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凋亡细胞外囊泡携带 Mif 调节组织维持过程中邻近上皮干细胞中巨噬细胞的募集和代偿性增殖。

Apoptotic extracellular vesicles carrying Mif regulate macrophage recruitment and compensatory proliferation in neighboring epithelial stem cells during tissue maintenance.

机构信息

Genetics and Epigenetics Graduate Program, The University of Texas MD Anderson Cancer Center UT Health Houston Graduate School of Biomedical Sciences, Houston, Texas, United States of America.

Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.

出版信息

PLoS Biol. 2024 Nov 4;22(11):e3002194. doi: 10.1371/journal.pbio.3002194. eCollection 2024 Nov.

Abstract

Apoptotic cells can signal to neighboring cells to stimulate proliferation and compensate for cell loss to maintain tissue homeostasis. While apoptotic cell-derived extracellular vesicles (AEVs) can transmit instructional cues to mediate communication with neighboring cells, the molecular mechanisms that induce cell division are not well understood. Here, we show that macrophage migration inhibitory factor (Mif)-containing AEVs regulate compensatory proliferation via ERK signaling in epithelial stem cells of larval zebrafish. Time-lapse imaging showed efferocytosis of AEVs from dying epithelial stem cells by healthy neighboring stem cells. Proteomic and ultrastructure analysis of purified AEVs identified Mif localization on the AEV surface. Pharmacological inhibition or genetic mutation of Mif, or its cognate receptor CD74, decreased levels of phosphorylated ERK and compensatory proliferation in the neighboring epithelial stem cells. Disruption of Mif activity also caused decreased numbers of macrophages patrolling near AEVs, while depletion of the macrophage lineage resulted in a reduced proliferative response by the epithelial stem cells. We propose that AEVs carrying Mif directly stimulate epithelial stem cell repopulation and guide macrophages to cell non-autonomously induce localized proliferation to sustain overall cell numbers during tissue maintenance.

摘要

凋亡细胞可以向邻近细胞发出信号,刺激增殖并补偿细胞损失,以维持组织内稳态。凋亡细胞来源的细胞外囊泡 (EVs) 可以传递指导信号,介导与邻近细胞的通讯,但其诱导细胞分裂的分子机制尚不清楚。在这里,我们显示巨噬细胞移动抑制因子 (Mif) 包含的 EVs 通过 ERK 信号在幼虫斑马鱼的上皮干细胞中调节代偿性增殖。延时成像显示,健康的邻近干细胞从死亡的上皮干细胞中吞噬 EVs。纯化 EVs 的蛋白质组学和超微结构分析鉴定出 Mif 在 EV 表面的定位。Mif 的药理学抑制或基因突变,或其同源受体 CD74,降低了邻近上皮干细胞中磷酸化 ERK 和代偿性增殖的水平。Mif 活性的破坏也导致了在 EV 附近巡逻的巨噬细胞数量减少,而巨噬细胞谱系的耗竭导致上皮干细胞的增殖反应减少。我们提出,携带 Mif 的 EVs 直接刺激上皮干细胞的再增殖,并指导巨噬细胞通过非自主方式诱导局部增殖,以维持组织维持过程中的总体细胞数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/727f/11578469/7dcdae766765/pbio.3002194.g001.jpg

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