Division of Molecular Medicine, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Torrance, California 90502, USA.
Invest Ophthalmol Vis Sci. 2010 Jun;51(6):2943-8. doi: 10.1167/iovs.09-4639. Epub 2010 Jan 20.
Epidermal growth factor (EGF) stimulates migration in corneal epithelial wound healing. The purpose of this study was to investigate the effect of EGF-induced alpha-tubulin deacetylation through activating HDAC6 on migration in corneal epithelial wound healing.
Human corneal epithelial (HCE) cells were cultured in DMEM/F12 medium containing 10% FBS in a 37 degrees C incubator supplied with 5% CO(2). Western blot analysis was used to determine protein expression. Activity of HDAC6 was suppressed by trichostatin A (TSA) and by siRNA specific to HDAC6. Corneal epithelial cell migration was measured by using scratch-induced directional migration assay in cultured cells and by corneal epithelial debridement using a mouse whole-eye organ culture model.
The authors found EGF stimulated corneal epithelial cell migration in wound healing by enhancing HDAC6 activity, resulting in the deacetylation of alpha-tubulin. EGF stimulated HDAC6 enzymatic activity and protein translocation toward the leading edge of the cell. Inhibition of HDAC6 activity by TSA significantly suppressed EGF-induced cell migration and delayed EGF-induced wound healing in epithelially debrided mouse corneas. In the meantime, knockdown of HDAC6 mRNA with specific siRNA effectively abolished EGF-induced deacetylation of alpha-tubulin, resulting in the inhibition of cell migration.
These results reveal an important mechanism that involves EGF-induced HDAC6 activation and alpha-tubulin deacetylation, subsequently affecting corneal epithelial migration in the wound-healing process.
表皮生长因子(EGF)可刺激角膜上皮伤口愈合中的迁移。本研究旨在探讨 EGF 通过激活 HDAC6 诱导α-微管蛋白去乙酰化对角膜上皮伤口愈合中迁移的影响。
人角膜上皮(HCE)细胞在含有 10%FBS 的 DMEM/F12 培养基中于 37℃、5%CO2 培养箱中培养。采用 Western blot 分析检测蛋白表达。用曲古抑菌素 A(TSA)和 HDAC6 特异性 siRNA 抑制 HDAC6 活性。采用划痕诱导的定向迁移测定法在培养细胞中测量角膜上皮细胞迁移,并用小鼠全眼器官培养模型进行角膜上皮清创术。
作者发现 EGF 通过增强 HDAC6 活性刺激角膜上皮细胞迁移,从而导致α-微管蛋白去乙酰化,从而促进伤口愈合中的细胞迁移。EGF 刺激 HDAC6 酶活性并将其蛋白转位到细胞前缘。TSA 抑制 HDAC6 活性可显著抑制 EGF 诱导的细胞迁移,并延迟上皮清创的小鼠角膜中 EGF 诱导的伤口愈合。同时,用特异性 siRNA 敲低 HDAC6 mRNA 可有效消除 EGF 诱导的α-微管蛋白去乙酰化,从而抑制细胞迁移。
这些结果揭示了一个重要的机制,即 EGF 诱导的 HDAC6 激活和α-微管蛋白去乙酰化,随后影响伤口愈合过程中的角膜上皮迁移。