Department of Surgery, Division of Plastic and Reconstructive Surgery, University of California, San Francisco, CA 94143, USA.
Department of Otolaryngology - Head and Neck Surgery, University of California, San Francisco, CA 94143, USA.
Stem Cell Reports. 2018 Mar 13;10(3):1160-1174. doi: 10.1016/j.stemcr.2018.01.022. Epub 2018 Mar 1.
Investigation of human muscle regeneration requires robust methods to purify and transplant muscle stem and progenitor cells that collectively constitute the human satellite cell (HuSC) pool. Existing approaches have yet to make HuSCs widely accessible for researchers, and as a result human muscle stem cell research has advanced slowly. Here, we describe a robust and predictable HuSC purification process that is effective for each human skeletal muscle tested and the development of storage protocols and transplantation models in dystrophin-deficient and wild-type recipients. Enzymatic digestion, magnetic column depletion, and 6-marker flow-cytometric purification enable separation of 10 highly enriched HuSCs per gram of muscle. Cryostorage of HuSCs preserves viability, phenotype, and transplantation potential. Development of enhanced and species-specific transplantation protocols enabled serial HuSC xenotransplantation and recovery. These protocols and models provide an accessible system for basic and translational investigation and clinical development of HuSCs.
研究人类肌肉再生需要强大的方法来纯化和移植肌肉干细胞和祖细胞,这些细胞共同构成了人类卫星细胞(HuSC)池。现有的方法还没有使 HuSCs 广泛应用于研究人员,因此人类肌肉干细胞研究进展缓慢。在这里,我们描述了一种强大且可预测的 HuSC 纯化过程,该过程对每种测试的人类骨骼肌都有效,并为在营养不良型和野生型受体中开发储存方案和移植模型奠定了基础。酶消化、磁性柱耗尽和 6 标记流式细胞术纯化可分离每克肌肉中 10 个高度富集的 HuSCs。HuSCs 的低温储存保存了其活力、表型和移植潜能。增强和种间特异性移植方案的开发使 HuSC 的连续异种移植和恢复成为可能。这些方案和模型为 HuSCs 的基础和转化研究以及临床开发提供了一个易于使用的系统。