftly, add the 10% ammonium persulfate solution (APS) and tetramethylethylenediamine (TEMED) to the tube and vortex the solutions again to mix the solutions.
  NOTE: Prepare fresh 10% APS and leave it on ice or freeze into single-use aliquots due to its sensitive freeze/thaw cycle.
3. Pipette approximately 33 μL or 100 μL of the solution onto the dried 12 mm or 25 mm aminosilane-coated coverslips (section 1.1), respectively.
4. Using curved tweezers, immediately place the DCMS-treated coverslip on top of the gel solution with the treated side touching the gel solution, thus sandwiching the gel solution between the DCMS-treated coverslip and aminosilane-coated coverslip.
5. Allow the gel solution to polymerize for 5-15 min, while actively monitoring for gel polymerization of the leftover solution in the tube.
6. Once the gel is polymerized, separate the DCMS-treated coverslip with curved tweezers or a razor blade, leaving the gel attached to the original aminosilane-coated coverslip.
7. Immediately place the coverslip with the attached hydrogel in a predetermined 4-well/24-well and 6-well plate covered with 500 µL and 2 mL of sterile PBS or DI H₂O for 12 mm and 25 mm coverslips, respectively, to prevent the gel from drying out.
8. Repeat steps 1.3.4-1.3.7 for all coverslips.
9. Submerge the hydrogels in sterile PBS or DI H₂O for 30 min to remove excess acrylamide solution. Store the hydrogels in sterile PBS or DI H₂O at 4 °C for a procedural stop here.
10. In a dark room, prepare the sulfosuccinimidyl 6-(4'-azido-2'-nitrophenylamino) hexanoate (sulfo-SANPAH) mixture by mixing 2.5 mL of 50 mM 2-[4-(2-hydroxyethyl) piperazin-1-yl] ethanesulfonic acid(HEPES) (pH=8.5) with 25 μL of the 50 μg/mL sulfo-SANPAH in a conical tube, wrapped in aluminum foil to protect from light. Use a pipette to mix the solution well before using.
  NOTE: A volume of 2.5 mL of sulfo-SANPAH solution is enough for approximately twenty-five 12 mm hydrogels or five 25 mm hydrogels.
11. Aspirate PBS or DI H₂O from the well plate. Add approximately 100 μL or 500 μL for 12 mm and 25 mm coverslips, respectively, of sulfo-SANPAH solution (step 1.3.10) to cover the gel. Ensure the solution covers the gel entirely.
  NOTE: Adjust the vacuum suction strength to prevent the strong force from ripping or disturbing the hydrogels.
12. Place the gels with the solution under a 15 W, 365 nm UV light for 10 min, uncovered to minimize any interference of the UV light reacting with the sulfo-SANPAH.
13. Aspirate the excess sulfo-SANPAH by tilting the plate to collect as much of the solution as possible. Wash the gel with 50 mM HEPES two to three times.
14. Add 500 μL and 2 mL for 12 mm and 25 mm gels, respectively, of 50 mg/mL collagen I diluted in 0.2% acetic acid to each well containing the hydrogel. Allow the gels to incubate overnight in a 37 °C, 5% CO₂ incubator.
  NOTE: Dilute collagen I in 0.2% acetic acid instead of 50 mM HEPES to promote homogenous distribution and attachment of collagen I.
15. Aspirate the collagen I and wash the gels with sterile PBS three times to remove excess collagen I for 5 min each wash. Incubate the hydrogels in PBS with 10% horse serum, 5% FBS for 2 h in the 37 °C, 5% CO₂ incubator.
  NOTE: The addition of 10% horse serum promotes higher proliferation compared to only using FBS as done in the previous publication.
16. Aspirate the medium. Add 500 mL of sterile-filtered Dulbecco's Modified Eagle Medium (DMEM) with 10% FBS and 1% penicillin-streptomycin (P/S) to each well. Store the gels in the 37 °C, 5% CO₂ incubator until ready for cell culture.
17. Once ready, plate approximately 1.5 × 10⁴ O9-1 cells/cm² in basal medium in the culture dishes. Incubate the cells for 2 days in an incubator at 37 °C, 5% CO₂. Check the cells for confluency to ensure that the cells are sufficiently attached to gels, and that the number of cells is enough before collecting for analysis.
  NOTE: See the previously published protocol for the steps of recovery, passage, and collection of O9-1 cells²⁰.
18. Proceed to sections 2, 3, or 4 for further analysis of the hydrogels.

