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特定 IGFBPs 的表达与再生大鼠比目鱼肌中增殖和分化标志物的表达相关。

Expression of specific IGFBPs is associated with those of the proliferating and differentiating markers in regenerating rat plantaris muscle.

机构信息

Department of Integrated Human Sciences, School of Dentistry, Health Sciences University of Hokkaido, Kanazawa, Ishikari-Tobetsu, Hokkaido, 061-0293, Japan.

Research Center of Physical Fitness, Sports and Health, Toyohashi University of Technology, Toyohashi, Aichi, Japan.

出版信息

J Physiol Sci. 2013 Jan;63(1):71-77. doi: 10.1007/s12576-012-0227-6. Epub 2012 Aug 15.

Abstract

To examine the relationship between specific insulin-like growth factor (IGF)-binding proteins (IGFBPs) and myogenesis during muscle regeneration in vivo, we measured mRNA expression of IGFBPs and myogenic markers in rat plantaris muscle after bupivacaine administration. IGF-I Ea, MGF, IGFBPs and myogenic marker mRNAs were analyzed 12, 24, 48 and 72 h after bupivacaine injection. IGFBP-1, -2, -3 and -4 proteins were immunostained after the treatment. MGF, IGF-I Ea and IGFBP-4 mRNAs started to increase 12 or 24 h after bupivacaine injection and increased further after that. IGFBP-1, -2, -3 and -4 proteins were strongly stained in the immature muscle fiber nuclei and the extracellular matrix after bupivacaine injection. PCNA, MyoD, IGFBP-2 and IGFBP-3 mRNAs increased at 12 or 24 h and did not show further increases after that. Myogenin, p21, IGFBP-1 and IGFBP-5 mRNAs sharply increased after 72 h. These results suggest that specific IGFBPs are individually expressed and differently associated with the expression of myogenic markers in regenerating muscles.

摘要

为了研究体内肌肉再生过程中特定胰岛素样生长因子(IGF)结合蛋白(IGFBPs)与成肌作用的关系,我们在布比卡因给药后测量了大鼠比目鱼肌中 IGFBPs 和肌生成标记物的 mRNA 表达。在布比卡因注射后 12、24、48 和 72 h 分析了 IGF-I Ea、MGF、IGFBPs 和肌生成标记物 mRNAs。在处理后对 IGFBP-1、-2、-3 和 -4 蛋白进行免疫染色。MGF、IGF-I Ea 和 IGFBP-4 mRNAs 在布比卡因注射后 12 或 24 h 开始增加,并在此后进一步增加。IGFBP-1、-2、-3 和 -4 蛋白在布比卡因注射后在未成熟肌纤维核和细胞外基质中强烈染色。PCNA、MyoD、IGFBP-2 和 IGFBP-3 mRNAs 在 12 或 24 h 增加,此后没有进一步增加。Myogenin、p21、IGFBP-1 和 IGFBP-5 mRNAs 在 72 h 后急剧增加。这些结果表明,特定的 IGFBPs 单独表达,并与再生肌肉中肌生成标记物的表达不同相关。

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