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肌肉干细胞坏死的表观遗传抑制减弱是肌肉营养不良有效再生所必需的。

Attenuated Epigenetic Suppression of Muscle Stem Cell Necroptosis Is Required for Efficient Regeneration of Dystrophic Muscles.

机构信息

Department of Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.

Department of Pharmacology, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.

出版信息

Cell Rep. 2020 May 19;31(7):107652. doi: 10.1016/j.celrep.2020.107652.

Abstract

Somatic stem cells expand massively during tissue regeneration, which might require control of cell fitness, allowing elimination of non-competitive, potentially harmful cells. How or if such cells are removed to restore organ function is not fully understood. Here, we show that a substantial fraction of muscle stem cells (MuSCs) undergo necroptosis because of epigenetic rewiring during chronic skeletal muscle regeneration, which is required for efficient regeneration of dystrophic muscles. Inhibition of necroptosis strongly enhances suppression of MuSC expansion in a non-cell-autonomous manner. Prevention of necroptosis in MuSCs of healthy muscles is mediated by the chromatin remodeler CHD4, which directly represses the necroptotic effector Ripk3, while CHD4-dependent Ripk3 repression is dramatically attenuated in dystrophic muscles. Loss of Ripk3 repression by inactivation of Chd4 causes massive necroptosis of MuSCs, abolishing regeneration. Our study demonstrates how programmed cell death in MuSCs is tightly controlled to achieve optimal tissue regeneration.

摘要

体干细胞在组织再生过程中会大量扩增,这可能需要控制细胞的适应性,从而清除非竞争的、潜在有害的细胞。但目前尚不完全清楚细胞是如何被清除以恢复器官功能的。本文中,作者发现由于慢性骨骼肌再生过程中的表观遗传重排,大量的肌肉干细胞(MuSCs)会发生坏死性凋亡,这对于营养不良肌肉的有效再生是必需的。坏死性凋亡的抑制会以非细胞自主的方式强烈增强对 MuSC 扩增的抑制。健康肌肉中 MuSCs 的坏死性凋亡的预防是由染色质重塑因子 CHD4 介导的,它直接抑制坏死性凋亡效应因子 Ripk3,而在营养不良的肌肉中,CHD4 依赖性的 Ripk3 抑制作用显著减弱。通过失活 Chd4 而导致 Ripk3 抑制的丧失会引起 MuSCs 的大量坏死性凋亡,从而阻止了再生。本研究展示了 MuSCs 中程序性细胞死亡是如何被严格控制以实现最佳组织再生的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d25/7242912/b66bbc0bc157/fx1.jpg

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