2. Quantitative analysis of stiffness via AFM

Start the AFM system computer, followed by the AFM controller (see the Table of Materials).
Mount the AFM cantilever on the AFM probe holder. Use a spherical cantilever with a 0.5 μm silica bead mounted at the end of the cantilever (cantilever with spherical bead).
NOTE: For stiffer hydrogels, such as 10 kPa, 20 kPa, and 40 kPa, a stiffer probe was used with the spring constant of 0.24 N/m. A softer probe was used for softer hydrogels, such as 0.5 kPa and 1 kPa, with a spring constant of 0.059 N/m.
Set the AFM software under contact mode.
Mount the silicon wafer onto the AFM sample stage to collect force curves by clicking on Engage for the cantilever to touch the silicon substrate, thus generating the force curves.
Use the force curves above (2.4) for calibration, click on Calibrate in the controlling software to obtain an average spring constant of the cantilever under thermal tune condition, and save the calibrated values in the controlling software.
Mount the samples by placing the coverslip with the attached hydrogel in a 60 mm Petri dish onto the AFM scanning stage. Add 3 mL of PBS into the dish before conducting measurements to prevent the gel from drying out.
Set the AFM to work in contact mode (fluid) to start measurement. Engage the spherical bead to continuously touch and lift from the gel sample.
Set the cantilever so that its deflection threshold remains at 10 nm. Keep the ramping size of the probe at 10 μm. Then, record the force curves as in step 2.4.
Acquire at least 20 force curves from at least 3 to 10 different spots across the surface of the hydrogel.
Calculate the average Young's modulus of ~20 force curves for each spot with AFM imaging and analysis software. Use extend ramp force curves and a linearized model (spherical). Calculate the average of all spots for each sample to yield the final stiffness.
NOTE: Young's modulus and related data (i.e., standard deviations) are automatically saved as a spreadsheet.
Repeat steps 2.6-2.10 for all samples.

3. Molecular analysis of stiffness via immunofluorescence staining

Use tweezers to transport the coverslip to a new plate to minimize false signals from cells grown directly onto the plate. Wash the cells with 500 µL of sterile PBS three times to remove dead cells and any remaining culture medium.
Fix the cells using 500 µL of 4% paraformaldehyde (PFA) for 10 min at room temperature, undisturbed. Then, rewash the cells three times using 500 µL of PBS/well for 2 min each.
NOTE: Store at 4 °C for a procedural stop.
Treat the cells with 500 µL of 0.1% Triton X-100 for 15 min at room temperature. Then, wash the cells three times with 500 µL of PBS/well.
Block the cells with 250 µL of 10% donkey serum (diluted in PBS and 0.1% Tween 20) per well for 30 min at room temperature.
Incubate the cells with 250 µL of primary antibodies for 2 h at room temperature or overnight at 4 °C. Then, wash the cells three times with 500 µL of PBS/well for 5 min each.
NOTE: Anti-Vinculin (Vcl) (1:250) and anti-AP2 alpha (1:250) were used in this experiment and were diluted in 10% donkey serum.
Incubate the cells with corresponding secondary antibodies and/or phalloidin used for F-actin staining at a dilution of 1:400 in 250 µL of 10% donkey serum for 30 min at room temperature. Then, wash the cells three times with PBS for 5 min each.
NOTE: 568 nm Phalloidin can be co-incubated with 488 nm or 647 nm secondary antibodies or on its own.
Incubate the cells with 4′,6-diamidino-2-phenylindole (DAPI, 1:1000 dilution) in 250 µL of PBS for 10 min followed by one last wash of PBS for 2 min.
Add 3-4 drops of mounting medium to each well. Store the samples at 4 °C to set for at least 2 h before imaging to ensure the mounting medium has set properly.
Capture images of at least 3 random frames per hydrogel sample with a fluorescence microscope, producing individual and merged channels.

