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活化血小板释放的新型内皮细胞活化因子,可诱导E选择素表达及肿瘤细胞与内皮细胞黏附:初步报告

Novel endothelial cell activation factor(s) released from activated platelets which induce E-selectin expression and tumor cell adhesion to endothelial cells: a preliminary note.

作者信息

Hakomori S

机构信息

Biomembrane Institute, Seattle, WA 98119.

出版信息

Biochem Biophys Res Commun. 1994 Sep 30;203(3):1605-13. doi: 10.1006/bbrc.1994.2370.

DOI:10.1006/bbrc.1994.2370
PMID:7524488
Abstract

Activation of endothelial cells (ECs) by tumor cells (TCs) to elicit expression of adhesion receptors such as selectins and intercellular adhesion molecules (ICAMs) has been considered to facilitate TC-EC adhesion, the initial step in TC metastasis. Studies reported here indicate that: (i) TC lines tested did not activate ECs; (ii) tested TCs activated native (but not inert) platelets, which in turn activated ECs to express E-selectin, leading to TC-EC adhesion; (iii) auto-aggregation of TCs eventually resulted in adhesion of large TC aggregates to ECs; (iv) process ii is inhibited by H7 and calphostin, indicating involvement of a signaling process mediated by protein kinases in expression of E-selectin.

摘要

肿瘤细胞(TCs)激活内皮细胞(ECs)以引发诸如选择素和细胞间粘附分子(ICAMs)等粘附受体的表达,这一过程被认为有助于TC-EC粘附,即TC转移的起始步骤。此处报道的研究表明:(i)所测试的TC系并未激活ECs;(ii)所测试的TCs激活天然(而非惰性)血小板,而血小板继而激活ECs以表达E-选择素,从而导致TC-EC粘附;(iii)TCs的自动聚集最终导致大的TC聚集体与ECs粘附;(iv)过程ii受到H7和钙泊三醇的抑制,表明蛋白激酶介导的信号传导过程参与了E-选择素的表达。

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