4.3 Article

Roles of cADPR and NAADP in pancreatic beta cell signaling

期刊

CELL CALCIUM
卷 103, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ceca.2022.102562

关键词

Ca2+ signaling; CD38; Cyclic ADP-ribose; NAADP; Ryanodine receptor; Endoplasmic reticulum; Pancreatic beta cell; Insulin; GLP-1

资金

  1. Korean National Research Foundation [2012R1A3A2026453]
  2. Wonkwang University
  3. National Research Foundation of Korea [2012R1A3A2026453] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this review, the roles of cADPR and NAADP in pancreatic beta cells are summarized, along with the intracellular Ca2+ stores and Ca2+ channels they target. Studying the roles of these signaling messengers helps us understand Ca2+ signaling and pathophysiology.
Since the discovery of the pyridine nucleotide metabolites Ca2+ mobilizing messengers cyclic ADP-ribose (cADPR) and nicotinic acid adenine dinucleotide phosphate (NAADP), they have been demonstrated to function as Ca2+ signaling messengers in a wide range of cell types. In this review, I will briefly summarize the roles of cADPR and NAADP in the physiological process of stimulus-secretion coupling in pancreatic beta cells. I am also going to outline the current breadth of knowledge regarding intracellular Ca2+ stores and Ca2+ channels targeted by cADPR and NAADP, as well as the biogenesis of these Ca2+ signaling messengers. I focused on receptor-mediated Ca2+ signaling in mediating the effects of GLP-1 and insulin in pancreatic beta cells. A better grasp in the roles of these signaling messengers will assist in our understanding of Ca2+ signaling as well as pathophysiology.

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