4. Quantitative real-time PCR (RT-qPCR)

Transfer the hydrogels with the adherent cells for RNA collection to a new plate to minimize unwanted RNA from cells attached to the cell plate. Wash the cells with PBS three times to remove dead cells and culture medium.
Extract the total mRNA using an RNA extraction kit. Perform reverse-transcription of RNA to cDNA using a reverse transcription supermix following the manufacturer's instructions.
Perform RT-qPCR with primers for Vcl as the stiffness marker of choice and analyze using the 2^-ΔΔCT method.
NOTE: Primer sequence of Vcl: Forward 5' GCTTCAGTCAGACCCATACTCG 3'; reverse 5' AGGTAAGCAGTAGGTCAGATGT 3'.

Representative Results

Hydrogel preparation and stiffness assessment through AFM and the Hertz model
Here, a detailed protocol is provided to generate polyacrylamide hydrogels of varying stiffness by regulating the ratio of acrylamide and bis-acrylamide. However, the polyacrylamide hydrogels are not ready for the adhesion of cells due to the lack of ECM proteins. Thus, sulfo-SANPAH, acting as a linker, covalently binds to the hydrogels and reacts with the primary amines of ECM proteins to allow the adhesion of ECM proteins to the surfaces of the hydrogels via the N-hydroxysuccinimide ester in sulfo-SANPAH after UV activation. Collagen type I was used as the ECM protein of choice to effectively promote O9-1 cell attachment. To ensure accurate stiffness values of different hydrogels, a stiffness assessment was performed using AFM, a well-known technique to depict the elastic modulus.

Upon successful formation and attachment of the polyacrylamide hydrogel to the glass coverslip, the gel remained adherent to the coverslip with an even surface and minimal tearing. The stiffness was measured by AFM based on the principle of indention technique, wherein a stiff indenter was applied to the sample with the required force to reach an indentation depth²⁶. With this measurement, the Young's elastic modulus was calculated based upon the indentation of depth and force in Hertz's model, an elastic theory²⁶. However, due to the large variation in results by AFM, an additional statistical method was applied to obtain a quantitative result with minimal impact of uneven surfaces and imperfect homogeneity of the gel solutions²⁶. To produce a quantitative measurement using AFM, a compilation of at least 50 force and distance curves from each location on the gel sample was taken for an average sample stiffness. The force applied to the high-stiffness gel was higher than that applied to the softer gel, indicating that a stiffer substrate yielded a steeper slope in the Force vs. Z graph, in which force is measured in nN, and Z indicates the indentation depth between the indenter and sample.

On soft hydrogels, the slope of the generated force curve was gentle as the required force from the AFM probe was less (Figure 1A). However, on stiff hydrogels, such as those with the modulus of 40 kPa, the generated slope was much steeper as the applied force was higher than for softer gels (Figure 1B). As the separation between the probe and the hydrogel sample decreases, the curve increases significantly as the tip of the probe touches the glass coverslip. However, as the separation distance increases, the curve merely approaches 0 as there is no applied force present.

As shown in Figure 1A, the cantilever on the AFM probe approached the gel, indicated by the blue line, and the probe measured the applied force required to penetrate the gel sample and eventually reach the glass coverslip, causing a sudden increase in force. Due to possible procedural and instrumental errors, such as the quality of the required solutions, the true stiffness of hydrogel samples varies largely and far from the desired stiffness. Thus, AFM is a useful tool to validate and confirm the methodology while preventing false data presentation in further experiments.

In this AFM assessment, the five prepared hydrogel samples were measured through the quantitative approach. The protocol focused on hydrogel stiffness levels of 0.5 kPa, 1 kPa, 10 kPa, 20 kPa, and 40 kPa, which mimic the breadth of biological substrate stiffness levels reported for differentiation of various cell types. The force curves obtained from AFM measurements were utilized to generate the Young's elastic modulus in kilopascals using an AFM analysis algorithm software (Figure 2).

