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肌动蛋白丝组织调节晶状体细胞分化和存活的诱导。

Actin filament organization regulates the induction of lens cell differentiation and survival.

作者信息

Weber Gregory F, Menko A Sue

机构信息

Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, 571 Jefferson Alumni Hall, 1020 Locust Street, Philadelphia, PA 19107, USA.

出版信息

Dev Biol. 2006 Jul 15;295(2):714-29. doi: 10.1016/j.ydbio.2006.03.056. Epub 2006 Apr 7.

Abstract

The actin cytoskeleton has the unique capability of integrating signaling and structural elements to regulate cell function. We have examined the ability of actin stress fiber disassembly to induce lens cell differentiation and the role of actin filaments in promoting lens cell survival. Three-dimensional mapping of basal actin filaments in the intact lens revealed that stress fibers were disassembled just as lens epithelial cells initiated their differentiation in vivo. Experimental disassembly of actin stress fibers in cultured lens epithelial cells with either the ROCK inhibitor Y-27632, which destabilizes stress fibers, or the actin depolymerizing drug cytochalasin D induced expression of lens cell differentiation markers. Significantly, short-term disassembly of actin stress fibers in lens epithelial cells by cytochalasin D was sufficient to signal lens cell differentiation. As differentiation proceeds, lens fiber cells assemble actin into cortical filaments. Both the actin stress fibers in lens epithelial cells and the cortical actin filaments in lens fiber cells were found to be necessary for cell survival. Sustained cytochalasin D treatment of undifferentiated lens epithelial cells suppressed Bcl-2 expression and the cells ultimately succumbed to apoptotic cell death. Inhibition of Rac-dependent cortical actin organization induced apoptosis of differentiating lens fiber cells. Our results demonstrate that disassembly of actin stress fibers induced lens cell differentiation, and that actin filaments provide an essential survival signal to both lens epithelial cells and differentiating lens fiber cells.

摘要

肌动蛋白细胞骨架具有整合信号和结构元件以调节细胞功能的独特能力。我们研究了肌动蛋白应力纤维解聚诱导晶状体细胞分化的能力以及肌动蛋白丝在促进晶状体细胞存活中的作用。对完整晶状体中基底肌动蛋白丝的三维映射显示,就在晶状体上皮细胞在体内开始分化时,应力纤维发生了解聚。用ROCK抑制剂Y-27632(其使应力纤维不稳定)或肌动蛋白解聚药物细胞松弛素D在培养的晶状体上皮细胞中实验性地解聚肌动蛋白应力纤维,可诱导晶状体细胞分化标志物的表达。重要的是,细胞松弛素D对晶状体上皮细胞中肌动蛋白应力纤维的短期解聚足以引发晶状体细胞分化。随着分化的进行,晶状体纤维细胞将肌动蛋白组装成皮质丝。发现晶状体上皮细胞中的肌动蛋白应力纤维和晶状体纤维细胞中的皮质肌动蛋白丝对于细胞存活都是必需的。用细胞松弛素D持续处理未分化的晶状体上皮细胞会抑制Bcl-2表达,细胞最终死于凋亡性细胞死亡。抑制Rac依赖性皮质肌动蛋白组织会诱导分化的晶状体纤维细胞凋亡。我们的结果表明,肌动蛋白应力纤维的解聚诱导了晶状体细胞分化,并且肌动蛋白丝为晶状体上皮细胞和分化的晶状体纤维细胞提供了至关重要的存活信号。

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