Summary

RNA-interferentie op basis van onderzoek naar de functie van heat shock protein 27 tijdens cornea epitheliale wondheling

Published: September 27, 2016
doi:

Summary

Herein, we present a protocol to use heat shock protein 27 (HSP27)-specific small interfering RNA to assess the function of HSP27 during corneal epithelial wound healing. RNA interference is the best method for effectively knocking-down gene expression to investigate protein function in various cell types.

Abstract

Small interfering RNA (siRNA) is among the most widely used RNA interference methods for the short-term silencing of protein-coding genes. siRNA is a synthetic RNA duplex created to specifically target a mRNA transcript to induce its degradation and it has been used to identify novel pathways in various cellular processes. Few reports exist regarding the role of phosphorylated heat shock protein 27 (HSP27) in corneal epithelial wound healing. Herein, cultured human corneal epithelial cells were divided into a scrambled control-siRNA transfected group and a HSP27-specific siRNA-transfected group. Scratch-induced directional wounding assays, and western blotting, and flow cytometry were then performed. We conclude that HSP27 has roles in corneal epithelial wound healing that may involve epithelial cell apoptosis and migration. Here, step-by-step descriptions of sample preparation and the study protocol are provided.

Introduction

Corneale epitheliale cellen (LME) continu afgestoten in traanfilm, terwijl ze tegelijkertijd vervangen door cellen van de limbus en corneale epitheliale basale lagen. 1 verschillende extrinsieke stressoren kunnen de apoptose en afschilfering van CECs induceren. 2 De heat shock eiwitten (HSP) zijn sterk geconserveerd en kunnen worden onderverdeeld in twee families op basis van molecuulgrootte. 3 de grootste HSP-familie omvat HSP90, HSP70 en HSP60 en de kleine familie omvat HSP27. 4 de fosforylatie van HSP27 speelt een belangrijke rol in celoverleving spelen en is vereist voor celmigratie vanwege de rol van dit eiwit in actine remodellering. 5-7 Daarom hebben we geprobeerd om de mogelijke rol van HSP27 fosforylatie in CEC migratie en apoptose getest in een in vitro model van epitheliale wondgenezing.

RNA-interferentie (RNAi) met behulp van kleine of korte interfererende RNA (siRNA) heeft generated belangstelling voor zowel fundamenteel als toegepast biologie, omdat het mogelijk maakt de expressie van elk gen van belang worden overreden. 8 Hierin gebruikten we HSP27-specifiek siRNA om de bijdrage van HSP27 CEC wondgenezing en apoptose beoordelen. Traditionele werkwijzen voor RNAi gen knock-in cellen gebruiken synthetische RNA duplexen, waaronder twee niet-gemodificeerd 21-meer oligonucleotiden die kunnen worden samengesteld om siRNA's te maken. De RNAi siRNA dat we in deze studie is een eenvoudige en efficiënte methode om cellen te transfecteren, en dit reagens werkt met verschillende geïmmortaliseerde cellijnen. In deze studie tonen we de voor deze analyse methoden, met inbegrip van een scratch-geïnduceerde directionele wond assay, western blotting, siRNA transfectie assay, immunofluorescentietest, en flowcytometrie.

Protocol

1. Cell Line Cultuur 10 6-telomerase geïmmortaliseerde humane corneale epitheelcellen (HCECs) in een 6-puts plaat (dichtheid: 1039,9 cellen / mm 2) in een 37 ° C incubator met 5% CO2 atmosfeer via luchtwegepitheel groeimedium (BEGM) tot bereiken ze 95% samenvloeiing. 2. Western Blot Analyse Na het aanmaken van Epitheliale Scratch Wonden Streak een steriele 200 ul pipetpunt over het oppervlak van een putje van confluente cultuur H…

Representative Results

De expressie van HSP27 gefosforyleerde significant verhoogd 5, 10 en 30 minuten na kras verwonding vergeleken met verwonde HCECs 13. Western blot analyse toonde dat de expressie van HSP27 en gefosforyleerde Akt gefosforyleerd waren beide aanzienlijk verminderd, terwijl de expressie van Bax aanzienlijk HSP27-specifieke siRNA getransfecteerde HCECs (Figuur 1A-E) verhoogd. De gefosforyleerd HSP27 expressie werd verminderd met 30% en 40% in 10 nm en 50 nm van HSP2…

Discussion

In this present study, we evaluated the potential role of HSP27 in corneal epithelial wounding using in vitro approaches. The critical steps involved siRNA transfection for HSP27 knock-down to observe the function of HSP27 in cells subjected to stress. Notably, a role for HSP27 was revealed by these experiments in epithelial cell migration and apoptosis during corneal epithelial wound healing. Unlike previous studies10 that used rat HSP27-specific siRNA to transfect vascular smooth muscle cells, we us…

Disclosures

The authors have nothing to disclose.

