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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.

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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