Summary

Indagine basata RNA interferenza della funzione di shock termico proteine ​​27 durante la guarigione della ferita corneale epiteliale

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

Corneali cellule epiteliali (PEC) sono continuamente capannone in film lacrimale, mentre sono allo stesso tempo sostituite da cellule del limbus e corneali strati basali epiteliali. 1 vari fattori di stress estrinseci possono indurre l'apoptosi e desquamazione della CEC. 2 Le proteine da shock termico (HSP) sono altamente conservati e possono essere suddivisi in due famiglie secondo dimensione molecolare. 3 la più grande famiglia HSP comprende HSP90, HSP70 e HSP60, e la famiglia più piccola comprende HSP27. 4 la fosforilazione di HSP27 è noto a svolgere un ruolo importante nella sopravvivenza cellulare ed è necessario per la migrazione delle cellule a causa del ruolo di questa proteina in actina rimodellamento. 5-7 Pertanto, abbiamo cercato di verificare il ruolo potenziale di HSP27 fosforilazione nella migrazione CEC e l'apoptosi in un modello in vitro di cellule epiteliali guarigione della ferita.

RNA interference (RNAi) utilizzando sia piccoli o brevi RNA interferenti (siRNA) ha geinteressi nerated sia in biologia di base e applicata, in quanto consente potenzialmente l'espressione di un gene di interesse da abbattuto. 8 In questo, abbiamo usato specifici siRNA-HSP27 per valutare il contributo di HSP27 a CEC guarigione della ferita e l'apoptosi. i metodi tradizionali per RNAi gene knock-down in cellule utilizzano duplex RNA sintetici, tra cui due non modificati oligonucleotidi 21-mer che possono essere assemblati per creare siRNA. La RNAi siRNA che abbiamo usato in questo studio è un metodo semplice e molto efficace trasfezione le cellule, e questo reagente funziona con varie linee cellulari immortalizzate. In questo studio, abbiamo dimostrato i metodi utilizzati per questa analisi, tra cui un saggio di zero-indotta ferita direzionale, western blotting, saggio di transfezione siRNA, test di immunofluorescenza e citometria a flusso.

Protocol

1. Cell Line Culture 10 6 umani corneali cellule epiteliali telomerasi-immortalata (HCECs) in un 6-pozzetti (densità: 1039,9 cellule / mm 2) in un incubatore a 37 ° con un'atmosfera 5% di CO 2 con terreno di crescita dell'epitelio bronchiale (BEGM) fino raggiungono il 95% di confluenza. 2. Analisi Western Blot dopo aver creato epiteliali Ferite Scratch Streak uno sterile 200 ml punta della pipetta sulla superficie di un p…

Representative Results

L'espressione di HSP27 fosforilata significativamente aumentata a 5, 10, e 30 minuti dopo il ferimento zero confrontato con HCECs illesi 13. Analisi Western Blot ha rivelato che l'espressione di HSP27 fosforilata e fosforilata Akt sono stati entrambi significativamente ridotto, mentre l'espressione di Bax era significativamente aumentata in HCECs siRNA-trasfettate specifici Hsp27 (Figura 1A-E). L'espressione HSP27 fosforilata è stato ridotto d…

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

Questo studio è stato sostenuto dalla Student Research Grant (13-14) dell'Università di Ulsan College of Medicine, Seoul, Corea e una borsa di studio (2014-464) presso l'Istituto di Scienze della Vita Asan, Seoul, Corea.

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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