Department of Kinesiology and Community Health, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
FASEB J. 2019 Jun;33(6):7694-7706. doi: 10.1096/fj.201802580R. Epub 2019 Apr 25.
Conditions of extended bed rest and limb immobilization can initiate rapid and significant loss of skeletal muscle mass and function. Physical rehabilitation is standard practice following a period of disuse, yet mobility may be severely compromised, and recovery is commonly delayed or incomplete in special populations. Thus, a novel approach toward recovery of muscle mass is highly desired. Pericytes [neuron-glial antigen 2 (NG2)CD31CD45 (Lineage [Lin]) and CD146Lin] demonstrate capacity to facilitate muscle repair, yet the ability to enhance myofiber growth following disuse is unknown. In the current study, 3-4-mo-old mice were unilaterally immobilized for 14 d (IM) or immobilized for 14 d followed by 14 d of remobilization (RE). Flow cytometry and targeted gene expression analyses were completed to assess pericyte quantity and function following IM and RE. In addition, a transplantation study was conducted to assess the impact of pericytes on recovery. Results from targeted analyses suggest minimal impact of disuse on pericyte gene expression, yet NG2Lin pericyte quantity is reduced following IM ( < 0.05). Remarkably, pericyte transplantation recovered losses in myofiber cross-sectional area and the capillary-to-fiber ratio following RE, whereas deficits remained with vehicle alone ( = 0.01). These findings provide the first evidence that pericytes effectively rehabilitate skeletal muscle mass following disuse atrophy.-Munroe, M., Dvoretskiy, S., Lopez, A., Leong, J., Dyle, M. C., Kong, H., Adams, C. M., Boppart, M. D. Pericyte transplantation improves skeletal muscle recovery following hindlimb immobilization.
延长卧床休息和肢体固定的条件会导致骨骼肌迅速而显著地减少和功能丧失。在一段时间的不活动后,身体康复是标准的做法,但活动能力可能严重受损,在特殊人群中,康复通常会延迟或不完全。因此,非常需要一种新的方法来恢复肌肉量。周细胞[神经元-神经胶质抗原 2(NG2)CD31CD45(谱系[Lin])和 CD146Lin]具有促进肌肉修复的能力,但在失用后增强肌纤维生长的能力尚不清楚。在本研究中,3-4 个月大的小鼠单侧固定 14 天(IM)或固定 14 天后再固定 14 天(RE)。进行流式细胞术和靶向基因表达分析,以评估 IM 和 RE 后周细胞的数量和功能。此外,还进行了一项移植研究,以评估周细胞对恢复的影响。靶向分析的结果表明,失用对周细胞基因表达的影响很小,但 IM 后 NG2Lin 周细胞数量减少(<0.05)。值得注意的是,周细胞移植可恢复 RE 后肌纤维横截面积和毛细血管与纤维比的损失,而单独使用载体则保持不变(=0.01)。这些发现首次提供了证据表明,周细胞在失用性萎缩后有效地恢复骨骼肌量。