Comparison of polyacrylamide hydrogel systems and cell types
This adaptation of the original protocol by Tse and colleagues provides an efficient and effective approach to study the mechanosensitive aspects of NCC using O9-1 cells²⁰. Modifications to the previous protocol include modifying ECM protein incubation: replacing 50 mM HEPES with 0.2% acetic acid and the addition of 10% horse serum and FBS for cell culture (step 1.3.14-1.3.15). These modifications were validated by comparing the growth and maintenance of O9-1 NCCs on this modified gel system with that in the original (control) protocol. Here, we cultured wild-type O9-1 cells on both hydrogel systems with the elastic modulus of 1 kPa and 40 kPa for each system in basal medium. The overall cell growth status and development were visualized using a brightfield light microscope for apoptotic characteristics, stressed morphology, and cell attachment to the hydrogels. O9-1 cells grown on the original gel system resulted in a higher number of dead cells indicated by an excess of round cells (Figure 3E,F) for both 1 kPa and 40 kPa hydrogels.

In contrast, the O9-1 cells grown on the modified gel system exhibited healthy cell growth and sufficient attachment to the hydrogel substrate (Figure 3G,H). In addition, the compatibility of NCCs with the modified hydrogel system was assessed by performing IF staining of the NCC marker, Tcfap2α (AP-2). AP-2 is a transcription factor expressed in the NC lineages to regulate development in mouse embryos, thus making it suitable to assess compatibility²⁷. Although O9-1 cells grown on control and modified hydrogel systems both expressed AP-2, there was a significant increase in AP-2 expression in O9-1 cells plated on the modified hydrogel system, as indicated by the stronger fluorescence signal and the corresponding quantification (Figure 4A,B).

In addition, P19 cells were used to further validate the benefits of the modified hydrogel system for the growth of cells. P19 is an embryonic carcinoma cell line that was derived from embryo-derived teratocarcinoma in mouse²⁸. Using the corresponding culture protocol, P19 cells were grown on both control and modified hydrogel systems to monitor survival and growth characteristics. Brightfield imaging revealed that P19 cells plated on both hydrogel systems displayed an excess of round floating cells and a lack of cell-substrate attachments (Figure 3A–D). This observation suggested that the modified protocol was more suitable for O9-1 NCCs to study mechanical signaling in NCCs.

Visualization of high-stress fiber expression on stiff substrates
The modified hydrogel allowed for quantitative and qualitative analysis of the differences in the morphology of cells cultured on gels of different stiffness levels and other effectors. Once the hydrogels were ready for cell seeding, wild-type O9-1 cells were passaged onto hydrogels of different stiffness levels. Cells were monitored for their health and growth by observing their shape, spatial spread, and even attachment on the hydrogel with minimal dead cells. Some studies have shown an increase in stress fibers and cell adhesion for MSCs on high-stiffness substrates, suggesting that NCCs grown on a stiffer substrate would also exhibit similar findings compared to NCCs grown on softer substrates²⁹^,³⁰.

F-actin along with myosin II, α-actinin, and other cytoskeletal proteins are known collectively as stress fibers³¹. Previous studies observed an increase in stress fiber assembly in response to increased mechanical force³¹. At one or both ends of the stress fibers, attachments to the focal adhesion complex enable cells to migrate and adhere to the ECM³¹. Phalloidin staining to visualize F-actin expression and organization in the NCCs demonstrated healthy cell growth in response to mechanical signaling (Figure 5). Additionally, the O9-1 cells grown on low- or high-stiffness hydrogels exhibited different morphologies through varying amounts of stress fibers (Figure 5). Similar to observations from reported studies performed using MSCs, it was observed that O9-1 cells grown on a stiffer substrate, 40 kPa, exhibited more stress fibers and were well-spread compared to cells grown on a softer hydrogel, indicated by 1 kPa stiffness²⁹^,³⁰.

Assessment of cell adhesions
To further confirm the hypothesis that the change in substrate stiffness impacts NCC adhesion, changes in Vcl expression were quantitatively measured via RT-qPCR in NCCs responding to different hydrogel stiffness levels. Vcl is one of the numerous cytoskeletal proteins present in the focal adhesion complex during the process of the cell establishing contacts with the substrate and sensing the ECM properties³². Focal adhesions are the contact points of the cells to the ECM via integrin receptors, which anchor to the cytoplasmic actin cytoskeleton, F-actin³³ The Vcl gene expression level suggests the changes in focal adhesions and cell adhesions of the O9-1 cells in response to the substrate stiffness.

