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小鼠胰腺β细胞中钙离子和鸟苷三磷酸依赖性胞吐作用涉及共同和不同的步骤。

Ca(2+)- and GTP-dependent exocytosis in mouse pancreatic beta-cells involves both common and distinct steps.

作者信息

Proks P, Eliasson L, Ammälä C, Rorsman P, Ashcroft F M

机构信息

University Laboratory of Physiology, Oxford, UK.

出版信息

J Physiol. 1996 Oct 1;496 ( Pt 1)(Pt 1):255-64. doi: 10.1113/jphysiol.1996.sp021682.

DOI:10.1113/jphysiol.1996.sp021682
PMID:8910213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1160841/
Abstract
  1. The effects of GTP and Ca2+ on secretion from single pancreatic beta-cells were studied using capacitance measurements as an indicator of exocytosis. 2. GTP or GTP gamma S produced a concentration-dependent increase in cell capacitance in the absence of intracellular calcium. There was no effect of cyclic AMP or BAPTA an GTP-induced secretion. 3. In the absence of GTP, the relationship between intracellular calcium concentration and the maximum rate of secretion was fitted by the Hill equation with a slope factor of 2.5 and half-maximal activation at 1.6 microM intracellular Ca2+. Similar values were obtained in the presence of GTP gamma S, suggesting GTP does not alter the sensitivity of the secretory machinery to Ca2+. 4. GDP beta S alone had no effect on cell capacitance but caused a dose-dependent inhibition of exocytosis induced by infusion of either GTP gamma S or Ca2+, suggesting both stimuli involve G-protein activation. GDP beta S was without effect on exocytosis evoked by depolarization-mediated Ca2+ entry. 5. The time course of exocytosis following rapid elevation of GTP gamma S by photolysis of a caged precursor was dependent on the intracellular Ca2+ and cyclic AMP concentrations. 6. Our results are interpreted in terms of a model in which the secretory pathways stimulated by Ca2+ and GTP contain both common and separate parts.
摘要
  1. 利用电容测量作为胞吐作用的指标,研究了GTP和Ca2+对单个胰腺β细胞分泌的影响。2. 在无细胞内钙的情况下,GTP或GTPγS使细胞电容呈浓度依赖性增加。环磷酸腺苷(cAMP)或BAPTA对GTP诱导的分泌无影响。3. 在无GTP的情况下,细胞内钙浓度与最大分泌速率之间的关系符合希尔方程,斜率因子为2.5,在细胞内Ca2+浓度为1.6微摩尔时达到半最大激活。在存在GTPγS的情况下也获得了类似的值,表明GTP不会改变分泌机制对Ca2+的敏感性。4. 单独的GDPβS对细胞电容无影响,但对由GTPγS或Ca2+注入诱导的胞吐作用有剂量依赖性抑制,表明这两种刺激都涉及G蛋白激活。GDPβS对去极化介导的Ca2+内流引起的胞吐作用无影响。5. 通过笼锁前体的光解快速升高GTPγS后胞吐作用的时间进程取决于细胞内Ca2+和环磷酸腺苷浓度。6. 我们的结果根据一个模型进行解释,在该模型中,由Ca2+和GTP刺激的分泌途径包含共同和独立的部分。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adb/1160841/e6ba9075acca/jphysiol00389-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adb/1160841/e6ba9075acca/jphysiol00389-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8adb/1160841/e6ba9075acca/jphysiol00389-0258-a.jpg

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Regulated exocytosis.调节性胞吐作用
在3T3-L1脂肪细胞中,冷却在一个Ca2+依赖步骤降低了cAMP刺激的胞吐作用和脂联素分泌。
PLoS One. 2015 Mar 20;10(3):e0119530. doi: 10.1371/journal.pone.0119530. eCollection 2015.
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J Physiol. 2014 Dec 1;592(23):5169-86. doi: 10.1113/jphysiol.2014.280388. Epub 2014 Sep 5.
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