Literature DB >> 1657095

The nature and mechanism of activation of the hepatocyte receptor-activated Ca2+ inflow system.

G J Barritt1, B P Hughes.   

Abstract

Progress in elucidation of the properties of the hepatocyte receptor-activated Ca2+ inflow system (RACIS) has been hampered by difficulties in measuring rates of Ca2+ inflow to hepatocytes. These difficulties have led, for example, to different conclusions about the relationship between the extracellular Ca2+ concentration and the movement of Ca2+ through the RACIS. The hepatocyte RACIS admits Mn2+ and a number of other divalent cations as well as Ca2+. Many of these cations also inhibit the movement of Ca2+ through this system. While the RACIS is inhibited by high concentrations of verapamil and by some other Ca2+ antagonists, it is relatively insensitive to inhibition by organic compounds which inhibit other Ca2+ channels and Ca2+ transporters. There is circumstantial evidence which suggests that the hepatocyte RACIS is an exchange system, possibly one which catalyses Ca(2+)-H+ exchange or the co-transport of Ca2+ and OH-. Other circumstantial evidence suggests that the RACIS is a channel, with some similarities to voltage-operated Ca2+ channels in excitable cells. However, experiments using the patch-clamp technique have not yet detected agonist-stimulated Ca2+ movement across the hepatocyte plasma membrane. The molecular components of the RACIS probably differ from those which facilitate the large inflow of Ca2+ to hepatocytes which occurs in the absence of an agonist. The mechanism by which agonists activate the RACIS has not been elucidated.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1657095     DOI: 10.1016/0898-6568(91)90056-z

Source DB:  PubMed          Journal:  Cell Signal        ISSN: 0898-6568            Impact factor:   4.315


  9 in total

1.  Pinocytosis in 2,5-di-tert-butylhydroquinone-stimulated hepatocytes and evaluation of its role in Ca2+ inflow.

Authors:  K C Fernando; G J Barritt
Journal:  Mol Cell Biochem       Date:  1996-09-06       Impact factor: 3.396

2.  Histamine H1-receptor-mediated calcium influx in DDT1MF-2 cells.

Authors:  J M Dickenson; S J Hill
Journal:  Biochem J       Date:  1992-06-01       Impact factor: 3.857

3.  A role for protein kinase C-mediated phosphorylation in eliciting glucagon desensitization in rat hepatocytes.

Authors:  A Savage; L Zeng; M D Houslay
Journal:  Biochem J       Date:  1995-04-01       Impact factor: 3.857

4.  Suppression of agonist induced Ca2+ oscillations in cultured hepatocytes by nafenopin: possible involvement of protein kinase C.

Authors:  E Leibold; A Stampfl; L R Schwarz
Journal:  Arch Toxicol       Date:  1996       Impact factor: 5.153

5.  A slowly ADP-ribosylated pertussis-toxin-sensitive GTP-binding regulatory protein is required for vasopressin-stimulated Ca2+ inflow in hepatocytes.

Authors:  L A Berven; B P Hughes; G J Barritt
Journal:  Biochem J       Date:  1994-04-15       Impact factor: 3.857

6.  Extracellular calcium modulates insulin's action on enzymes controlling cyclic AMP metabolism in intact hepatocytes.

Authors:  F Irvine; A V Wallace; S R Sarawak; M D Houslay
Journal:  Biochem J       Date:  1993-07-01       Impact factor: 3.857

7.  Adenosine 5'-[alpha beta-methylene]triphosphate potentiates the oscillatory cytosolic Ca2+ responses of hepatocytes to ATP, but not to ADP.

Authors:  C J Dixon; P H Cobbold; A K Green
Journal:  Biochem J       Date:  1993-08-01       Impact factor: 3.857

Review 8.  Calcium: its modulation in liver by cross-talk between the actions of glucagon and calcium-mobilizing agonists.

Authors:  F L Bygrave; A Benedetti
Journal:  Biochem J       Date:  1993-11-15       Impact factor: 3.857

9.  Evidence from studies with hepatocyte suspensions that store-operated Ca2+ inflow requires a pertussis toxin-sensitive trimeric G-protein.

Authors:  K C Fernando; G J Barritt
Journal:  Biochem J       Date:  1994-10-15       Impact factor: 3.857

  9 in total

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