Suppr超能文献

胶原蛋白对单个人类血小板胞质钙的调节作用

Regulation of cytosolic calcium by collagen in single human platelets.

作者信息

Poole A W, Watson S P

机构信息

University Department of Pharmacology, Oxford.

出版信息

Br J Pharmacol. 1995 May;115(1):101-6. doi: 10.1111/j.1476-5381.1995.tb16326.x.

Abstract
  1. There is controversy in the literature as to whether collagen is able to induce directly a rise in cytosolic calcium concentration ([Ca2+]i) in human platelets. We have addressed this question by observing the cytosolic calcium response of single fura-2-loaded human platelets settling onto a collagen-coated surface using dynamic fluorescence ratio imaging. 2. Following a short lag phase after adherence to collagen fibres, platelets underwent a rapid rise in cytosolic calcium from basal values of 80 +/- 13 nM (n = 24) to a peak of 475 +/- 42 nM (n = 24) which was sustained for the remaining period of the experiment. 3. The tyrphostin protein tyrosine kinase inhibitor, ST271, reduced substantially the proportion of platelets which exhibited a rise in [Ca2+]i on adherence to collagen and transformed the response in remaining cells to one of oscillations. 4. In contrast, and as a control for collagen, laminin-coated surfaces induced adherence of human platelets without elevating intracellular [Ca2+]; the cells however remained responsive to ADP. 5. We conclude that collagen directly induces a rise in cytosolic calcium in single human platelets through a tyrosine kinase-mediated pathway.
摘要
  1. 关于胶原蛋白是否能够直接诱导人血小板胞质钙浓度([Ca2+]i)升高,文献中存在争议。我们通过使用动态荧光比率成像观察单个负载fura-2的人血小板沉降到胶原蛋白包被表面后的胞质钙反应,来解决这个问题。2. 在黏附于胶原纤维后的短暂延迟期后,血小板胞质钙从基础值80±13 nM(n = 24)迅速升高至峰值475±42 nM(n = 24),并在实验剩余时间内保持该水平。3. 酪氨酸磷酸化蛋白酪氨酸激酶抑制剂ST271显著降低了黏附于胶原蛋白时表现出[Ca2+]i升高的血小板比例,并将剩余细胞的反应转变为振荡反应之一。4. 相比之下,作为胶原蛋白的对照,层粘连蛋白包被的表面诱导人血小板黏附,但不升高细胞内[Ca2+];然而,细胞对ADP仍有反应。5. 我们得出结论,胶原蛋白通过酪氨酸激酶介导的途径直接诱导单个正常人血小板胞质钙升高。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/100e/1908739/81bdfe9fd9a7/brjpharm00184-0111-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验