Tyrosine Kinase-Mediated Activation of Cytosolic Calcium Oscillations and Phastic Myometrical Contractions
Tyrosine Kinase-Mediated Activation of Cytosolic Calcium Oscillations and Phastic Myometrical Contractions
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酪氨酸激酶介导的胞质钙振荡和肌力收缩的激活
DOI:
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发表时间:
1999
期刊:
影响因子:
--
通讯作者:
M. Phillippe
中科院分区:
文献类型:
--
作者:
J. Ascher‐Landsberg;T. Saunders;M. Phillippe
These studies sought to test the hypothesis that tyrosine kinase-stimulated phasic myometrical contractions are mediated by activation of the phosphatidylinositol (PI)-signaling pathway and the generation of cytosolic calcium oscillations. For these studies, uterine tissue was obtained from adult female Sprague-Dawley white rats during the proestrus/estrus phase of the cycle. In vivo contraction studies were performed using pervanadate (a tyrosine phosphatase inhibitor) with and without inhibitors of the PI-signaling pathway, including 2-nitro-4-carboxyphenyl-N,N-diphenylcarbamate (a phospholipase C inhibitor), thimerosal (an inositol-trisphosphate receptor/channel inhibitor), and Ruthenium red (a ryanodine receptor inhibitor), and with oxytocin or prostaglandin F2α (two classic uterotonic agonists). Cytosolic calcium studies were performed using Fura-2-loaded myometrial strips. During these studies, pervanadate was observed to produce cytosolid calcium oscillations and phasic contractions in myometrical tissue comparable to those produced in response to oxytocin and prostaglandin F2α. The pervandate-stimulated phasic contractions were significantly suppressed in response to inhibition of phospholipase C, the inositol-trisphosphate receptor, and the ryanodine receptor, thereby confirming the importance of the PI-signaling pathway during tyrosine kinase-associated myometrical activity. Further confirming the important and shared role for the PI-signaling pathway during pervanadate-stimulated myometrical contractions, no significant additive effects were observed when classic uterotonic agonists such as oxytocin or prostaglandin F2α were combined with pervanadate.
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影响因子:
9.8
作者:
Phillippe,M
通讯作者:
Phillippe,M
影响因子:
4.8
作者:
C. Ku;Ansha Qian;Yeshao Wen;Khursheed Anwer;Barbara M. Sanborn
通讯作者:
C. Ku;Ansha Qian;Yeshao Wen;Khursheed Anwer;Barbara M. Sanborn
DOI:
10.1006/bbrc.1997.6163
发表时间:
1997
期刊:
Biochemical and biophysical research communications.
影响因子:
--
作者:
Phillippe,M;Basa,A
通讯作者:
Basa,A
DOI:
10.1006/bbrc.1995.1769
发表时间:
1995
期刊:
Biochemical and biophysical research communications.
影响因子:
--
作者:
Phillippe,M
通讯作者:
Phillippe,M
影响因子:
9.8
作者:
Bieber,E;Stratman,T;Sanseverino,M;Sangueza,J;Phillippe,M
通讯作者:
Phillippe,M