TY - JOUR
T1 - IRBIT
T2 - A regulator of ion channels and ion transporters
AU - Ando, Hideaki
AU - Kawaai, Katsuhiro
AU - Mikoshiba, Katsuhiko
N1 - Funding Information:
This work was supported by the Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research 23500458 (to H.A.), 24700389 (to K.K.) and 20220007 (to K.M.).
PY - 2014/10
Y1 - 2014/10
N2 - IRBIT (also called AHCYL1) was originally identified as a binding protein of the intracellular Ca2+ channel inositol 1,4,5-trisphosphate (IP3) receptor and functions as an inhibitory regulator of this receptor. Unexpectedly, many functions have subsequently been identified for IRBIT including the activation of multiple ion channels and ion transporters, such as the Na+/HCO3- co-transporter NBCe1-B, the Na+/H+ exchanger NHE3, the Cl- channel cystic fibrosis transmembrane conductance regulator (CFTR), and the Cl-/HCO3- exchanger Slc26a6. The characteristic serine-rich region in IRBIT plays a critical role in the functions of this protein. In this review, we describe the evolution, domain structure, expression pattern, and physiological roles of IRBIT and discuss the potential molecular mechanisms underlying the coordinated regulation of these diverse ion channels/transporters through IRBIT. This article is part of a Special Issue entitled: Calcium signaling in health and disease. Guest Editors: Geert Bultynck, Jacques Haiech, Claus W. Heizmann, Joachim Krebs, and Marc Moreau.
AB - IRBIT (also called AHCYL1) was originally identified as a binding protein of the intracellular Ca2+ channel inositol 1,4,5-trisphosphate (IP3) receptor and functions as an inhibitory regulator of this receptor. Unexpectedly, many functions have subsequently been identified for IRBIT including the activation of multiple ion channels and ion transporters, such as the Na+/HCO3- co-transporter NBCe1-B, the Na+/H+ exchanger NHE3, the Cl- channel cystic fibrosis transmembrane conductance regulator (CFTR), and the Cl-/HCO3- exchanger Slc26a6. The characteristic serine-rich region in IRBIT plays a critical role in the functions of this protein. In this review, we describe the evolution, domain structure, expression pattern, and physiological roles of IRBIT and discuss the potential molecular mechanisms underlying the coordinated regulation of these diverse ion channels/transporters through IRBIT. This article is part of a Special Issue entitled: Calcium signaling in health and disease. Guest Editors: Geert Bultynck, Jacques Haiech, Claus W. Heizmann, Joachim Krebs, and Marc Moreau.
KW - IP3 receptor
KW - IRBIT
UR - http://www.scopus.com/inward/record.url?scp=84904963138&partnerID=8YFLogxK
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U2 - 10.1016/j.bbamcr.2014.01.031
DO - 10.1016/j.bbamcr.2014.01.031
M3 - Review article
C2 - 24518248
AN - SCOPUS:84904963138
SN - 0167-4889
VL - 1843
SP - 2195
EP - 2204
JO - Biochimica et Biophysica Acta - Molecular Cell Research
JF - Biochimica et Biophysica Acta - Molecular Cell Research
IS - 10
ER -