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血小板衍生的具有呼吸功能的线粒体转移至间充质干细胞,通过代谢重编程促进伤口愈合。

Platelet-derived respiratory-competent mitochondria transfer to mesenchymal stem cells to promote wound healing via metabolic reprogramming.

作者信息

Chen Enlin, Chen Zhe, Chen Linxi, Hu Xiaoling

机构信息

Department of Anesthesiology, The First Affiliated Hospital of University of South China, Hengyang, Hunan, China.

Institute of Pharmacy and Pharmacology, Hunan Provincial Key Laboratory of Tumor Microenvironment Responsive Drug Research, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, College of Basic Medical Science, Hengyang Medical School, University of South China, Hengyang, Hunan, China.

出版信息

Platelets. 2022 Feb 17;33(2):171-173. doi: 10.1080/09537104.2021.1961717. Epub 2022 Feb 3.

Abstract

Mitochondria regulate intracellular metabolism and are also involved in intercellular transfer in and in , thereby affecting the function of adjacent cells. Mitochondria can also be transferred to various differentiated cells to improve their respiratory function, ATP production, as well as protect damaged cells from apoptosis. Both in and in , mitochondria can be transferred from one cell to another to regulate cellular metabolism under physiological or pathophysiological conditions, referred to as "mitochondrial translocation". Mitochondrial translocation is associated in various situations such as repairing damaged cells, promoting cancer progression and enhancing chemoresistance. Platelets contain mitochondria that promote energy metabolism and various growth factors, thus playing an important role in pathophysiological processes such as thrombosis, hemostasis, inflammation and wound healing. Current studies suggest that mesenchymal stem cells (MSCs) can communicate with their microenvironment through bidirectional alternation of mitochondria to improve their wound healing capacity. Platelets or platelet-containing preparations such as platelet-rich plasma (PRP) can stimulate the proliferation and pro-angiogenic properties of MSCs under oxidative stress to enhance their survival. Recent studies by Levoux et al. have shown that activated platelet-derived mitochondria have the respiratory capacity to translocate to MSCs and stimulate the pro-angiogenic properties of MSCs through metabolic reprogramming, thereby promoting angiogenesis and wound healing. The mechanism of mitochondrial internalization of cells and energy metabolism is a new example of mitochondrial translocation altering somatic cell behavior and viability. Therefore, we aim to comment the mechanisms of platelet mitochondrial translocation and metabolic reprogramming of MSCs, suggesting that platelets or platelet-containing preparations such as platelet-rich plasma (PRP) may provide a practical guide for tissue injury treatment.

摘要

线粒体调节细胞内代谢,还参与细胞间的物质传递,从而影响相邻细胞的功能。线粒体也可转移至各种分化细胞,以改善其呼吸功能、ATP生成,并保护受损细胞免于凋亡。在体内和体外,线粒体均可从一个细胞转移至另一个细胞,在生理或病理生理条件下调节细胞代谢,这一过程称为“线粒体易位”。线粒体易位与多种情况相关,如修复受损细胞、促进癌症进展及增强化疗耐药性。血小板含有促进能量代谢的线粒体和多种生长因子,因此在血栓形成、止血、炎症及伤口愈合等病理生理过程中发挥重要作用。目前的研究表明,间充质干细胞(MSCs)可通过线粒体的双向交换与其微环境进行沟通,以提高其伤口愈合能力。血小板或含血小板制剂,如富血小板血浆(PRP),可在氧化应激下刺激MSCs的增殖和促血管生成特性,以提高其存活率。Levoux等人最近的研究表明,活化的血小板源性线粒体具有转移至MSCs的呼吸能力,并通过代谢重编程刺激MSCs的促血管生成特性,从而促进血管生成和伤口愈合。细胞线粒体内化及能量代谢的机制是线粒体易位改变体细胞行为和活力的一个新例证。因此,我们旨在阐述血小板线粒体易位及MSCs代谢重编程的机制,提示血小板或含血小板制剂,如富血小板血浆(PRP),可能为组织损伤治疗提供实用指导。

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