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骨髓来源的祖细胞对血管和心脏再生的贡献。

Contribution of marrow-derived progenitors to vascular and cardiac regeneration.

作者信息

Rafii Shahin, Meeus Sarah, Dias Sergio, Hattori Koichi, Heissig Beate, Shmelkov Sergey, Rafii Daniel, Lyden David

机构信息

Cornell University Medical College, New York, USA.

出版信息

Semin Cell Dev Biol. 2002 Feb;13(1):61-7. doi: 10.1006/scdb.2001.0285.

Abstract

Adult bone marrow is a rich reservoir of tissue-specific pluripotent stem and progenitor cells. Accumulating evidence suggest that these cells have the potential of contributing to tissue revascularization and cardiac regeneration. Physiological stress results in the release of specific chemokines and cytokines that promote mobilization of stem cells to the peripheral circulation. Incorporation of these mobilized cells contributes to formation of functional vasculature and sets up stage for tissue regeneration. Vascular Endothelial Growth Factor (VEGF) through interaction with its receptors VEGFR2 and VEGFR1 expressed on endothelial and hematopoietic stem cells promote recruitment of these cells into the sites of tissue injury accelerating vascular healing. Similarly, subset of CD34 + marrow derived cells are mobilized and recruited to the ischemic myocardium, differentiating into cardiac and vascular cells, restoring cardiac function. Identification of cellular mediators and tissue specific chemocytokines that facilitate selective recruitment of marrow-derived stem and progenitor cells to specific organs, will open up new avenues to accelerate cardiovascular regeneration and tissue revascularization.

摘要

成人骨髓是组织特异性多能干细胞和祖细胞的丰富储存库。越来越多的证据表明,这些细胞具有促进组织血管再生和心脏再生的潜力。生理应激会导致特定趋化因子和细胞因子的释放,从而促进干细胞向外周循环的动员。这些动员细胞的掺入有助于功能性脉管系统的形成,并为组织再生奠定基础。血管内皮生长因子(VEGF)通过与其在内皮细胞和造血干细胞上表达的受体VEGFR2和VEGFR1相互作用,促进这些细胞募集到组织损伤部位,加速血管愈合。同样,CD34 + 骨髓来源细胞的亚群被动员并募集到缺血心肌,分化为心脏和血管细胞,恢复心脏功能。鉴定促进骨髓来源的干细胞和祖细胞选择性募集到特定器官的细胞介质和组织特异性趋化因子,将为加速心血管再生和组织血管再生开辟新途径。

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