Literature DB >> 2288702

Inositol phosphates in receptor-mediated cell signaling: metabolic origins and interrelationships.

C J Kirk1, S H Maccallum, R H Michell, C J Barker.   

Abstract

We have investigated the metabolic interrelationships of the major inositol phosphates in vasopressin-stimulated WRK 1 mammary tumor cells which were labeled to equilibrium with [14C]inositol and briefly, just prior to stimulation, with [3H]inositol. A comparison of the 3H/14C ratios of these compounds with those of the cellular inositol lipids suggests that most of the known inositol mono-, bis-, tris-, and tetrakis-phosphates are derived from precursors with turnover rates similar to those of these lipids. However, Ins(3,4,5,6)P4 (which is the major inositol tetrakisphosphate to accumulate in stimulated WRK 1 cells), Ins(1,3,4,5,6)P5, and InsP6 had 3H/14C ratios of 0 in this experiment, indicating that they must have a different metabolic origin.

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Year:  1990        PMID: 2288702

Source DB:  PubMed          Journal:  Biotechnol Appl Biochem        ISSN: 0885-4513            Impact factor:   2.431


  2 in total

1.  Thyroid-stimulating hormone rapidly stimulates inositol polyphosphate formation in FRTL-5 thyrocytes without activating phosphoinositidase C.

Authors:  J Singh; P Hunt; M C Eggo; M C Sheppard; C J Kirk; R H Michell
Journal:  Biochem J       Date:  1996-05-15       Impact factor: 3.857

2.  The interrelationships of the inositol phosphates formed in vasopressin-stimulated WRK-1 rat mammary tumour cells.

Authors:  C J Barker; N S Wong; S M Maccallum; P A Hunt; R H Michell; C J Kirk
Journal:  Biochem J       Date:  1992-09-01       Impact factor: 3.857

  2 in total

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