Evaluation of Keratinocyte Proliferation on Two- and Three-dimensional Type I Collagen Substrates

Hitomi Fujisaki; Sugiko Futaki; Kazunori Mizuno; Shunji Hattori

doi:10.3791/59339

JoVE Journal > Bioengineering

Bioingeniería

Evaluation of Keratinocyte Proliferation on Two- and Three-dimensional Type I Collagen Substrates

Published: April 22, 2019

doi:

10.3791/59339

Hitomi Fujisaki¹, Sugiko Futaki², Kazunori Mizuno¹, Shunji Hattori¹

¹Nippi Research Institute of Biomatrix, ²Department of Anatomy and Cell Biology,Osaka Medical College

Summary

Here, we present a protocol for the preparation of two different forms of culture substrates utilizing type I collagen. Depending on how collagen is handled, collagen molecules either maintain two-dimensional, non-fibrous form or reassemble into three-dimensional, fibril form. Cell proliferation on type I collagen is drastically affected by fibril formation.

Abstract

Type I collagen, useful as a substrate for cell culture, exists in two forms: the two-dimensional, non-fibrous form and three-dimensional, fibril form. Both forms can be prepared with the same type I collagen. In general, the non-fibrous form promotes cell adhesion and proliferation. The fibril form (gels) provides more physiological conditions in many types of cells; therefore, gel culture is useful for examining physiological behaviors of cells, such as drug efficacy.

Researchers can select the appropriate form according to the purpose of its use. For example, in the case of keratinocytes, on-gel culture has been used as a wound healing model. FEPE1L-8, a keratinocyte cell line cultured on the non-fibrous form of type I collagen, promote cell adhesion. Notably, keratinocyte proliferation is slower on the fibril form than the non-fibrous form. Protocols for the preparation of type I collagen for cell culture are simple and have wide applications depending on the experimental needs.

Introduction

Interstitial connective tissues comprise a three-dimensional protein meshwork of heterogeneous composition, primarily composed of type I collagen fibrils¹. Collagen fibrils play a key role as a scaffold for cells¹^,²^,³ and interact with other extracellular matrix (ECM) proteins³. In vitro, different forms of type I collagen can be used as substrates for cell culture depending on the handling method¹^,²^,³^,⁴. Under acidic conditions, type I collagen maintains the non-fibrous form⁵. Coating the surface of culture dishes with the non-fibrous form promotes cell adhesion and proliferation⁶^,⁷. At physiological pH and temperature, type I collagen molecules reassemble into fibrils that form gels possessing a three-dimensional structure¹^,²^,³^,⁴^,⁵^,⁶^,⁷^,⁸. There are several important differences between the fibril and non-fibrous forms of type I collagen, including matrix stiffness and efficiencies of reconstruction of ECM components by the cells during the culture¹. Matrix stiffness is one of the most studied regulatory factors of cell culture¹^,⁹. However, the complex interactions between substrates and cells remain to be clarified. To examine the complex interactions between cells and environmental factors, a simple system is useful. Comparison of the cellular behavior on the two different forms of collagen may help to simplify the effect of environmental factors. Depending on the purpose of their use, different forms of type I collagen can be selectively used. Normally, keratinocytes are in contact with the basement membrane but not with type I collagen. However, during wound healing, keratinocytes move to the dermal connective tissue, proliferate, and heal the wound¹⁰.

Recently, we demonstrated that the concentration of extracellular calcium is important for proliferation of keratinocyte line cells by using the culture system on the fibril form of type I collagen mimicking the dermal connective tissue¹¹. When the keratinocyte cell line FEPE1L-8 was cultured on the fibril form of type I collagen, the shape of the cells was round and their proliferations were stopped at an extracellular calcium concentration of 30 μM¹¹. When the calcium concentration was increased to 1.8 mM, cell growth was recovered¹¹. The cells grew under both calcium concentrations (30 μM and 1.8 mM) when cultured on the non-fibrous form¹¹, whereas they were more sensitive to the exogenous calcium concentration when cultured on the fibril form. FEPE1L-8 was generated through transfection with the papillomavirus type 16 transforming genes E6 and E7 from human cervical carcinoma, non-tumorigenic, inhibit unlimited proliferation with limited differentiation potential like normal keratinocytes¹²^,¹³. FEPE1L-8 cells can be maintained by using some kinds of keratinocyte specific medium, including K110 Type-II with additive supplement K-1 (K110)⁶. Here, we describe the culture protocol of the human keratinocyte cell line on the non-fibrous and fibril forms of type I collagen.

