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细胞外基质与细胞形状:抑制血管生成的潜在控制点。

Extracellular matrix and cell shape: potential control points for inhibition of angiogenesis.

作者信息

Ingber D

机构信息

Surgical Research Laboratory, Children's Hospital, Boston, MA 02115.

出版信息

J Cell Biochem. 1991 Nov;47(3):236-41. doi: 10.1002/jcb.240470309.

Abstract

Capillary endothelial (CE) cells require two extracellular signals in order to switch from quiescence to growth and back to differentiation during angiogenesis: soluble angiogenic factors and insoluble extracellular matrix (ECM) molecules. Soluble endothelial mitogens, such as basic fibroblast growth factor (FGF), act over large distances to trigger capillary growth, whereas ECM molecules act locally to modulate cell responsiveness to these soluble cues. Recent studies reveal that ECM molecules regulate CE cell growth and differentiation by modulating cell shape and by activating intracellular chemical signaling pathways inside the cell. Recognition of the importance of ECM and cell shape during capillary morphogenesis has led to the identification of a series of new angiogenesis inhibitors. Elucidation of the molecular mechanism of capillary regulation may result in development of even more potent angiogenesis modulators in the future.

摘要

在血管生成过程中,毛细血管内皮(CE)细胞需要两种细胞外信号才能从静止状态转变为生长状态,然后再回到分化状态:可溶性血管生成因子和不溶性细胞外基质(ECM)分子。可溶性内皮细胞有丝分裂原,如碱性成纤维细胞生长因子(FGF),可在远距离发挥作用以触发毛细血管生长,而ECM分子则在局部发挥作用,调节细胞对这些可溶性信号的反应。最近的研究表明,ECM分子通过调节细胞形状和激活细胞内的化学信号通路来调节CE细胞的生长和分化。认识到ECM和细胞形状在毛细血管形态发生过程中的重要性,已导致一系列新的血管生成抑制剂的鉴定。阐明毛细血管调节的分子机制可能会在未来开发出更有效的血管生成调节剂。

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