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Endocrine and paracrine calcium signaling in bile duct cells.

Bile duct cells play an important role in maintaining, modifying and augmenting bile flow. It is well established that cyclic AMP (cAMP) is an important second messenger for secretion in these cells, but less is known about cytosolic Ca2+ (Ca2+i). Here we review evidence that ATP and acetylcholine (...

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Detalles Bibliográficos
Autor principal: Nathanson, M. H.
Formato: Texto
Lenguaje:English
Publicado: Yale Journal of Biology and Medicine 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589330/
https://www.ncbi.nlm.nih.gov/pubmed/9626755
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author Nathanson, M. H.
author_facet Nathanson, M. H.
author_sort Nathanson, M. H.
collection PubMed
description Bile duct cells play an important role in maintaining, modifying and augmenting bile flow. It is well established that cyclic AMP (cAMP) is an important second messenger for secretion in these cells, but less is known about cytosolic Ca2+ (Ca2+i). Here we review evidence that ATP and acetylcholine (ACh) are Ca2+i agonists for bile duct cells, and that these agonists increase Ca2+i through inositol 1,4,5-trisphosphate (InsP3). We also review data suggesting that hepatocytes have the ability to secrete ATP, so that they may serve as a paracrine source for this signaling molecule in vivo. Finally, we compare the effects of cAMP and Ca2+i on secretion, both in isolated bile duct units and isolated hepatocyte couplets. Implications and future directions for studying the role of Ca2+i in bile ductular secretion are discussed.
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spelling pubmed-25893302008-12-01 Endocrine and paracrine calcium signaling in bile duct cells. Nathanson, M. H. Yale J Biol Med Research Article Bile duct cells play an important role in maintaining, modifying and augmenting bile flow. It is well established that cyclic AMP (cAMP) is an important second messenger for secretion in these cells, but less is known about cytosolic Ca2+ (Ca2+i). Here we review evidence that ATP and acetylcholine (ACh) are Ca2+i agonists for bile duct cells, and that these agonists increase Ca2+i through inositol 1,4,5-trisphosphate (InsP3). We also review data suggesting that hepatocytes have the ability to secrete ATP, so that they may serve as a paracrine source for this signaling molecule in vivo. Finally, we compare the effects of cAMP and Ca2+i on secretion, both in isolated bile duct units and isolated hepatocyte couplets. Implications and future directions for studying the role of Ca2+i in bile ductular secretion are discussed. Yale Journal of Biology and Medicine 1997 /pmc/articles/PMC2589330/ /pubmed/9626755 Text en
spellingShingle Research Article
Nathanson, M. H.
Endocrine and paracrine calcium signaling in bile duct cells.
title Endocrine and paracrine calcium signaling in bile duct cells.
title_full Endocrine and paracrine calcium signaling in bile duct cells.
title_fullStr Endocrine and paracrine calcium signaling in bile duct cells.
title_full_unstemmed Endocrine and paracrine calcium signaling in bile duct cells.
title_short Endocrine and paracrine calcium signaling in bile duct cells.
title_sort endocrine and paracrine calcium signaling in bile duct cells.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589330/
https://www.ncbi.nlm.nih.gov/pubmed/9626755
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