Previous studies showed the effect of Vcl on cell adhesion in embryonic stem and fibroblast cells by differences in its expression. In response to the high expression of Vcl, the number and sizes of focal adhesions also increased but decreased when Vcl was knocked down³⁴. Consistently, Vcl-deficient cells also showed a significant decrease in cell adhesion and spreading³⁵. In addition, Vcl plays a role in regulating cell adhesion by stabilizing focal adhesions³⁶. The size of focal adhesions, maturation level, and compositions vary according to the substrate stiffness, thus allowing signals to be transduced intracellularly and the cells to respond to their environmental cues³⁷. Thus, Vcl is highly recruited to the focal adhesion complexes in cells grown on stiff substrates, as reflected by higher mRNA levels detected by RT-qPCR (Figure 6C).

Cells grown on softer substrates form minimal focal adhesion complexes, as reflected by lower mRNA levels of Vcl in the cells¹⁵. In Figure 6C, O9-1 cells exhibited a higher expression of Vcl on the stiff substrate than on the soft substrate. These results suggest a higher level of cell-substrate adhesions of O9-1 cells on stiff substrates than O9-1 cells on softer substrates. In addition, Vcl expression was qualitatively visualized through IF staining with an anti-Vcl antibody to further complement and support the RT-qPCR finding. Consistently, the Vcl expression in O9-1 cells grown on the stiffer substrate was higher than those grown on the softer substrate (Figure 6A,B), which further supported the initial finding of high cell adhesion and spreading on the 40 kPa hydrogel in comparison to the 1 kPa hydrogel observed with F-actin phalloidin staining and Vcl expression levels via RT-qPCR.

Figure 1: Force curves generated from the indentation of the AFM probe. Force (y-axis) indicates the required force applied in nN, and Z (x-axis) indicates the Bruker AFM probe distance from the sample in µm. For the 1 kPa hydrogel (A), the generated slope is gentle vs. the steeper slope observed for the 40 kPa hydrogel (B). The colored curves represent the movement of the cantilever on the AFM probe as it approaches (blue) and retracts (red) from the hydrogel sample. The highest starting point of the curve indicates the rigid contact of the glass coverslip. (B) The large dip in the retracted curve in the 40 kPa hydrogel indicates adhesion between the bead and the sample. Abbreviation: AFM = atomic force microscopy. Please click here to view a larger version of this figure.

Figure 2: The average stiffness of hydrogels (in kPa) calculated from the Young's elastic modulus. The Young's modulus was generated from the force curves from Figure 1. The referenced elastic moduli of the hydrogels were 0.5 kPa, 1 kPa, 10 kPa, 20 kPa, and 40 kPa. Error bars indicate standard deviation. Please click here to view a larger version of this figure.

Figure 3: Bright-field images of P19 and O9-1 cells plated on 1 kPa and 40 kPa hydrogels of control and modified gel systems to detect cell growth characteristics. (A–D) P19 and (E–H) O9-1 cells; dead cells are indicated by red arrows. Scale bars = 25 µm. Please click here to view a larger version of this figure.

Figure 4: Immunofluorescence staining of NCC marker AP-2 in O9-1 NCCs to visualize NCC compatibility. (A) A 40 kPa modified hydrogel system compared to (B) a 40 kPa control. AP-2 (green); nuclei were stained with DAPI (blue). Scale bars = 25 µm. (C) Bar graph provides quantification of the AP-2 expression level showing significance (p-value = 0.003) (n = 3). Data show the relative expression with provided standard deviation error bars. Abbreviations: NCC = neural crest cell; DAPI = 4′,6-diamidino-2-phenylindole. Please click here to view a larger version of this figure.

Figure 5: Fluorescent phalloidin staining of F-actin showing stress fibers that are well-spread out in O9-1 cells on the 40 kPa hydrogel. O9-1 cells were cultured on 1 kPa (A) and 40 kPa hydrogels (B). O9-1 cells were stained using Alexa Fluor 488 Phalloidin (green), and the nuclei were stained with DAPI (blue). Scale bars = 25 µm. Abbreviation: DAPI = 4′,6-diamidino-2-phenylindole. Please click here to view a larger version of this figure.

