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体外基底膜诱导血管分化所涉及的细胞内机制。

Intracellular mechanisms involved in basement membrane induced blood vessel differentiation in vitro.

作者信息

Grant D S, Lelkes P I, Fukuda K, Kleinman H K

机构信息

Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, NIH, Bethesda, Maryland 20892.

出版信息

In Vitro Cell Dev Biol. 1991 Apr;27A(4):327-36. doi: 10.1007/BF02630910.

Abstract

The extracellular matrix, particularly basement membranes, plays an important role in angiogenesis (blood vessel formation). Previous work has demonstrated that a basement membranelike substrate (Matrigel) induces human umbilical vein endothelial cells to rapidly form vessel-like tubes (Kubota, et al., 1988; Grant et al., 1989b); however, the precise mechanism of tube formation is unclear. Using this in vitro model, we have investigated morphologic changes occurring during tube formation and the cytoskeletal and protein synthesis requirements of this process. Electron microscopy showed that endothelial cells attach to the Matrigel surface, align, and form cylindrical structures that contain a lumen and polarized cytoplasmic organelles. The cytoskeleton is reorganized into bundles of actin filaments oriented along the axis of the tubes and is located at the periphery of the cells. The addition of colchicine or cytochalasin D blocked tube formation, indicating that both microfilaments and microtubules are involved in this process. Cycloheximide blocked tube formation by 100%, indicating that the process also required protein synthesis. In particular, collagen synthesis seems to be required for tube formation because cis-hydroxyproline inhibited tube formation, whereas either the presence of ascorbic acid or the addition of exogenous collagen IV to the Matrigel increased tube formation. Our results indicate that endothelial cell attachment to Matrigel induces the reorganization of the cytoskeleton and elicits the synthesis of specific proteins required for the differentiated phenotype of the cells.

摘要

细胞外基质,尤其是基底膜,在血管生成(血管形成)中起着重要作用。先前的研究表明,一种类似基底膜的基质(基质胶)可诱导人脐静脉内皮细胞迅速形成血管样管腔(久保田等人,1988年;格兰特等人,1989年b);然而,管腔形成的确切机制尚不清楚。利用这种体外模型,我们研究了管腔形成过程中发生的形态变化以及该过程对细胞骨架和蛋白质合成的需求。电子显微镜显示,内皮细胞附着于基质胶表面,排列并形成含有管腔和极化细胞质细胞器的圆柱形结构。细胞骨架重新组织成沿管腔轴排列的肌动蛋白丝束,并位于细胞周边。秋水仙碱或细胞松弛素D的添加会阻止管腔形成,表明微丝和微管均参与此过程。放线菌酮可100%阻止管腔形成,表明该过程也需要蛋白质合成。特别是,管腔形成似乎需要胶原蛋白合成,因为顺式羟脯氨酸会抑制管腔形成,而抗坏血酸的存在或向基质胶中添加外源性胶原蛋白IV则会增加管腔形成。我们 的结果表明,内皮细胞与基质胶的附着会诱导细胞骨架的重组,并引发细胞分化表型所需的特定蛋白质的合成。

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