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干细胞鲜为人知的一面:干细胞中的小窝蛋白-1与小窝,组织修复与再生

The less-often-traveled surface of stem cells: caveolin-1 and caveolae in stem cells, tissue repair and regeneration.

作者信息

Baker Natasha, Tuan Rocky S

出版信息

Stem Cell Res Ther. 2013 Jul 30;4(4):90. doi: 10.1186/scrt276.

Abstract

Stem cells are an important resource for tissue repair and regeneration. While a great deal of attention has focused on derivation and molecular regulation of stem cells, relatively little research has focused on how the subcellular structure and composition of the cell membrane influences stem cell activities such as proliferation, differentiation and homing. Caveolae are specialized membrane lipid rafts coated with caveolin scaffolding proteins, which can regulate cholesterol transport and the activity of cell signaling receptors and their downstream effectors. Caveolin-1 is involved in the regulation of many cellular processes, including growth, control of mitochondrial antioxidant levels, migration and senescence. These activities are of relevance to stem cell biology, and in this review evidence for caveolin-1 involvement in stem cell biology is summarized. Altered stem and progenitor cell populations in caveolin-1 null mice suggest that caveolin-1 can regulate stem cell proliferation, and in vitro studies with isolated stem cells suggest that caveolin-1 regulates stem cell differentiation. The available evidence leads us to hypothesize that caveolin-1 expression may stabilize the differentiated and undifferentiated stem cell phenotype, and transient downregulation of caveolin-1 expression may be required for transition between the two. Such regulation would probably be critical in regenerative applications of adult stem cells and during tissue regeneration. We also review here the temporal changes in caveolin-1 expression reported during tissue repair. Delayed muscle regeneration in transgenic mice overexpressing caveolin-1 as well as compromised cardiac, brain and liver tissue repair and delayed wound healing in caveolin-1 null mice suggest that caveolin-1 plays an important role in tissue repair, but that this role may be negative or positive depending on the tissue type and the nature of the repair process. Finally, we also discuss how caveolin-1 quiescence-inducing activities and effects on mitochondrial antioxidant levels may influence stem cell aging.

摘要

干细胞是组织修复和再生的重要资源。尽管大量关注集中在干细胞的衍生和分子调控上,但相对较少的研究聚焦于细胞膜的亚细胞结构和组成如何影响干细胞的活动,如增殖、分化和归巢。小窝是由小窝蛋白支架蛋白包被的特殊膜脂筏,其可调节胆固醇转运以及细胞信号受体及其下游效应器的活性。小窝蛋白-1参与许多细胞过程的调控,包括生长、线粒体抗氧化水平的控制、迁移和衰老。这些活动与干细胞生物学相关,在本综述中,总结了小窝蛋白-1参与干细胞生物学的证据。小窝蛋白-1基因敲除小鼠中干细胞和祖细胞群体的改变表明小窝蛋白-1可调节干细胞增殖,而对分离的干细胞进行的体外研究表明小窝蛋白-1可调节干细胞分化。现有证据使我们推测小窝蛋白-1的表达可能稳定分化和未分化的干细胞表型,而两者之间的转变可能需要小窝蛋白-1表达的短暂下调。这种调控在成体干细胞的再生应用以及组织再生过程中可能至关重要。我们还在此综述了组织修复过程中报道的小窝蛋白-1表达的时间变化。过表达小窝蛋白-1的转基因小鼠中肌肉再生延迟,以及小窝蛋白-1基因敲除小鼠中心脏、大脑和肝脏组织修复受损以及伤口愈合延迟,表明小窝蛋白-1在组织修复中起重要作用,但该作用可能因组织类型和修复过程的性质而呈负性或正性。最后,我们还讨论了小窝蛋白-1的诱导静止活性以及对线粒体抗氧化水平的影响如何可能影响干细胞衰老。

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