Figure 6: Immunofluorescence images of vinculin in O9-1 cells. O9-1 cells were plated on 1 kPa (A) and 40 kPa (B) hydrogels. Nuclei were stained with DAPI (blue). Scale bars = 25 µm. (C) Real-time quantitative PCR analysis of the total mRNA level of Vcl in O9-1 cells cultured on 1 kPa and 40 kPa hydrogels. Vcl expression level on the 1 kPa hydrogel is significantly lower than that on the 40 kPa hydrogel (p-value = 0.02). Data shows the average with provided standard deviation error bars. Abbreviation: DAPI = 4′,6-diamidino-2-phenylindole. Please click here to view a larger version of this figure.

500 μL total volume	0.5 kPa	1 kPa	10 kPa	20 kPa	40 kPa
40% Acrylamide (μL)	37.5	62.5	125	100	100
20% Bis-acrylamide (μL)	15	7.5	25	66	120
H₂O (μL)	447.5	430	350	334	280
10% APS (μL)	5	5	5	5	5
TEMED (μL)	0.5	0.5	0.5	0.5	0.5

Table 1: Corresponding volumes of solutions to obtain the desired stiffness levels.

Discussion

The goal of the current study is to provide an effective and efficient in vitro system to better understand the impact of mechanical signals in NCCs. In addition to following the step-by-step protocol mentioned above, researchers need to keep in mind that the cell culture of O9-1 NCCs is affected by the type of glass coverslips used to prepare hydrogels. For instance, it was noted that cells seeded on a specific type of glass coverslip (see the Table of Materials) survived and proliferated well, while cultured cells seeded on other types of glass coverslips showed more cell death. Furthermore, it is important to strictly follow the correct cell culture conditions for O9-1 NCCs³⁸. The quality of the cell culture is optimal when the hydrogels are used as soon as possible or stored in a sterile 37 °C incubator for up to two days.

Due to the sensitivity of each component in the protocol, the elastic moduli could vary across experiments. In addition to the points mentioned in the protocol (step 1.3.2) regarding 10% APS, other critical factors to keep in mind also affect the variation. Another factor that was suspected of causing large variations in AFM measurements was the thickness of the hydrogels. A previous study had investigated the effect of thickness on the Young's moduli, ranging from 15 to 1000 µm, and had found that differences in thickness did not change the Young's moduli significantly³⁹. However, the thickness of the substrates also affects the mechanical properties that the cells can sense, leading to different morphologies⁴⁰^,⁴¹^,⁴². Various studies showed that a significant increase in the thickness of hydrogels led to a decrease in the cell area, spreading, and effective stiffness of hydrogels⁴⁰^,⁴¹^,⁴². However, the phenotypes of cells also change in response to significantly thin hydrogels, e.g., higher spreading even on low-stiffness hydrogels⁴⁰^,⁴¹^,⁴². With a consistent volume of polyacrylamide gels, the thickness of hydrogels should be uniform so that slight deviations will not significantly affect the elastic modulus in AFM measurements.

It is better to sterilize coverslips by passing them back and forth in the flame using an alcohol burner because other sterilization methods can be more complicated and cause potential damage to the glass coverslips. Different sizes of glass coverslips can be used based on experimental requirements. This protocol utilized 12 mm and 25 mm coverslips for immunohistochemistry and RT-qPCR, respectively. Using appropriately sized gels to suit the experiments encourages efficiency and minimizes waste. These modifications were validated qualitatively and quantitatively to ensure optimization for O9-1 NCCs compared to the original (control) hydrogel system²⁰. The overall health and growth of O9-1 NCCs were assessed under a brightfield microscope for cellular and substrate attachment characteristics.

