Tsuchida Kunihiro, Nakatani Masashi, Yamakawa Norio, Hashimoto Osamu, Hasegawa Yoshihisa, Sugino Hiromu
Institute for Enzyme Research, University of Tokushima, 3-18-15 Kuramoto, Tokushima 770-8503, Japan.
Mol Cell Endocrinol. 2004 May 31;220(1-2):59-65. doi: 10.1016/j.mce.2004.03.009.
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 beta 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.
激活素在细胞分化和发育中起重要作用。激活素A信号传导是通过激活素II型受体(ActRIIs)和激活素IB型受体ALK4共同介导的。其他激活素亚型的信号受体仍有待阐明。在此,我们发现激活素AB和激活素B是ALK7的配体。ALK7是一种孤儿受体丝氨酸/苏氨酸激酶,在包括胰岛在内的神经内分泌组织中表达。激活素AB和激活素B而非激活素A所偏好的ActRIIA与ALK7的组合,负责激活素介导的胰岛素从胰腺β细胞系MIN6中的分泌。相比之下,所有激活素均以不同程度的效力激活ActRIIA和ALK4的组合。因此,激活素通过I型受体的信号传导差异取决于激活素亚型的同二聚体和异二聚体组装。因此,受体异二聚体的不同组合介导了激活素亚型信号传导的差异。