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本文引用的文献

1
Physical strategies to prevent disuse-induced functional decline in the elderly.预防老年人因不活动导致功能下降的身体策略。
Ageing Res Rev. 2018 Nov;47:80-88. doi: 10.1016/j.arr.2018.07.003. Epub 2018 Jul 18.
2
A molecular atlas of cell types and zonation in the brain vasculature.大脑血管的细胞类型和分区的分子图谱。
Nature. 2018 Feb 22;554(7693):475-480. doi: 10.1038/nature25739. Epub 2018 Feb 14.
3
Type 2 diabetes impairs the ability of skeletal muscle pericytes to augment postischemic neovascularization in db/db mice.2 型糖尿病削弱了 db/db 小鼠骨骼肌周细胞在缺血后增强新血管生成的能力。
Am J Physiol Cell Physiol. 2018 May 1;314(5):C534-C544. doi: 10.1152/ajpcell.00158.2017. Epub 2018 Jan 10.
4
The impact of mechanically stimulated muscle-derived stromal cells on aged skeletal muscle.机械刺激的肌源性基质细胞对衰老骨骼肌的影响。
Exp Gerontol. 2018 Mar;103:35-46. doi: 10.1016/j.exger.2017.12.012. Epub 2017 Dec 18.
5
Differential requirement for satellite cells during overload-induced muscle hypertrophy in growing versus mature mice.生长和成熟小鼠在超负荷诱导的肌肉肥大过程中卫星细胞的差异需求。
Skelet Muscle. 2017 Jul 10;7(1):14. doi: 10.1186/s13395-017-0132-z.
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Role of ATF4 in skeletal muscle atrophy.ATF4在骨骼肌萎缩中的作用。
Curr Opin Clin Nutr Metab Care. 2017 May;20(3):164-168. doi: 10.1097/MCO.0000000000000362.
7
αβ Integrin regulation of gene transcription in skeletal muscle following an acute bout of eccentric exercise.急性离心运动后骨骼肌中αβ整合素对基因转录的调控
Am J Physiol Cell Physiol. 2017 May 1;312(5):C638-C650. doi: 10.1152/ajpcell.00106.2016. Epub 2017 Mar 8.
8
Perivascular Stem Cells Diminish Muscle Atrophy Following Massive Rotator Cuff Tears in a Small Animal Model.在小动物模型中,血管周围干细胞可减轻巨大肩袖撕裂后的肌肉萎缩。
J Bone Joint Surg Am. 2017 Feb 15;99(4):331-341. doi: 10.2106/JBJS.16.00645.
9
Requirement of myomaker-mediated stem cell fusion for skeletal muscle hypertrophy.骨骼肌肥大对肌生成素介导的干细胞融合的需求。
Elife. 2017 Feb 10;6:e20007. doi: 10.7554/eLife.20007.
10
Pericytes of Multiple Organs Do Not Behave as Mesenchymal Stem Cells In Vivo.多器官的周细胞在体内并非表现为间充质干细胞。
Cell Stem Cell. 2017 Mar 2;20(3):345-359.e5. doi: 10.1016/j.stem.2016.12.006. Epub 2017 Jan 19.

周细胞移植可改善后肢固定后骨骼肌的恢复。

Pericyte transplantation improves skeletal muscle recovery following hindlimb immobilization.

机构信息

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.

出版信息

FASEB J. 2019 Jun;33(6):7694-7706. doi: 10.1096/fj.201802580R. Epub 2019 Apr 25.

DOI:10.1096/fj.201802580R
PMID:31021652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6529341/
Abstract

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.

摘要

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。