Protocol

1. Preparation of keratinocyte culture medium

NOTE: Perform all procedures under aseptic conditions.

Add 5 mL of penicillin-streptomycin and 10 mL of additive supplement K-1 to 500 mL of K110 Type-II medium (K110) using a pipette.

2. Preparation of the fibril form of type I collagen

NOTE: Perform procedures until step 2.6 under aseptic conditions.

Keep 10x phosphate-buffered saline (PBS (-)), deionized water, collagen, a 96-well culture plate, and an empty 2-mL tube on ice.
NOTE: Do not use the same plate to prepare the fibril and non-fibrous forms.
Add 1.12 mL of deionized water to an empty 2 mL tube using a pipette. Add 200 µL of 10x PBS (-) to the deionized water in the 2 mL tube using a pipette. Gently shake the tube several times.
Add 0.66 mL of collagen to the 2 mL tube using a pipette. Gently and quickly shake the tube several times.
NOTE: Avoid bubble formation in the solution as much as possible. Prepare collagen solution immediately prior to use.
Pour 100 µL of the collagen solution from step 2.3 into each well of the 96-well culture plate. Gently shake the culture plate in a left to right motion.
NOTE: Cover the entire surface of the wells with the collagen solution. If the solution does not cover the entire surface, spread the solution using a pipette tip. Avoid bubble formation in the solution as much as possible.
Place the culture plate in a CO₂ incubator and incubate at 37 °C for 1 h. Check the gelation of collagen and move the culture plate to a clean bench.
NOTE: Confirm gelation by tilting the culture plate.
Gently pour 150 µL of K110 on the gels using a pipette along the wall of the well, place the culture plate in a CO₂ incubator and incubate at 37 °C for 1 h. Move the culture plate to a clean bench. Prior to cell culture, gently discard the K110 using a pipette.
NOTE: To protect the gels, the tip of the pipette should touch the wall of the well.

3. Preparation of the non-fibrous form of type I collagen

NOTE: Perform all procedures under aseptic conditions.

Add 4 µL of collagen to 1.2 mL of 1 mM hydrochloric acid (HCl) in a 1.5 mL tube and gently mix using a pipette.
NOTE: Prepare collagen immediately prior to use. Keep collagen and HCl chilled until the time of use.
Pour 100 µL of collagen into each well of a 96-well culture plate using a pipette. Gently shake the culture plate in a left to right motion and incubate at room temperature for 1 h.
NOTE: Ensure that the entire surface of the wells is covered with solution.
After the incubation, discard the collagen solution and wash the wells with PBS (-) twice using a pipette.
Pour 150 µL of 1% bovine serum albumin/PBS (-) (1% BSA) to a well of the 96-well culture plate and incubate at room temperature for 1 h. Prior to cell culture, discard the 1% BSA.
NOTE: Ensure that the entire surface of the wells is covered with solution.

4. Culture of FEPE1L-8 cells

NOTE: Perform all procedures under aseptic conditions.

Maintain FEPE1L-8 cells in K110 in a 100 mm culture dish in a CO₂ incubator and incubated at 37 °C and 5% CO₂, to semi-confluency.
Prepare K110, trypsin, and trypsin inhibitor in a water bath at 37 °C.
Carefully remove the medium from the culture dish, add 3 mL of 0.05% trypsin using a pipette, place the dish in a CO₂ incubator and incubate at 37 °C for 5 min. After incubation, check cell detachment from the surface of the culture dish using phase-contrast microscopy at 10x magnification.
NOTE: The morphology of the detached cells becomes round. If the cells spread, incubate for an additional period of 5 min.
Add 3 mL of trypsin inhibitor and collect the detached cells in a 15 mL centrifuge tube using a pipette. Centrifuge the cells in a 15 mL centrifuge tube at 200 x g for 5 min.
Discard the supernatant and re-suspend the pellet in 10 mL of K110 using a pipette. Count the cells using phase-contrast microscopy at 10x magnification and prepare cell concentration at 5.0 x 10⁴ cells/mL by appropriate dilution with K110.
Gently seed 0.1 mL of K110 with cells in each well of the culture plate using a pipette along the wall of the well. Place the culture plate in a CO₂ incubator and incubate at 37 °C for the indicated time (2 h, 1 day, 3 days).
NOTE: To protect the gels, the tip of the pipette should touch the wall of the well.

