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A role for the myogenic determination gene Myf5 in adult regenerative myogenesis.生肌决定基因Myf5在成体再生性肌生成中的作用。
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RAGE expression in rhabdomyosarcoma cells results in myogenic differentiation and reduced proliferation, migration, invasiveness, and tumor growth.横纹肌肉瘤细胞中RAGE的表达导致肌源性分化,并降低增殖、迁移、侵袭能力及肿瘤生长。
Am J Pathol. 2007 Sep;171(3):947-61. doi: 10.2353/ajpath.2007.070049. Epub 2007 Jul 19.
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The amphoterin (HMGB1)/receptor for advanced glycation end products (RAGE) pair modulates myoblast proliferation, apoptosis, adhesiveness, migration, and invasiveness. Functional inactivation of RAGE in L6 myoblasts results in tumor formation in vivo.两性调蛋白(HMGB1)/晚期糖基化终末产物受体(RAGE)对可调节成肌细胞的增殖、凋亡、黏附、迁移和侵袭。L6成肌细胞中RAGE的功能失活会导致体内肿瘤形成。
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Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells.Pax3和Pax7在成体肌肉祖细胞中具有不同但又重叠的功能。
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8
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The p38alpha/beta MAPK functions as a molecular switch to activate the quiescent satellite cell.p38α/β丝裂原活化蛋白激酶作为一种分子开关来激活静止的卫星细胞。
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冻伤及微环境后肌原性蛋白表达的时空变化。

Spatial and temporal changes in myogenic protein expression by the microenvironment after freeze injury.

机构信息

Anatomy Department, University of Otago, Dunedin, New Zealand.

出版信息

J Anat. 2019 Mar;234(3):359-367. doi: 10.1111/joa.12925. Epub 2019 Jan 18.

DOI:10.1111/joa.12925
PMID:30657171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6365476/
Abstract

Skeletal muscle has the remarkable capability to regenerate itself following injury. Adult myogenic stem cells (MSCs) are responsible for the repair and regeneration, and their activity is controlled by intrinsic and extrinsic factors. The aim of this study was to examine and compare the expression levels of Pax3, Pax7, MRF and p38 proteins during the course of regeneration and in different areas of the focal freeze-lesion damaged adult rat TA muscle. Using the focal freeze injury model, immunohistochemistry, laser-capture micro-dissection and Western blot analysis were performed. The results show that (1) in the severely damaged area, the focal freeze-lesion injury significantly activated Pax7 and myogenin expression within 7 days and down-regulated Pax3, MyoD and Myf-5 within 1 or 3 days, and (2) the level of the p38 protein was strongly and transiently up-regulated in the whole muscle on day 7 following injury, whereas the level of the pp38 protein was down-regulated within 3 days in the severely damaged and non-damaged areas. These findings indicate that the temporal (e.g. the time course of regeneration) and spatial (e.g. three zones created by the focal freeze-lesion) cues in a regenerating muscle have a significant impact on the activity of the adult MSCs.

摘要

骨骼肌具有在损伤后自我再生的显著能力。成肌干细胞(MSCs)负责修复和再生,其活性受内在和外在因素的控制。本研究旨在探讨和比较 Pax3、Pax7、MRF 和 p38 蛋白在再生过程中和在焦点冷冻损伤成年大鼠 TA 肌肉不同区域中的表达水平。使用焦点冷冻损伤模型,进行了免疫组织化学、激光捕获微切割和 Western blot 分析。结果表明:(1)在严重损伤区,焦点冷冻损伤在 7 天内显著激活 Pax7 和肌生成素表达,并在 1 或 3 天内下调 Pax3、MyoD 和 Myf-5;(2)损伤后第 7 天,整个肌肉中 p38 蛋白水平强烈且短暂地上调,而 pp38 蛋白水平在严重损伤区和未损伤区均在 3 天内下调。这些发现表明,再生肌肉中的时间(例如再生的时间过程)和空间(例如焦点冷冻损伤形成的三个区域)线索对成体 MSCs 的活性有重要影响。