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Does the bone morphogenetic protein 7 inhibit oocyte maturation by autocrine/paracrine in mud crab?
- Source :
-
General and comparative endocrinology [Gen Comp Endocrinol] 2018 Sep 15; Vol. 266, pp. 119-125. Date of Electronic Publication: 2018 May 07. - Publication Year :
- 2018
-
Abstract
- A bone morphogenetic protein ligand (BMP7) and its two receptors (BMPRIB and BMPRII) were recently cloned and characterized in the mud crab, Scylla paramamosain. However specific functions of BMP7 and the mechanistic pathways regulating its function are largely unidentified. In the present study, we separated oocytes and follicle cells from the ovarian explants of S. paramamosain. Subsequent analysis using semi-quantitative PCR demonstrated that the mRNA of Sp-BMP7 was exclusively expressed in follicle cells while Sp-BMPRs were expressed in both oocytes and follicle cells. In vitro experiments further showed that the mRNA and protein levels of Cyclin B increased but Sp-BMP7 declined in 17α, 20β-Dihydroxyprogesterone (DHP)-induced oocytes. Furthermore, the inhibitory effects of Sp-BMP7 were not affected by the elimination of the contact/gap junction-mediated communication between oocytes and follicle cells. Our data indicate that BMP7 may play a role in the suppression of DHP-induced oocyte maturation by affecting autocrine/paracrine pathways in S. paramamosain.<br /> (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Subjects :
- Algestone pharmacology
Animals
Bone Morphogenetic Protein Receptors, Type I metabolism
Bone Morphogenetic Protein Receptors, Type II metabolism
Brachyura drug effects
Cyclin B metabolism
Female
Oocytes drug effects
Oocytes metabolism
Oogenesis drug effects
Ovarian Follicle cytology
Ovarian Follicle drug effects
Ovarian Follicle metabolism
RNA Interference
RNA, Messenger genetics
Autocrine Communication drug effects
Bone Morphogenetic Protein 7 pharmacology
Brachyura cytology
Brachyura metabolism
Oocytes cytology
Paracrine Communication drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1095-6840
- Volume :
- 266
- Database :
- MEDLINE
- Journal :
- General and comparative endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 29746856
- Full Text :
- https://doi.org/10.1016/j.ygcen.2018.05.004