Stem Cell Institute, James Brown Cancer Center, Department of Ophthalmology and Visual Sciences, University of Louisville School of Medicine, 301 E. Muhammad Ali Blvd., Louisville, KY 40202, USA.
Biochem Biophys Res Commun. 2010 Feb 19;392(4):593-8. doi: 10.1016/j.bbrc.2010.01.084. Epub 2010 Jan 25.
14-3-3sigma (also called stratifin) is specifically expressed in the stratified squamous epithelium and its function was recently shown to be linked to epidermal stratification and differentiation in the skin. In this study, we investigated its role in corneal epithelium cell proliferation and differentiation. We showed that the 14-3-3sigma mutation in repeated epilation (Er) mutant mice results in a dominant negative truncated protein. Primary corneal epithelial cells expressing the dominant negative protein failed to undergo high calcium-induced cell cycle arrest and differentiation. We further demonstrated that blocking endogenous 14-3-3sigma activity in corneal epithelial cells by overexpressing dominative negative 14-3-3sigma led to reduced Notch activity and Notch1/2 transcription. Significantly, expression of the active Notch intracellular domain overcame the block in epithelial cell differentiation in 14-3-3sigma mutant-expressing corneal epithelial cells. We conclude that 14-3-3sigma is critical for regulating corneal epithelial proliferation and differentiation by regulating Notch signaling activity.
14-3-3sigma(也称为 stratifin)特异性表达于复层鳞状上皮,其功能最近被证明与皮肤的表皮分层和分化有关。在这项研究中,我们研究了其在角膜上皮细胞增殖和分化中的作用。我们表明,复发性脱毛(Er)突变小鼠中的 14-3-3sigma 突变导致显性负截断蛋白。表达显性负蛋白的原代角膜上皮细胞无法经历高钙诱导的细胞周期停滞和分化。我们进一步证明,通过过表达显性负 14-3-3sigma 阻断角膜上皮细胞内源性 14-3-3sigma 的活性导致 Notch 活性和 Notch1/2 转录降低。重要的是,表达活性 Notch 细胞内结构域克服了在表达 14-3-3sigma 的角膜上皮细胞中上皮细胞分化的阻断。我们的结论是,14-3-3sigma 通过调节 Notch 信号活性对于调节角膜上皮细胞的增殖和分化至关重要。