PAR 1-type Thrombin Receptors are Involved in Thrombin-induced Calcium Signaling in Human Meningioma Cells

被引:0
|
作者
Roland Kaufmann
Stephan Patt
Robert Kraft
Michael Zieger
Peter Henklein
Gunter Neupert
Götz Nowak
机构
[1] Friedrich Schiller University Jena,Research Unit ‘Pharmacological Hemostaseology’
[2] Friedrich Schiller University Jena,Institute of Pathology (Neuropathology)
[3] Humboldt University,Institute of Biochemistry
来源
Journal of Neuro-Oncology | 1999年 / 42卷
关键词
proteinase-activated receptor 1; PAR 1; meningioma cells; thrombin; calcium signaling;
D O I
暂无
中图分类号
学科分类号
摘要
Thrombin is known to play a role as regulator in tumor spreading and tumor growth. Proteinase-activated receptor 1 (PAR 1)-type thrombin receptors were identified in different cancer cells including human glioblastoma cells. Thus a function of PAR 1 in brain tumors may be suggested. In this study, the presence of PAR 1-type thrombin receptors was investigated in primary cell cultures established from operated human meningiomas from two 59- and 79-year-old women. Characterization of PAR 1 on binding level was performed using immunofluorescence studies with the monoclonal anti-PAR 1 antibody Mab 61-1 directed against a domain in the NH2-terminus of PAR 1. These binding sites constitute functional thrombin receptors that are involved in thrombin-induced signaling in human meningioma cells as demonstrated by investigation of alpha-thrombin- and PAR 1-activating hexapeptide (TRAP-6)-induced [Ca2+]i mobilization. To our knowledge, this is the first report demonstrating thrombin-induced intracellular signaling in human meningioma cells mediated by the PAR 1-type thrombin receptor.
引用
收藏
页码:131 / 136
页数:5
相关论文
共 50 条
  • [31] Amyloid beta-peptide alters thrombin-induced calcium responses in cultured human neural cells
    Mattson, MP
    Begley, JG
    AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION, 1996, 3 (01): : 28 - 40
  • [32] Comparison of the effects of PAR1 antagonists, PAR4 antagonists, and their combinations on thrombin-induced human platelet activation
    Wu, Chin-Chung
    Teng, Che-Ming
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 546 (1-3) : 142 - 147
  • [33] Meizothrombin, an intermediate of prothrombin activation, stimulates human glioblastoma cells by interaction with PAR-1-type thrombin receptors
    Kaufmann, R
    Zieger, M
    Tausch, S
    Henklein, P
    Nowak, G
    JOURNAL OF NEUROSCIENCE RESEARCH, 2000, 59 (05) : 643 - 648
  • [34] Thrombin-induced Git1 phosphorylation in endothelial cells (ECs)
    Amerongen, GPV
    Hojo, Y
    Berk, BC
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (04) : 699 - 699
  • [35] PAR4 mediates thrombin-induced pro-coagulant activity in human platelets
    Lee, H.
    Berndt, C.
    Gardiner, E. E.
    Andrews, R. K.
    Jackson, S. P.
    Hamilton, J. R.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 : 70 - 70
  • [36] Diquertin suppresses ADP- and thrombin-induced accumulation of cytoplasmic calcium in human thrombocytes
    Kubatiev A.A.
    Yadigarova Z.T.
    Rud'ko I.A.
    Tyukavkina N.A.
    Bykov V.A.
    Pharmaceutical Chemistry Journal, 1999, 33 (12) : 629 - 630
  • [37] Adenosine opposes thrombin-induced inhibition of intercellular calcium wave in corneal endothelial cells
    D'hondt, Catheleyne
    Srinivas, Sangly P.
    Vereecke, Johan
    Himpens, Bernard
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2007, 48 (04) : 1518 - 1527
  • [38] SYNERGISTIC POTENTIATION BY EPINEPHRINE OF COLLAGEN OR THROMBIN-INDUCED CALCIUM MOBILIZATION IN HUMAN-PLATELETS
    ARDLIE, NG
    BELL, LK
    MCGUINESS, JA
    THROMBOSIS RESEARCH, 1987, 46 (04) : 519 - 526
  • [39] INHIBITORY EFFECT OF TRIMETAZIDINE ON THROMBIN-INDUCED AGGREGATION AND CALCIUM-ENTRY INTO HUMAN PLATELETS
    ASTARIEDEQUEKER, C
    JOULIN, Y
    DEVYNCK, MA
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1994, 23 (03) : 401 - 407
  • [40] CATHEPSIN-G AND THROMBIN-INDUCED ACTIVATION OF HUMAN ENDOTHELIAL-CELLS
    STORCK, J
    KARIMI, M
    BERTRAM, H
    ZIMMERMANN, RE
    THROMBOSIS AND HAEMOSTASIS, 1995, 73 (06) : 933 - 933