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机械损伤后细胞增殖需要局部伤口诱导的Ca2+信号与伤口前血清信号之间的协调。

Co-ordination between localized wound-induced Ca2+ signals and pre-wound serum signals is required for proliferation after mechanical injury.

作者信息

Tran P O, Tran Q H, Hinman L E, Sammak P J

机构信息

Pacific North-West Research Institute, Seattle, Washington, USA.

出版信息

Cell Prolif. 1998 Jun-Aug;31(3-4):155-70. doi: 10.1046/j.1365-2184.1998.00117.x.

Abstract

The signals which initiate proliferation of endothelial cells after injury are important for selective blood vessel growth during wound healing or tumour growth. Upon mechanically wounding quiescent cells, a transient [Ca2+]i increase was induced in cells at the wound edge. These same cells proliferated 18-24 h post wounding, as measured by bromodeoxyuridine incorporation. The localized Ca2+ signal was required specifically during wounding since blocking Ca2+ influx reduced proliferation by 40-50%. Proliferation also required serum since starvation reduced proliferation by 80%. Serum-starved cells proliferated if briefly primed with serum prior to wounding. The signals derived from serum and [Ca2+]i combined at least additively to induce proliferation. Therefore, serum priming followed by a single, transient Ca2+ signal induced by mechanical injury must occur in a temporally and spatially regulated manner for normal proliferation. Co-ordination between signalling cascades induced by growth factors and release from contact inhibition might be obligatory for localized re-endothelialization after injury.

摘要

损伤后启动内皮细胞增殖的信号对于伤口愈合或肿瘤生长过程中的选择性血管生长很重要。在对静止细胞进行机械损伤时,伤口边缘的细胞会诱导[Ca2+]i短暂升高。通过溴脱氧尿苷掺入法测量,这些相同的细胞在受伤后18 - 24小时开始增殖。局部Ca2+信号在受伤期间是特别需要的,因为阻断Ca2+内流会使增殖减少40 - 50%。增殖也需要血清,因为饥饿会使增殖减少80%。如果在受伤前用血清短暂预处理,血清饥饿的细胞会增殖。血清和[Ca2+]i产生的信号至少以相加的方式共同诱导增殖。因此,血清预处理后再由机械损伤诱导单一的短暂Ca2+信号,必须以时间和空间上受调控的方式发生才能实现正常增殖。生长因子诱导的信号级联与接触抑制释放之间的协调对于损伤后的局部再内皮化可能是必不可少的。

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本文引用的文献

1
Wound-induced calcium waves in alveolar type II cells.
Am J Physiol. 1997 Dec;273(6):L1242-8. doi: 10.1152/ajplung.1997.273.6.L1242.
3
How do injured cells communicate with the surviving cell monolayer?
J Cell Sci. 1997 Feb;110 ( Pt 4):465-75. doi: 10.1242/jcs.110.4.465.

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