Literature DB >> 10617283

Maitotoxin-induced free Ca changes in single rat hepatocytes.

N M Woods1, C J Dixon, T Yasumoto, K S Cuthbertson, P H Cobbold.   

Abstract

We report the results using bioluminescent and fluorescent indicators to investigate maitotoxin-induced free Ca changes in single rat hepatocytes. Maitotoxin generated a steadily rising free Ca increase after a long lag period. The free Ca increase was dependent on extracellular calcium and could be antagonised by chelation of extracellular calcium or the inclusion of nickel in the superfusate. Manganese-induced quench of cytoplasmic Fura2 dextran revealed an accelerated rate of calcium entry during the final period of the lag phase, immediately prior to the free Ca increase. Imaging experiments demonstrated a markedly different part of free Ca mobilisation compared with glycogenolytic stimuli. Moreover, the use of a combination of hormonal stimuli and maitotoxin revealed that some cells could exhibit free Ca oscillations despite steadily rising intracellular free Ca level. The significance of these observations in terms of the mechanism of action of maitotoxin and the mechanism of free Ca transient generation is discussed.

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Year:  1999        PMID: 10617283     DOI: 10.1016/s0898-6568(99)00046-7

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


  5 in total

1.  Evidence that Ca2+-release-activated Ca2+ channels in rat hepatocytes are required for the maintenance of hormone-induced Ca2+ oscillations.

Authors:  Roland B Gregory; Gregory J Barritt
Journal:  Biochem J       Date:  2003-03-01       Impact factor: 3.857

2.  Maintenance of the filamentous actin cytoskeleton is necessary for the activation of store-operated Ca2+ channels, but not other types of plasma-membrane Ca2+ channels, in rat hepatocytes.

Authors:  Ying-Jie Wang; Roland B Gregory; Greg J Barritt
Journal:  Biochem J       Date:  2002-04-01       Impact factor: 3.857

3.  Evidence that 2-aminoethyl diphenylborate is a novel inhibitor of store-operated Ca2+ channels in liver cells, and acts through a mechanism which does not involve inositol trisphosphate receptors.

Authors:  R B Gregory; G Rychkov; G J Barritt
Journal:  Biochem J       Date:  2001-03-01       Impact factor: 3.857

4.  Evidence that TRPC1 (transient receptor potential canonical 1) forms a Ca(2+)-permeable channel linked to the regulation of cell volume in liver cells obtained using small interfering RNA targeted against TRPC1.

Authors:  Jinglong Chen; Greg J Barritt
Journal:  Biochem J       Date:  2003-07-15       Impact factor: 3.857

Review 5.  Recombinant aequorin and green fluorescent protein as valuable tools in the study of cell signalling.

Authors:  A Chiesa; E Rapizzi; V Tosello; P Pinton; M de Virgilio; K E Fogarty; R Rizzuto
Journal:  Biochem J       Date:  2001-04-01       Impact factor: 3.857

  5 in total

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