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α-凝血酶和SFLLRN在大鼠胶质瘤C6细胞中的信号传导作用。

Signaling effects of alpha-thrombin and SFLLRN in rat glioma C6 cells.

作者信息

Kaufmann R, Lindschau C, Höer A, Henklein P, Adomeit A, Haller H, Liebmann C, Oberdisse E, Nowak G

机构信息

Max Planck Gesellschaft, Research Unit, Pharmacological Hemostaseology, Friedrich Schiller University Jena, Germany.

出版信息

J Neurosci Res. 1996 Dec 15;46(6):641-51. doi: 10.1002/(SICI)1097-4547(19961215)46:6<641::AID-JNR1>3.0.CO;2-F.

DOI:10.1002/(SICI)1097-4547(19961215)46:6<641::AID-JNR1>3.0.CO;2-F
PMID:8978498
Abstract

Effects of thrombin on brain cells, including change of neurite outgrowth and astrocyte shape, are described, but the molecular mechanisms are unclear. We investigated the effects of human alpha-thrombin and a six amino acid thrombin receptor activating peptide (TRAP-6, SFLLRN) on [Ca2+]i, phosphoinositide hydrolysis, and protein kinase C in rat glioma C6 cells. Stimulation of C6 cells with both alpha-thrombin and TRAP-6 resulted in [Ca2+]i mobilization, [3H]Inositol phosphate response, and enhanced immunoreactivity of the protein kinase C (PKC) isoenzymes alpha, beta, gamma, delta, and epsilon. Results suggest that alpha-thrombin and TRAP-6 activate at least partially the same intracellular signaling pathways in rat glioma C6 cells, which is evidence for involvement of "tethered ligand" receptor in thrombin induced signaling in glioma C6 cells.

摘要

文中描述了凝血酶对脑细胞的影响,包括神经突生长和星形胶质细胞形态的变化,但分子机制尚不清楚。我们研究了人α-凝血酶和一种六氨基酸凝血酶受体激活肽(TRAP-6,SFLLRN)对大鼠胶质瘤C6细胞中[Ca2+]i、磷酸肌醇水解和蛋白激酶C的影响。用α-凝血酶和TRAP-6刺激C6细胞均导致[Ca2+]i动员、[3H]肌醇磷酸反应,并增强了蛋白激酶C(PKC)同工酶α、β、γ、δ和ε的免疫反应性。结果表明,α-凝血酶和TRAP-6至少部分激活了大鼠胶质瘤C6细胞中相同的细胞内信号通路,这证明“拴系配体”受体参与了胶质瘤C6细胞中凝血酶诱导的信号传导。

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引用本文的文献

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Thrombin Activity and Thrombin Receptor in Rat Glioblastoma Model: Possible Markers and Targets for Intervention?大鼠胶质母细胞瘤模型中的凝血酶活性与凝血酶受体:可能的干预标志物和靶点?
J Mol Neurosci. 2015 Jul;56(3):644-51. doi: 10.1007/s12031-015-0512-y. Epub 2015 Feb 19.
2
Thrombin has a bimodal effect on glioma cell growth.凝血酶对胶质瘤细胞的生长具有双重作用。
Br J Cancer. 1997;76(12):1592-5. doi: 10.1038/bjc.1997.602.