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在慢性骨骼肌超负荷期间,PAX3/7的表达与MyoD一致。

PAX3/7 expression coincides with MyoD during chronic skeletal muscle overload.

作者信息

Hyatt Jon-Philippe K, McCall Gary E, Kander Elizabeth M, Zhong Hui, Roy Roland R, Huey Kimberly A

机构信息

Department of Human Science, School of Nursing and Health Studies, Georgetown University, 3700 Reservoir Rd., Washington, DC 20057, USA.

出版信息

Muscle Nerve. 2008 Jul;38(1):861-6. doi: 10.1002/mus.21006.

Abstract

Paired box (Pax) proteins 3 and 7 are key determinants for embryonic skeletal muscle development by initiating myogenic regulatory factor (MRF) gene expression. We show that Pax3 and 7 participate in adult skeletal muscle plasticity during the initial responses to chronic overload (< or =7 days) and appear to coordinate MyoD expression, a member of the MRF family of genes. Pax3 and 7 mRNA were higher than control within 12 h after initiation of overload, preceded the increase in MyoD mRNA on day 1, and peaked on day 2. On days 3 and 7, Pax7 mRNA remained higher than control, suggesting that satellite cell self-renewal was occurring. Pax3 and 7 and MyoD protein levels were higher than control on days 2 and 3. These data indicate that Pax3 and 7 coordinate the recapitulation of developmental-like regulatory mechanisms in response to growth-inducing stimuli in adult skeletal muscle, presumably through activation of satellite cells.

摘要

配对盒(Pax)蛋白3和7是通过启动肌源性调节因子(MRF)基因表达来决定胚胎骨骼肌发育的关键因素。我们发现,在对慢性超负荷(≤7天)的初始反应过程中,Pax3和7参与成年骨骼肌可塑性的调节,并且似乎协同调节MRF基因家族成员之一的MyoD的表达。在超负荷开始后的12小时内,Pax3和7的mRNA水平高于对照组,在第1天MyoD mRNA增加之前就已升高,并在第2天达到峰值。在第3天和第7天,Pax7 mRNA水平仍高于对照组,表明卫星细胞正在进行自我更新。在第2天和第3天,Pax3、7以及MyoD的蛋白水平高于对照组。这些数据表明,Pax3和7可能通过激活卫星细胞,协同调节成年骨骼肌中类似发育的调节机制,以应对生长诱导刺激。

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