衰老大血管和微血管内皮细胞的表型改变

Ugo Cavallaro , Vera Castelli , Ugo Del Monte , Marco R. Soria
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引用次数: 30

摘要

内皮细胞衰老可能在与年龄相关的血管疾病中起关键作用。内皮细胞的体外和体内衰老之间存在密切的关系。因此,阐明内皮细胞在长期培养过程中发生的结构和功能变化将有助于阐明老年人血管疾病的发病机制。我们研究了复制性衰老对牛主动脉内皮细胞和微血管内皮细胞结构的影响。在两种细胞类型中均观察到细胞面积的显著增加,而仅在微血管内皮细胞中检测到显著的形态学改变。后者也显示肌动蛋白细胞骨架的年龄相关重组。最后,随着年龄的增长,主动脉内皮细胞和微血管内皮细胞都失去了对碱性成纤维细胞生长因子的迁移反应。我们的研究结果突出了衰老内皮细胞的结构和功能变化。这种重排可能解释了体内内皮细胞的改变与年龄相关的血管功能障碍有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenotypic Alterations in Senescent Large-Vessel and Microvascular Endothelial Cells

Endothelial cell senescence likely plays a key role in age-associated vascular diseases. A close relationship between in vitro and in vivo senescence of endothelial cells has been established. Therefore, elucidating the structural and functional changes occurring during long-term cultures of endothelial cells would contribute to clarifying the pathogenesis of vascular disorders in the elderly. We investigated the effects of replicative senescence on the architecture of bovine aortic vs microvascular endothelial cells. A marked increase in cell area was observed in both cell types, whereas dramatic morphological alterations were detected in microvascular endothelial cells only. The latter also showed age-associated reorganization of the actin cytoskeleton. Finally, both aortic and microvascular endothelial cells lost their migratory response to basic fibroblast growth factor with age. Our results highlight dramatic structural and functional alterations in senescent endothelial cells. Such rearrangements might account for in vivo endothelial cell alterations involved in age-associated vascular dysfunction.

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