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...

Full description

Saved in:
Bibliographic Details
Published inBiochemical and biophysical research communications Vol. 181; no. 3; pp. 997 - 1003
Main Authors Donié, Frédéric, Reiser, Georg
Format Journal Article
LanguageEnglish
Published San Diego, CA Elsevier Inc 31.12.1991
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
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.
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