不同激酶在毒蕈碱M3受体介导的大鼠结肠纵肌收缩中的作用。

Q3 Medicine
Charles D Anderson, Derek M Kendig, Mohammad Al-Qudah, Sunila Mahavadi, Karnam S Murthy, John R Grider
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引用次数: 9

摘要

肠内纵肌层在蠕动过程中与圆肌层在功能上是对立的。各层神经支配的差异允许一层收缩的同时另一层放松,使肠道内容物以受控的方式通过。发育的差异使两层细胞在受体数量、膜脂处理和钙处理概况/行为上存在差异。纵肌的收缩活动主要是由来自肌丛的胆碱能神经输入介导的。毒蕈碱受体的激活导致几种激酶的快速激活,包括MLC激酶、ERK1/2、CaMKII和Rho激酶。肌球蛋白轻链(MLC20)被MLC激酶(MLCK)磷酸化是圆形和纵向肌细胞收缩的先决条件。在大鼠结肠纵肌条中,我们用激酶抑制剂孵育后测量了毒蕈碱受体介导的收缩。Rho激酶、ERK1/2、CaMKII和CaMKK对基底张力的调节存在差异。Rho激酶、ERK1/2、CaMKK/AMPK和CaMKII的选择性抑制剂均可减少碳水化合物诱导的神经支配肌条收缩。这些抑制剂对MLCK活性无直接影响。因此,与先前报道的CaMKII和ERK1/2不参与收缩的分离肌肉细胞不同,我们得出结论,在神经支配的纵肌条中,碳水化合物诱导的收缩调节涉及Rho激酶、ERK1/2、CaMKK/AMPK和CaMKII的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon.

Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon.

Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon.

Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon.

The longitudinal muscle layer in gut is the functional opponent to the circular muscle layer during peristalsis. Differences in innervation of the layers allow for the contraction of one layer concurrently with the relaxation of the other, enabling the passage of gut contents in a controlled fashion. Differences in development have given the cells of the two layers differences in receptor populations, membrane lipid handling, and calcium handling profiles/behaviors. The contractile activity of the longitudinal muscle is largely mediated by cholinergic neural input from myenteric plexus. Activation of muscarinic receptors leads to rapid activation of several kinases including MLC kinase, ERK1/2, CaMKII and Rho kinase. Phosphorylation of myosin light chain (MLC20) by MLC kinase (MLCK) is a prerequisite for contraction in both circular and longitudinal muscle cells. In rat colonic longitudinal muscle strips, we measured muscarinic receptor-mediated contraction following incubation with kinase inhibitors. Basal tension was differentially regulated by Rho kinase, ERK1/2, CaMKII and CaMKK. Selective inhibitors of Rho kinase, ERK1/2, CaMKK/AMPK, and CaMKII each reduced carbachol-induced contraction in the innervated muscle strips. These inhibitors had no direct effect on MLCK activity. Thus unlike previously reported for isolated muscle cells where CaMKII and ERK1/2 are not involved in contraction, we conclude that the regulation of carbachol-induced contraction in innervated longitudinal muscle strips involves the interplay of Rho kinase, ERK1/2, CaMKK/AMPK, and CAMKII.

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来源期刊
Journal of Smooth Muscle Research
Journal of Smooth Muscle Research Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
2.30
自引率
0.00%
发文量
7
审稿时长
10 weeks
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