Mass measurements of inositol 1,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate in a neuronal cell line stimulated with bradykinin: Inositolphosphate response shows desensitization
In a neuronal cell line (108CC15, NG108-15) the levels of inositol 1,4,5-trisphosphate (InsP 3) and inositol 1,3,4,5-tetrakisphosphate (InsP 4), as measured by receptor binding assays, rise transiently after stimulation with bradykinin (EC 50 approx. 150 nM). Maximal InsP 3 level 354 pmol/mg protein...
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Published in | Biochemical and biophysical research communications Vol. 181; no. 3; pp. 997 - 1003 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier Inc
31.12.1991
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | In a neuronal cell line (108CC15, NG108-15) the levels of inositol 1,4,5-trisphosphate (InsP
3) and inositol 1,3,4,5-tetrakisphosphate (InsP
4), as measured by receptor binding assays, rise transiently after stimulation with bradykinin (EC
50 approx. 150 nM). Maximal InsP
3 level 354 pmol/mg protein (15-fold basal level) is obtained at 10 – 15 s after addition of bradykinin, the InsP
4 level rises maximally to 78 pmol/mg protein (14-fold basal level) at 20 – 30 s. In a rat glioma cell line, bradykinin (2 μM) causes a fast 6-fold increase in InsP
3 and InsP
4 levels. In the neuronal cells the bradykinin-dependent rise of the inositolphosphate levels is diminished with reduced extracellular Ca
2+ concentration. However, depletion of internal Ca
2+ stores does not affect the bradykinin-induced rise in InsP
3 and InsP
4 levels. Homologous desensitization to bradykinin occurs in the signal transduction pathway already at the production of inositolphosphates, since after a 2 min stimulation with bradykinin the rise in cellular masses of InsP
3 and InsP
4, inducible by a following second bradykinin stimulus,is substantially reduced. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/0006-291X(91)92035-I |