首页> 外文期刊>The Journal of Physiology >Tumour necrosis factor-alpha activates a calcium sensitization pathway in guinea-pig bronchial smooth muscle.
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Tumour necrosis factor-alpha activates a calcium sensitization pathway in guinea-pig bronchial smooth muscle.

机译:肿瘤坏死因子-α激活豚鼠支气管平滑肌中的钙敏化途径。

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摘要

1. The effects of tumour necrosis factor-alpha (TNF) on guinea-pig bronchial smooth muscle contractility were investigated. 2. The Ca2+-activated contractile response of permeabilized bronchial smooth muscle strips was significantly increased after incubation with 1 microgram ml-1 TNF for 45 min. This TNF-induced effect was not due to a further increase in intracellular Ca2+. 3. The TNF-induced Ca2+ sensitization was, at least partly, the result of an increase in myosin light chain20 phosphorylation. 4. The intracellular signalling pathway involved in this effect of TNF was further investigated. Sphingomyelinase, a potential mediator of TNF, had no effect on Ca2+ sensitivity of permeabilized bronchial smooth muscle. Also, p42/p44 mitogen-activated protein kinase (p42/p44mapk), activated by TNF in some cell types, did not show an increased activation in bronchial smooth muscle after TNF treatment. 5. In conclusion, TNF may activate a novel signalling pathway in guinea-pig bronchial smooth muscle leading to an increase in myosin light chain20 phosphorylation and a subsequent increase in Ca2+ sensitivity of the myofilaments. This pathway does not appear to involve sphingomyelinase-liberated ceramides or activation of p42/p44mapk. Given the importance of TNF in asthma, this TNF-induced Ca2+ sensitization of the myofilaments may represent a mechanism responsible for airway hyper-responsiveness.
机译:1.研究了肿瘤坏死因子-α(TNF)对豚鼠支气管平滑肌收缩力的影响。 2.与1微克ml-1 TNF孵育45分钟后,透化的支气管平滑肌条的Ca2 +激活的收缩反应显着增加。 TNF诱导的作用不是由于细胞内Ca2 +的进一步增加。 3. TNF诱导的Ca2 +致敏至少部分是肌球蛋白轻链20磷酸化增加的结果。 4.进一步研究了与TNF的这种作用有关的细胞内信号传导途径。鞘磷脂酶(一种潜在的TNF介导剂)对通透性支气管平滑肌的Ca2 +敏感性没有影响。同样,在某些细胞类型中,TNF激活的p42 / p44丝裂原激活蛋白激酶(p42 / p44mapk)在TNF治疗后未显示出支气管平滑肌激活增加。 5.总之,TNF可能会激活豚鼠支气管平滑肌中的新信号传导途径,导致肌球蛋白轻链20磷酸化增加,并随后增加肌丝的Ca2 +敏感性。该途径似乎不涉及鞘磷脂酶释放的神经酰胺或p42 / p44mapk的激活。考虑到TNF在哮喘中的重要性,这种TNF诱导的肌丝Ca2 +致敏作用可能是导致气道高反应性的机制。

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