In addition, the compatibility of O9-1 cells was compared between both control and the modified hydrogel systems to further validate the modifications in this protocol by qualitatively visualizing AP-2 expression using IF staining. The intensity of the signals was quantified to further support the representative images of AP-2 expression in O9-1 cells between control vs. the modified hydrogel systems. While AP-2 is a common NCC marker, other well-known markers must be considered for validation, such as Sox10 and Pax3, due to their significance for NCC maintenance of pluripotency and survival²⁸. In addition, the optimization in this protocol was further confirmed by comparing the O9-1 NC cells with another cell line, P19, to ensure that this hydrogel system is efficient and reliable for NC cells. Although P19 cells have immortal characteristics and are easily cultured, they did not thrive well on either of the hydrogel systems.

The resistance to the elongating force generated from the substrate or tissue stiffness where the cells attach is often expressed as Young's elastic modulus⁴⁵. With AFM, the Young's elastic modulus is obtained from the force curve generated from the applied vertical force²⁶. Large variations can occur during AFM measurement, between measurements that can lead to inaccurate readings for the stiffer hydrogels. The inconsistency can be caused by improper probes used for measurement. For instance, measurement of 20 kPa and 40 kPa hydrogels require the use of a stiffer probe with a higher spring constant (k = 0.24 N/m). A stiffer probe allows for a lower resolution compared to a softer probe; however, there are reasons to favor the choice of a stiffer probe as too-soft cantilevers could adhere to the samples⁴⁶. In addition, too-soft probes are highly sensitive, contributing to false signals from unwanted particles and resulting in artificially lower or higher stiffness values than the true stiffness⁴⁶. Furthermore, accurate input of Poisson's ratio must be noted, depending on the measuring material; this could be found in standardized studies as this significantly affects the data output.

In addition, AFM was utilized to measure the thickness of the hydrogels, as thickness is another mechanical property affecting how cells sense their environment⁴⁷^,⁴². In various reported studies, cells that are grown on soft hydrogels are observed to be round in shape at and beyond "critical thickness," which is reported at ~2-5 μm, depending on the cell type⁴⁷^,⁴²^,⁴⁸. However, much higher spreading was observed when cells were plated on hydrogels of the same stiffness but lower thickness than the "critical thickness"⁴²^,⁴⁸. A potential explanation for this interesting finding is that the sub-critical thickness of hydrogels enables the cells to sense the rigid underlying glass coverslips as the cells exert traction for lateral displacement⁴⁷. The average thickness across all-stiffness hydrogels was 342 μm with a standard deviation of 27 μm. The thickness of the hydrogels was higher than the suggested "critical thickness", and within the testing range of under 400 μm, which was reported in studies and the manufactured premade hydrogels, such that the cells could sense the different stiffness of the hydrogels and not the underlying rigid glass coverslips⁴²^,⁴⁸.

In addition to the AFM quantitative analysis method, the hydrogels were also qualitatively analyzed through immunohistochemistry to study the expression of the markers affected by the varying stiffness in O9-1 cells and to visualize healthy growth of the cells. F-actin in the cytoplasm is connected to the membrane-bound integrins via a set of cytoskeletal proteins, such as talin and Vcl, forming the focal adhesion complex³³. Expression of stress fibers in cells could also be analyzed by measuring the expression of other cytoskeletal genes in cells, such as talin and integrin, which could be visualized together using the focal adhesion staining kit.

There were varying degrees of hydrogel stiffness that influenced NCC morphology and response, as seen in the change in cell adhesion and stress fibers through mechanical signaling. This protocol offers the ability to influence cell differentiation into various cell types by modifying the corresponding culture conditions in vitro, thus providing a convenient method of manipulation of mechanical signals and chemical signals in NCCs. As mentioned previously, the fate of NCC differentiation is largely guided by mechanical forces present in the surrounding tissue, including its stiffness²^,³. While the immediate goal of this paper was to develop a step-by-step protocol to prepare hydrogels for NCC culture, the potential benefits of this protocol extend beyond the methodology, pursuing further knowledge of mechanical signaling in NCCs. It is also worth noting that this in vitro system has some limitations. This technique of fabricating hydrogels comprises multiple steps that can potentially introduce technical variations along the way, including heterogeneity, uneven surface, and inaccurate stiffness. Therefore, users must perform these steps carefully to minimize technical variations during experiments. In addition, polyacrylamide gels in this system limited studies to 2D culture due to the toxicity of acrylamide, ignoring the precise 3D biological environment that NCCs inhabit⁵⁰.

