Metabolomics-guided isolation of myogenic progenitor cells for improved transplantation.

IF 5.4 2区 生物学 Q2 CELL BIOLOGY
Lauren K McKay, Christopher G Vann, James R Bain, Shihuan Kuang, Christopher B Newgard, James P White, David E Lee
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Abstract

Skeletal muscle maintains considerable capacity for regeneration following injury, but successful regeneration is limited in instances of volumetric muscle loss, advanced aging, or muscular dystrophies. Considerable research has been done on muscle stem cell (MuSC) transplantation; however, proliferative exhaustion and donor cell dose requirements have slowed progress. Due to the paramount role of cellular metabolism in regenerative function of stem cells, the clinical potential for MuSC therapy may be improved by minimizing the isolation-induced metabolic perturbations experienced by MuSCs. This study uses a model of simulated cell sorting combined with untargeted, small-molecule metabolomic profiling to outline sorting-induced metabolic perturbations in C2C12 myoblasts. We expand upon this by performing a time course of metabolomic profiling on myoblasts recovering from either fluorescence-activated cell sorting or magnetic-bead-activated cell sorting-based isolation procedures to determine the method and recovery timing for optimal redox and energetic status. Using this metabolism-informed method, we then performed primary MuSC transplantation studies in mice to demonstrate the generalizability from the in vitro system to in vivo MuSC transplantation during regeneration from barium chloride-induced injury. Our findings demonstrate metabolically favorable strategies to isolate MuSC for analysis of the quiescent-to-activated metabolic transition or enhance transplantation efficacy.NEW & NOTEWORTHY Due to the paramount role of cellular metabolism in regenerative function of stem cells, the clinical potential for muscle stem cell (MuSC) therapy may be improved by minimizing isolation-induced metabolic perturbations. This study uses a model of simulated cell sorting combined with untargeted, small-molecule metabolomic profiling to outline sorting-induced metabolic perturbations in myoblasts. Our findings demonstrate metabolically favorable strategies to isolate MuSC for analysis of the quiescent-to-activated metabolic transition or enhance transplantation efficacy.

代谢组学引导下肌源性祖细胞的分离用于改良移植。
骨骼肌在损伤后保持相当大的再生能力,但在体积性肌肉损失、衰老或肌肉营养不良的情况下,成功的再生是有限的。肌肉干细胞(MuSC)移植的研究已经相当多;然而,增殖衰竭和供体细胞剂量要求延缓了进展。由于细胞代谢在干细胞再生功能中的重要作用,通过尽量减少分离诱导的MuSC代谢扰动,可以提高MuSC治疗的临床潜力。本研究使用模拟细胞分选模型结合非靶向小分子代谢组学分析来概述C2C12成肌细胞分选诱导的代谢扰动。在此基础上,我们对从荧光活化细胞分选(FACS)或磁珠活化细胞分选(MACS)分离过程中恢复的成肌细胞进行了代谢组学分析,以确定最佳氧化还原和能量状态的方法和恢复时间。利用这种代谢相关的方法,我们在小鼠身上进行了MuSC移植研究,以证明在bacl2诱导的损伤再生过程中,从体外系统到体内MuSC移植的普遍性。我们的研究结果证明了分离MuSC的代谢有利策略,以分析静止到激活的代谢转变或增强移植疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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