Functional characterization of an invertebrate gonadotropin-releasing hormone receptor in the Yesso scallop Mizuhopecten yessoensis

被引:7
|
作者
Nagasawa, Kazue [1 ]
Matsubara, Shin [2 ]
Satake, Honoo [2 ]
Osada, Makoto [1 ]
机构
[1] Tohoku Univ, Grad Sch Agr Sci, Lab Aquacultural Biol, Aoba Ku, 468-1 Aoba, Sendai, Miyagi, Japan
[2] Suntory Fdn Life Sci, Bioorgan Res Inst, Kyoto, Japan
基金
日本学术振兴会;
关键词
Mollusc; Receptor assay; Second messenger; AKH; CFtZ; ACP; GnRH; GNRH; OCTOPUS; PEPTIDES; ENDOCRINE; SYSTEM;
D O I
10.1016/j.ygcen.2019.06.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The neuropeptide control of bivalve reproduction with particular reference to gonadotropin-releasing hormone (invGnRH) is a frontier yet to be investigated. Bivalves are unique because they have two forms of the invGnRH peptide; however, there has been no functional characterization of the peptide receptor pair. Therefore, the identification of a cognate receptor is a preliminary step toward exploring the biological roles of invGnRHs in bivalves. In this study, we functionally characterize an invGnRH receptor (invGnRHR) of a bivalve, the Yesso scallop Mizuhopecten yessoensis. In the receptor assay, HEK293 cells were transfected to transiently express the M. yessoensis invGnRHR (my-invGnRHR), which was found to be localized on the plasma membrane, confirming that my-invGnRHR, similar to other G-protein-coupled receptors, functions as a membrane receptor. Using both forms of invGnRH as ligands in a function-receptor assay, my-invGnRH11aa-NH2 stimulated intracellular Ca2+ mobilization but not cyclic AMP production, whereas my-invGnRH12aa-OH did not induce increase in Ca2+ levels. Therefore, we concluded that my-invGnRHR is an endogenous receptor specific to my-invGnRH11aa-NH2 which is hypothesized to be the mature peptide. To the best of our knowledge, this is the first study reporting the functional characterization of a bivalve invGnRHR.
引用
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页数:6
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