5. Estimation of the number of viable cells

Incubate K110 in a water bath at 37 °C. Mix 130 µL of tetrazolium salt, 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H tetrazolium, monosodium salt (WST-8), and 1.3 mL of K110 in a 2-mL tube using a pipette.
Move the culture plate to a clean bench and gently discard the K110 using a pipette. Gently wash away non-adherent cells with K110 by using a pipette
Add 110 µL of K110 mixed with WST-8 in each well using a pipette, place the culture plate in a CO₂ incubator and incubate at 37 °C for 2 h.
Move the culture plate to a clean bench, collect 100 µL of the conditioned medium from each well, and move it into a well of another 96-well culture plate. Measure absorbance at a wavelength of 450 nm (OD₄₅₀) using a microplate reader and estimate the number of viable cells.

Representative Results

A schematic representation of the treatment of the surfaces of culture dishes using type I collagen is depicted in Figure 1. Cell morphologies observed on the non-fibrous and fibril forms are presented in the left- and right-side panels of Figure 2, respectively. FEPE1L-8 cells were cultured for 2 h (upper panels) and 3 days (lower panels). In the initial 2 h of culturing, the cells adhered and spread on both forms of collagen (Figure 2, upper panels). Three days after seeding, cells on the non-fibrous form continued to spread and cell numbers increased (Figure 2, lower left panel). In contrast, the cells on the fibril form showed limited spreading (Figure 2, lower right panel). FEPE1L-8 cells continued to proliferate on the non-fibrous form of type I collagen (Figure 3, solid black line, closed black circles) and on the untreated dish surfaces (Figure 3, dotted gray line, closed gray circles). In contrast, cells did not proliferate on the fibril form (Figure 3, dotted line, open circles). Figure 2 and Figure 3 have been modified from Fujisaki et al¹¹.

Figure 1: Schematic representations of culture dish surfaces treated with type I collagen. Under acidic conditions, type I collagen molecules are adsorbed on the surface of a dish in the non-fibrous form (left panel). Under neutral conditions at 37 °C, type I collagen molecules are reassembled into fibrils and adsorbed on the surface of dishes in the gel form (right panel). Please click here to view a larger version of this figure.

Figure 2: Morphology of FEPE1L-8 cells. FEPE1L-8 cells in K110 were cultured using the non-fibrous form (10 µg/mL; left panels) or fibril form (1 mg/mL; right panels) of type I collagen for 2 h (upper panels) or 3 days (lower panels). White bars indicate 100 µm. Figure 2 has been modified from Fujisaki et al. in Figure 1E–H¹¹. Please click here to view a larger version of this figure.

Figure 3: Proliferation of FEPE1L-8 cell. The number of viable cells were estimated on the non-fibrous form (black solid line, black filled circles) or on the fibril form (dotted line, open circle) of type I collagen, or untreated dish surfaces (gray dotted line, gray filled circles) for 2 h, 1 day, and 3 days. Experiments were performed in triplicates and values are shown as means + SD. This figure has been modified from Fujisaki et al. in Figure 1J¹¹. Please click here to view a larger version of this figure.

Discussion

Some ECM components, including type I collagen, form three-dimensional structures in vivo¹. Culturing on such a three-dimensional, gel substrate provides more physiological conditions in vitro than on a two-dimensional, plastic surface¹^,²^,³^,⁴. Numerous protocols regarding the gel culture method have been reported, such as using type I collagen¹^,²^,³^,⁴^,⁶^,⁷^,¹¹, type IV collagen¹⁴^,¹⁵, and Matrigel¹⁶. Type I collagen is a well-defined and widely used material because of its abundance and ease of handling. The features of purified type I collagen depend on the animal species, age, and purification methods⁵^,¹⁷. Type I collagen can be purified using acetic acid and/or proteases, such as pepsin, papain, and proctase⁵^,¹⁷. Acid-soluble collagen maintains amino-telopeptides and protease-soluble collagen are cleaved amino-telopeptides⁵^,¹⁷. The reserved length of amino-telopeptides depends on the type of proteases, and the presence of telopeptides affects fibril morphology and gel strength⁵^,¹⁷. The viscosity of acid-soluble collagen fibrils is greater than that of protease-treated collagens¹⁷. In this study, we used acid-soluble bovine type I collagen. Pepsin-solubilized collagen can also be used in this gel culture protocol; however, the gel strength is weaker¹⁷. These differences in materials can cause cell behavioral differences, but they are currently not well understood.

