Biomaterial and stem cell‐based strategies for skeletal muscle regeneration

干细胞 再生(生物学) 间充质干细胞 祖细胞 细胞生物学 成体干细胞 骨骼肌 干细胞移植修复关节软骨 生物 医学 免疫学 内皮干细胞 解剖 体外 生物化学
作者
Andrew J. Dunn,Muhamed Talovic,Krishna H. Patel,Anjali Patel,Madison Marcinczyk,Koyal Garg
出处
期刊:Journal of Orthopaedic Research [Wiley]
卷期号:37 (6): 1246-1262 被引量:75
标识
DOI:10.1002/jor.24212
摘要

ABSTRACT Adult skeletal muscle can regenerate effectively after mild physical or chemical insult. Muscle trauma or disease can overwhelm this innate capacity for regeneration and result in heightened inflammation and fibrotic tissue deposition resulting in loss of structure and function. Recent studies have focused on biomaterial and stem cell‐based therapies to promote skeletal muscle regeneration following injury and disease. Many stem cell populations besides satellite cells are implicated in muscle regeneration. These stem cells include but are not limited to mesenchymal stem cells, adipose‐derived stem cells, hematopoietic stem cells, pericytes, fibroadipogenic progenitors, side population cells, and CD133 + stem cells. However, several challenges associated with their isolation, availability, delivery, survival, engraftment, and differentiation have been reported in recent studies. While acellular scaffolds offer a relatively safe and potentially off‐the‐shelf solution to cell‐based therapies, they are often unable to stimulate host cell migration and activity to a level that would result in clinically meaningful regeneration of traumatized muscle. Combining stem cells and biomaterials may offer a viable therapeutic strategy that may overcome the limitations associated with these therapies when they are used in isolation. In this article, we review the stem cell populations that can stimulate muscle regeneration in vitro and in vivo. We also discuss the regenerative potential of combination therapies that utilize both stem cell and biomaterials for the treatment of skeletal muscle injury and disease. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:1246–1262, 2019.

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