Despite these constraints, this in vitro system allows for an inexpensive and simple method benefiting all levels of research and enabling researchers to perform sufficient and functional downstream tests. As seen in recent findings, NCCs rely heavily on both mechanical signaling, such as shear force and substrate stiffness, and chemical signaling, such as Wnt and fibroblast growth factor signaling, in craniofacial, as well as heart development in vertebrates⁶^,¹⁵. Using this protocol, the local microenvironments for in vitro experiments can be easily mimicked for future studies on NCCs, including differentiation, migration, cellular responses, and the potential of detrimental disease progression. Therefore, this in vitro system will be a powerful tool to study the roles of mechanical signaling in NCCs and their interactions with other signaling pathways, which will deepen the understanding of the molecular and genetic mechanisms of NCC development and related diseases.

Disclosures

The authors have nothing to disclose.

Acknowledgements

We thank Dr. Ana-Maria Zaske, operator of Atomic Force Microscope-UT Core facility at the University of Texas Health Sciences Center, for the contributed expertise in AFM in this project. We also thank the funding sources from the National Institutes of Health (K01DE026561, R03DE025873, R01DE029014, R56HL142704, and R01HL142704 to J. Wang).

Materials

12 mm #1 Corning 0211 Glass Coverslip	Chemglass Life Sciences	CLS-1763-012
2% Bis-Acrylamide	Sigma Aldrich	M1533
24-well plate	Greiner Bio-one	662165
25 mm #1 Corning 0211 Glass Coverslip	Chemglass Life Sciences	CLS-1763-025
3-aminopropyl triethoxysilane (APTS)	Sigma Aldrich	A3648
4-well cell culture plate	Thermo Scientific	179830
4% Paraformaldehyde	Sigma Aldrich	J61899-AP
40% Acrylamide	Sigma Aldrich	A4058
50% glutaraldehyde	Sigma Aldrich	G7651
6-well cell culture plate	Greiner Bio-one	657160
AFM cantilever (spherical bead)	Novascan
AFM software	Catalyst NanoScope		Model: 8.15 SR3R1
Alexa Fluor 488 Phalloidin	Thermo Fisher	A12379
Ammonium Persulfate (APS)	Sigma Aldrich	248614	Powder
anti-AP-2α Antibody	Santa Cruz	sc-12726
anti-Vinculin antibody	Abcam	ab129002
Atomic Force Microscopy (AFM) Bioscope Catalyst	Bruker Corporation
Collagen type I (100mg)	Corning	354236
DAPI (4',6-Diamidino-2-Phenylindole, Dihydrochloride)	Thermo Fisher	D1306
Dichloromethylsilane (DCMS)	Sigma Aldrich	440272
Donkey serum	Sigma Aldrich	D9663
Dulbecco's Modified Eagle Medium (DMEM)	Corning	10-017-CV
Fetal bovine serum (FBS)	Corning	35-010-CV
Fluorescence microscope	Leica		Model DMi8
Fluoromount-G mounting medium	SouthernBiotech	0100-35
HEPES	Sigma Aldrich	H3375	Powder
Horse serum	Corning	35-030-CI
iScript Reverse Transcription Supermix	Bio-Rad	1708841
Penicillin-Streptomycin antibiotic	Thermo Fisher	15140148
RNeasy micro kit	Qiagen	74004
Sterile 1x PBS	Hyclone	SH30256.02
Sterile deionized water	Hardy Diagnostics	U284
sulfo-SANPAH	Thermo Fisher	22589
SYBR green	Applied Biosystems	4472908
TEMED	Sigma Aldrich	T9281
Triton X-100	Sigma Aldrich	X100
Tween 20	Sigma Aldrich	P9416

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Le, T. P., Zhao, X., Erhardt, S., Gu, J., Wang, H., Findley, T. O., Wang, J. An Optimized O9-1/Hydrogel System for Studying Mechanical Signals in Neural Crest Cells. J. Vis. Exp. (174), e62693, doi:10.3791/62693 (2021).