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细胞间通讯的机制:细胞外膜囊泡的优缺点。

Extracellular membrane vesicles as a mechanism of cell-to-cell communication: advantages and disadvantages.

机构信息

Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche, University of Palermo, Palermo, Italy.

出版信息

Am J Physiol Cell Physiol. 2014 Apr 1;306(7):C621-33. doi: 10.1152/ajpcell.00228.2013. Epub 2014 Jan 22.

Abstract

Microvesicles represent a newly identified mechanism of intercellular communication. Two different types of microvesicles have been identified: membrane-derived vesicles (EVs) and exosomes. EVs originate by direct budding from the plasma membrane, while exosomes arise from ectocytosis of multivesicular bodies. Recent attention has focused on the capacity of EVs to alter the phenotype of neighboring cells to make them resemble EV-producing cells. Stem cells are an abundant source of EVs, and the interaction between stem cells and the microenvironment (i.e., stem cell niche) plays a critical role in determining stem cell phenotype. The stem cell niche hypothesis predicts that stem cell number is limited by the availability of niches releasing the necessary signals for self-renewal and survival, and the niche thus provides a mechanism for controlling and limiting stem cell numbers. EVs may play a fundamental role in this context by transferring genetic information between cells. EVs can transfer mRNA and microRNA to target cells, both of which may be involved in the change in target-cell phenotype towards that of EV-producing cells. The exchange of genetic information may be bidirectional, and EV-mediated transfer of genetic information after tissue damage may reprogram stem cells to acquire the phenotypic features of the injured tissue cells. In addition, stem cell-derived EVs may induce the de-differentiation of cells that survive injury by promoting their reentry into the cell cycle and subsequently increasing the possibility of tissue regeneration.

摘要

微泡代表了一种新发现的细胞间通讯机制。已经鉴定出两种不同类型的微泡:膜衍生的小泡 (EVs) 和外泌体。EVs 通过质膜的直接出芽而产生,而外泌体则来源于多泡体的胞吐作用。最近的研究重点集中在 EV 改变邻近细胞表型的能力上,使其类似于产生 EV 的细胞。干细胞是 EV 的丰富来源,干细胞与微环境(即干细胞巢)之间的相互作用在决定干细胞表型方面起着关键作用。干细胞巢假说预测,干细胞数量受到释放自我更新和生存所需信号的巢的可用性的限制,因此巢提供了一种控制和限制干细胞数量的机制。EV 可能通过在细胞之间转移遗传信息在这种情况下发挥着根本作用。EV 可以将 mRNA 和 microRNA 转移到靶细胞,这两者都可能参与靶细胞表型向产生 EV 的细胞的改变。遗传信息的交换可能是双向的,组织损伤后 EV 介导的遗传信息转移可能使干细胞获得损伤组织细胞的表型特征。此外,干细胞衍生的 EV 可能通过促进其重新进入细胞周期并随后增加组织再生的可能性来诱导存活的细胞去分化。

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