Acknowledgements

Deze studie werd ondersteund door de Student Research Grant (13-14) van de Universiteit van Ulsan College of Medicine, Seoul, Korea en een subsidie ​​(2014-464) van de Asan Institute for Life Sciences, Seoul, Korea.

Materials

Biological safety cabinet CHC LAB Co.Ltd,  Daejeon, Republic of Korea  CHC-777A2-06 Class II, Type A2 
Stealth RNAi™ siRNA Thermo Fisher Scientific, Inc., Waltham, MA RNAi siRNA; scrambled control-siRNA and HSP27-specific siRNA
BEGMTM Lonza, Inc., Walkersville, MD CC-3171, CC4175 Bronchial epithelium growth medium 
Protease inhibitor  Sigma-Aldrich, Inc., St. Louis, MO P8340 ,P7626 1 uM Pepstatin A, 1 uM Leupetin, 0.1 uM Aprotin
Bradford protein assay  Bio-Rad Laboratories, Hercules, CA #500-0001 Bradford protein assay 
Nitrocellulose filters  Amersham, Little Chalfont, UK RPN3032D Western blotting membrane
Non-phosphorylated HSP27  Abcam Inc., Cambridge, MA ab12351 1:1000 dilution (Total HSP27)
Phosphorylated HSP27 (Ser85) Abcam Inc., Cambridge, MA ab5594 1: 1000 dilution HSP27 was phosphorylated at Ser85
Lipofectamine® RNAiMAX reagent  Invitrogen, Carlsbad, CA 13-778-075 Transfection reagent
Phosphorylated Akt (Ser473) Cell Signaling Technology, Danvers, MA No. 4060 1: 1000 dilution Akt was phosphorylated at Ser473 (cell survival marker)
Non-phosphorylated Akt  Cell Signaling Technology, Danvers, MA No. 4061 1:1000 dilution (Total Akt)
Bcl-2-associated X protein  Cell Signaling Technology, Danvers, MA No. 4062 1: 1000 (anti-apoptotic protein marker)
GAPDH Santa Cruz Biotechnology, Santa Cruz, CA No. 4063 1:1000 loading control  marker (house keeping gene)
Horseradish peroxidase-conjugated goat anti-rabbit antibodies Thermo Fisher Scientific, Inc., Waltham, MA NCI1460KR 1:10000 dilution
OPTI-MEM Invitrogen, Carlsbad, CA 31985 reduced serum medium for transfection
Image analysis software Olympus, Inc., Tokyo, Japan Image-Pro Plus 5.0
Skimed milk powder  Carl Roth GmbH + Co. KG, Karlstruhe, Germany T145.2
Tris  Amresco LCC, Inc. Solon, OH No-0497
Sodium Chloride  Amresco LCC, Inc. Solon, OH No-0241
Six well culture plate Thermo Fisher Scientific, Inc., Waltham, MA 140675 35.00 mm diameter / well
24-well culuture dish Thermo Fisher Scientific, Inc., Waltham, MA 142475
Orbital shaker N-Bioteck, Inc., Seoul, South Korea NB1015
Bovine serum albumin Santa Cruz Biotechnology, Santa Cruz, CA sc-2323 
BDFACSCantoTM II BD Biosciences, Franklin Lakes, NJ Flow cytometry
X-Ray Film Kodak, Rochester, NY Medical X-Ray Cassette with Green 400 Screen 
western blotting luminol reagent Santa Cruz Biotechnology, Santa Cruz, CA sc-2048 
FITC Annexin V Apoptosis Detection Kit I BD Biosciences, Franklin Lakes, NJ 556547

References

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Cite This Article
Yoo, A., Park, H., Kang, S., Kim, E., Tchah, H., Kim, J. Y. RNA Interference-based Investigation of the Function of Heat Shock Protein 27 during Corneal Epithelial Wound Healing. J. Vis. Exp. (115), e54280, doi:10.3791/54280 (2016).

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