The gel culture protocol described in this study is very simple. Many modifications of this method have been reported. One possible modification for the culture of keratinocytes is to mimic the basement membrane. Type IV collagen gels may be better to keep a basement membrane-like substrate structure in vitro¹⁵^,¹⁸. However, a long incubation period is required for the preparation of type IV collagen gels¹⁴^,¹⁵^,¹⁸. Instead, mixing type IV collagen with type I collagen gels can produce novel culture substrates (type I/type IV collagen hybrid gels)¹⁹. These hybrid gels are easy to handle, require a short time for gelation, and yield more basement membrane-like conditions for keratinocytes. On type I/type IV collagen hybrid gels, keratinocytes survive, form colonies, and induce terminal differentiation¹⁹. This hybrid method has versatile applications.

On-gel culture using type I collagen affects cancer cells. On the fibril form of type I collagen, Akt activation and growth of Caco-2 cells (a colon cancer cell line) are suppressed⁷. In addition, the growth of human melanoma cells (M24met) on the fibril form is arrested at the G1/S checkpoint²⁰. Moreover, markedly increased levels of reactive oxygen species are observed in murine 3T3-L1 preadipocytes cultured on the fibril form. Furthermore, cell proliferation and migration are stimulated in opposite directions by the non-fibrous and fibril forms of type I collagen²¹.

Divulgaciones

The authors have nothing to disclose.

Acknowledgements

We are grateful to Dr. K. Sekiguchi (Institute for Protein Research, Osaka University), Dr. M. Yamada (Institute for Protein Research, Osaka University), Dr. T. Ikejima (China-Japan Research Institute of Medical and Pharmaceutical Sciences, Wuya College of Innovation, Shenyang Pharmaceutical University) and T. Hayashi (China-Japan Research Institute of Medical and Pharmaceutical Sciences, Wuya College of Innovation, Shenyang Pharmaceutical University) for helpful comments.

Materials

Albumin, from bovine serum (BSA)	Merck KGaA	A4503
1 % BSA	Merck KGaA	A4503	Dissolve 1 g of BSA powder in 100 mL of PBS (-) and filtrate
Cell Counting Kit-8	Dojindo Molecular Technologies, Inc.	347-07621	tetrazolium salt, 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H tetrazolium, monosodium salt (WST-8)
Collagen type I (Acid soluble collgen)	Nippi Inc.	ASC-1-100-20	from bovine (any other species available, concentration is 3.0 mg/mL
disposable membrane filter unit DISMIC cellulose acetate	ADVANTEC Co., LTD.	25CS020AS	0.2 µm pore size
human keratinocyte line cell FEPE1L-8			Donated Dr.W.G. Carter (Fred Hutchinson Cancer Research Center, Seattle, WA)
K-1	Kyokuto Seiyaku Inc.	28204	additive supplement with 500 mg of BSA, 500 mg of bovine pituitarybody extracts, 2.5 mg of insulin, 0.05 µg of h-EGF and 5 mg of heparin
K110 Type-II medium	Kyokuto Seiyaku Inc.	28204	keratinocyte basal culture medium
K110 Type-II medium with K-1 and Penicillin-Streptomycin (K110)	Kyokuto Seiyaku Inc.	28204	Add 5 mL of Penicillin-Streptomycin and 10 mL of additive supplement (K-1) in 500 mL of K110 type-II keratinocyte basal culture medium
PBS (-)	Merck KGaA	P-5368	Dissolve 1 pouch of PBS (-) powder in 1000 mL of deionized water and filtrate
10x PBS (-)	Merck KGaA	P-5368	Dissolve 1 pouch of PBS (-) powder in 100 mL of deionized water and filtrate
Penicillin-Streptomycin	MP Biomedicals, LLC	1670049	10000 units/mL of penisillin G and 10,000μg/mL of streptmycin sulfate in physiological saline
Phosphate bufferred saline BioPerformance CertiCertified, pH 7.4	Merck KGaA	P-5368-10 pack
Trypsin from porcine pancreas	Merck KGaA	T4799
0.05 % trypsin	Merck KGaA	T4799	Dissolve 0.25 g of trypsin and 0.186 g of EDTA.2Na in 500 mL of PBS (-) and filtrate
Trypsin inhibitor from soybean	FUJIFILM Wako Pure Chemical corporation	202-20123
Trypsin inhibitor	FUJIFILM Wako Pure Chemical corporation	202-20123	Dissolve 50 mg of trypsin inhibitor and 500 mg of BSA in 500 mL of PBS (-) and filtrate

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Fujisaki, H., Futaki, S., Mizuno, K., Hattori, S. Evaluation of Keratinocyte Proliferation on Two- and Three-dimensional Type I Collagen Substrates. J. Vis. Exp. (146), e59339, doi:10.3791/59339 (2019).