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大鼠喉内肌再支配后卫星细胞活性及肌分化抗原(MyoD)的调节

Modulation of satellite cells activity and MyoD in rat thyroarytenoid muscle after reinnervation.

作者信息

Kodama Haruka, Kumai Yoshihiko, Nishimoto Kohei, Sanuki Tetsuji, Yumoto Eiji

机构信息

Department of Otolaryngology Head and Neck Surgery, Kumamoto University, Graduate School of Medicine, Kumamoto, Japan.

出版信息

Laryngoscope. 2015 Jul;125(7):E245-51. doi: 10.1002/lary.25248. Epub 2015 Mar 26.

Abstract

OBJECTIVES/HYPOTHESIS: To examine modulation of M-cadherin, a marker for satellite cells (SCs); and MyoD, which may indicate the myogenic activity following recurrent laryngeal nerve (RLN) denervation and immediate reinnervation; and to elucidate the correlation between their modulations and establishment of neuromuscular junctions (NMJs) in the reinnervated rat thyroarytenoid (TA) muscle.

STUDY DESIGN

Quantitative real-time polymerase chain reaction qPCR and histologic assessment of the TA muscle following RLN transection and anastomosis.

METHODS

Rats were divided into three groups: 1) denervation alone (DNV) (n = 60), 2) denervation with anastomosis (ANS) (n = 60), and 3) sham-operated controls (n = 12). Animals were sacrificed at 3 days and 1, 3, and 5 weeks after treatment. TA muscles harvested from 40 animals from each DNV and ANS group; all of sham group were subjected to qPCR for assessment of the modulation of M-cadherin and MyoD; and the remaining larynges of DNV and ANS group were used for histologic analysis.

RESULTS

The expression levels of messenger RNAs (mRNAs) encoding M-cadherin and MyoD in the TA muscle of the DNV group were significantly higher (P < 0.05) than in the control throughout the study period. These mRNA levels in the ANS group were significantly higher (P < 0.05) at ≤ 1 week than in the controls but fell to control levels at ≥ 3 weeks. In the ANS group, recovery of muscle area and NMJs structure occurred by 3 weeks.

CONCLUSION

These data suggested that NMJ formation following reinnervation might prompt recovery of M-cadherin and MyoD mRNA expression to the quiescent level of SCs.

摘要

目的/假设:研究卫星细胞(SCs)标志物M-钙黏蛋白的调节情况;以及肌分化抗原(MyoD),其可能指示喉返神经(RLN)去神经支配及即刻再支配后的生肌活性;并阐明它们的调节与再支配大鼠甲杓肌(TA)中神经肌肉接头(NMJs)建立之间的相关性。

研究设计

对RLN横断和吻合术后的TA肌进行定量实时聚合酶链反应(qPCR)和组织学评估。

方法

将大鼠分为三组:1)单纯去神经支配组(DNV)(n = 60),2)去神经支配并吻合组(ANS)(n = 60),3)假手术对照组(n = 12)。在治疗后3天、1周、3周和5周处死动物。从每个DNV组和ANS组的40只动物中采集TA肌;对所有假手术组进行qPCR以评估M-钙黏蛋白和MyoD的调节情况;DNV组和ANS组其余的喉部用于组织学分析。

结果

在整个研究期间,DNV组TA肌中编码M-钙黏蛋白和MyoD的信使核糖核酸(mRNAs)表达水平显著高于对照组(P < 0.05)。ANS组中这些mRNA水平在≤1周时显著高于对照组(P < 0.05),但在≥3周时降至对照水平。在ANS组中,肌肉面积和NMJs结构在3周时恢复。

结论

这些数据表明,再支配后NMJ的形成可能促使M-钙黏蛋白和MyoD mRNA表达恢复到SCs的静止水平。

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