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Prüschenk, Sally ; Majer, Michael ; Schreiber, Rainer ; Schlossmann, Jens

IRAG2 Interacts with IP3-Receptor Types 1, 2, and 3 and Regulates Intracellular Ca2+ in Murine Pancreatic Acinar Cells

Prüschenk, Sally, Majer, Michael , Schreiber, Rainer und Schlossmann, Jens (2021) IRAG2 Interacts with IP3-Receptor Types 1, 2, and 3 and Regulates Intracellular Ca2+ in Murine Pancreatic Acinar Cells. International Journal of Molecular Sciences 22 (24), S. 13409.

Veröffentlichungsdatum dieses Volltextes: 05 Apr 2022 04:53
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.52039


Zusammenfassung

The inositol 1,4,5-triphosphate receptor-associated 2 (IRAG2) is also known as Jaw1 or lymphoid-restricted membrane protein (LRMP) and shares homology with the inositol 1,4,5-triphosphate receptor-associated cGMP kinase substrate 1 (IRAG1). IRAG1 interacts with inositol trisphosphate receptors (IP3 receptors /IP3R) via its coiled-coil domain and modulates Ca2+ release from intracellular stores. ...

The inositol 1,4,5-triphosphate receptor-associated 2 (IRAG2) is also known as Jaw1 or lymphoid-restricted membrane protein (LRMP) and shares homology with the inositol 1,4,5-triphosphate receptor-associated cGMP kinase substrate 1 (IRAG1). IRAG1 interacts with inositol trisphosphate receptors (IP3 receptors /IP3R) via its coiled-coil domain and modulates Ca2+ release from intracellular stores. Due to the homology of IRAG1 and IRAG2, especially in its coiled-coil domain, it is possible that IRAG2 has similar interaction partners like IRAG1 and that IRAG2 also modulates intracellular Ca2+ signaling. In our study, we localized IRAG2 in pancreatic acinar cells of the exocrine pancreas, and we investigated the interaction of IRAG2 with IP3 receptors and its impact on intracellular Ca2+ signaling and exocrine pancreatic function, like amylase secretion. We detected the interaction of IRAG2 with different subtypes of IP3R and altered Ca2+ release in pancreatic acinar cells from mice lacking IRAG2. IRAG2 deficiency decreased basal levels of intracellular Ca2+, suggesting that IRAG2 leads to activation of IP3R under unstimulated basal conditions. Moreover, we observed that loss of IRAG2 impacts the secretion of amylase. Our data, therefore, suggest that IRAG2 modulates intracellular Ca2+ signaling, which regulates exocrine pancreatic function.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftInternational Journal of Molecular Sciences
Verlag:MDPI
Ort der Veröffentlichung:BASEL
Band:22
Nummer des Zeitschriftenheftes oder des Kapitels:24
Seitenbereich:S. 13409
Datum14 Dezember 2021
InstitutionenBiologie und Vorklinische Medizin > Institut für Physiologie
Chemie und Pharmazie > Institut für Pharmazie > Lehrstuhl Pharmakologie und Toxikologie (Prof. Schlossmann, ehemals Prof. Seifert)
Identifikationsnummer
WertTyp
10.3390/ijms222413409DOI
Stichwörter / KeywordsINOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; IP3 RECEPTOR; ENDOPLASMIC-RETICULUM; CALCIUM; PROTEIN; RELEASE; PHOSPHORYLATION; EXPRESSION; SIGNALS; JAW1; Ca2+ signaling; IP3R; IRAG; IRAG1; IRAG2; Jaw1; LRMP; pancreas; pancreatic acinar cells
Dewey-Dezimal-Klassifikation500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 615 Pharmazie
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-520397
Dokumenten-ID52039

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