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首页> 外文期刊>American Journal of Physiology >Hypotonic swelling-induced Ca(2+) release by an IP(3)-insensitive Ca(2+) store.
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Hypotonic swelling-induced Ca(2+) release by an IP(3)-insensitive Ca(2+) store.

机译:低渗性肿胀诱导的Ca(2+)释放的IP(3)不敏感的Ca(2+)存储。

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Hypotonic swelling increases the intracellular Ca(2+) concentration ([Ca(2+)](i)) in vascular smooth muscle cells (VSMC). The source of this Ca(2+) is not clear. To study the source of increase in [Ca(2+)](i) in response to hypotonic swelling, we measured [Ca(2+)](i) in fura 2-loaded cultured VSMC (A7r5 cells). Hypotonic swelling produced a 40.7-nM increase in [Ca(2+)](i) that was not inhibited by EGTA but was inhibited by 1 microM thapsigargin. Prior depletion of inositol 1,4,5-trisphosphate (IP(3))-sensitive Ca(2+) stores with vasopressin did not inhibit the increase in [Ca(2+)](i) in response to hypotonic swelling. Exposure of (45)Ca(2+)-loaded intracellular stores to hypotonic swelling in permeabilized VSMC produced an increase in (45)Ca(2+) efflux, which was inhibited by 1 microM thapsigargin but not by 50 microg/ml heparin, 50 microM ruthenium red, or 25 microM thio-NADP. Thus hypotonic swelling of VSMC causes a release of Ca(2+) from the intracellular stores from a novel site distinct from the IP(3)-, ryanodine-, and nicotinic acid adenine dinucleotide phosphate-sensitive stores.
机译:低渗性肿胀会增加血管平滑肌细胞(VSMC)中的细胞内Ca(2+)浓度([Ca(2 +)](i))。该Ca(2+)的来源尚不清楚。要研究低渗性肿胀中[Ca(2 +)](i)增加的来源,我们在装有呋喃2的培养的VSMC(A7r5细胞)中测量了[Ca(2 +)](i)。低渗性肿胀产生[Ca(2 +)](i)增加40.7-nM,这不受EGTA抑制,但被1 microM毒胡萝卜素抑制。先前消耗的肌醇1,4,5-三磷酸(IP(3))敏感的Ca(2+)存储与加压素未抑制[Ca(2 +)](i)对低渗肿胀的反应。 (45)Ca(2+)加载的细胞内存储暴露于通透性VSMC中的低渗肿胀导致(45)Ca(2+)外排的增加,其被1 microM thapsigargin抑制,但不受50 microg / ml肝素的抑制, 50 microM钌红或25 microM thio-NADP。因此,VSMC的低渗肿胀会导致从细胞内存储区中释放一个Ca(2+),该区域是不同于IP(3)-,ryanodine-和烟酸腺嘌呤二核苷酸磷酸敏感存储区的一个新的站点。

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