TY - JOUR
T1 - Activin isoforms signal through type I receptor serine/threonine kinase ALK7
AU - Tsuchida, Kunihiro
AU - Nakatani, Masashi
AU - Yamakawa, Norio
AU - Hashimoto, Osamu
AU - Hasegawa, Yoshihisa
AU - Sugino, Hiromu
N1 - Funding Information:
We thank Dr. C.-H. Heldin for providing the reporter plasmids and Dr. J. Miyazaki for the mouse pancreatic β cells. This research was supported by the Ministry of Education, Science, Sports, Culture and Technology of Japan and also supported by grants from The Yamanouchi Foundation for Research on Metabolic Disorders, The Fujisawa Foundation, and Kyowa Hakko Kogyo Co. Ltd. to K.T.
PY - 2004/5/31
Y1 - 2004/5/31
N2 - Activins play a fundamental role in cell differentiation and development. Activin A signaling is mediated through a combination of activin type II receptors (ActRIIs) and the activin type IB receptor, ALK4. Signaling receptors of other activin isoforms remain to be elucidated. Here, we found that activin AB and activin B are ligands for ALK7. ALK7 is an orphan receptor serine/threonine kinase expressed in neuroendocrine tissues including pancreatic islets. The combination of ActRIIA and ALK7, preferred by activin AB and activin B but not by activin A, is responsible for activin-mediated secretion of insulin from pancreatic β cell line, MIN6. In contrast, all activins activate a combination of ActRIIA and ALK4 with various levels of potency. Thus, variation in activin signaling through type I receptors is dependent upon homo- and heterodimeric assembly of activin isoforms. Thus, the differential combination of receptor heterodimers mediates variation in activin isoform signaling.
AB - Activins play a fundamental role in cell differentiation and development. Activin A signaling is mediated through a combination of activin type II receptors (ActRIIs) and the activin type IB receptor, ALK4. Signaling receptors of other activin isoforms remain to be elucidated. Here, we found that activin AB and activin B are ligands for ALK7. ALK7 is an orphan receptor serine/threonine kinase expressed in neuroendocrine tissues including pancreatic islets. The combination of ActRIIA and ALK7, preferred by activin AB and activin B but not by activin A, is responsible for activin-mediated secretion of insulin from pancreatic β cell line, MIN6. In contrast, all activins activate a combination of ActRIIA and ALK4 with various levels of potency. Thus, variation in activin signaling through type I receptors is dependent upon homo- and heterodimeric assembly of activin isoforms. Thus, the differential combination of receptor heterodimers mediates variation in activin isoform signaling.
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U2 - 10.1016/j.mce.2004.03.009
DO - 10.1016/j.mce.2004.03.009
M3 - Article
C2 - 15196700
AN - SCOPUS:2942527675
SN - 0303-7207
VL - 220
SP - 59
EP - 65
JO - Molecular and Cellular Endocrinology
JF - Molecular and Cellular Endocrinology
IS - 1-2
ER -