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内皮祖细胞生物学的病理生理学和介入作用的当前观点:聚焦于 PI3K/AKT/eNOS 通路。

Current perspective of pathophysiological and interventional effects on endothelial progenitor cell biology: focus on PI3K/AKT/eNOS pathway.

机构信息

Laboratory of Cell Biology and Histology, University of Antwerp, Antwerp, Belgium.

出版信息

Int J Cardiol. 2010 Oct 29;144(3):350-66. doi: 10.1016/j.ijcard.2010.04.018. Epub 2010 May 4.

Abstract

For more than a decade, endothelial progenitor cells (EPCs) have been implicated in cardiovascular homeostasis. EPCs are believed to reside within the bone marrow in close contact with surrounding stromal cells, and, under stimulation of pro-inflammatory cytokines, EPCs are mobilized out of the bone marrow. Hereafter circulating EPCs home to peripheral tissues, undergoing further proliferation and differentiation. Under certain pathophysiologic conditions this process seems to be blunted, resulting in a reduced capacity of EPCs to engage in vasculogenesis at sites of endothelial injury or tissue ischemia. In this review, we focus on the effects of traditional cardiovascular risk factors on EPC biology and we explore whether pharmacological, dietary and lifestyle interventions can favorably restore EPC mobilization, differentiation, homing and angiogenic properties. Because the PI3K/Akt/eNOS pathway plays a pivotal role in the process of EPC mobilization, migration and homing, we specifically emphasize the involvement of PI3K, Akt and eNOS in EPC biology under these different (patho)physiologic conditions. (Pre)clinically used drugs or lifestyle interventions that have been shown to ameliorate EPC biology are reviewed. These treatment strategies remain attractive targets to restore the regenerative capacity of EPCs in cardiovascular diseases.

摘要

十多年来,内皮祖细胞 (EPCs) 一直被认为与心血管稳态有关。EPCs 被认为存在于骨髓中,与周围的基质细胞密切接触,在促炎细胞因子的刺激下,EPCs 从骨髓中动员出来。此后,循环 EPC 归巢到外周组织,进一步增殖和分化。在某些病理生理条件下,这个过程似乎受到了抑制,导致 EPC 参与内皮损伤或组织缺血部位血管生成的能力降低。在这篇综述中,我们重点关注传统心血管危险因素对 EPC 生物学的影响,并探讨了药物、饮食和生活方式干预是否可以有利地恢复 EPC 的动员、分化、归巢和血管生成特性。由于 PI3K/Akt/eNOS 途径在 EPC 动员、迁移和归巢过程中起着关键作用,我们特别强调了 PI3K、Akt 和 eNOS 在这些不同的(病理)生理条件下对 EPC 生物学的参与。我们回顾了已被证明能改善 EPC 生物学的(前)临床应用药物或生活方式干预。这些治疗策略仍然是恢复心血管疾病中 EPC 再生能力的有吸引力的目标。

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