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The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium

Ovulation is an essential physiological process in sexual reproduction; however, the underlying cellular mechanisms are poorly understood. We have previously shown that OAMB, a Drosophila G-protein-coupled receptor for octopamine (the insect counterpart of mammalian norepinephrine), is required for...

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Autores principales: Lee, Hyun-Gwan, Rohila, Suman, Han, Kyung-An
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650798/
https://www.ncbi.nlm.nih.gov/pubmed/19262750
http://dx.doi.org/10.1371/journal.pone.0004716
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author Lee, Hyun-Gwan
Rohila, Suman
Han, Kyung-An
author_facet Lee, Hyun-Gwan
Rohila, Suman
Han, Kyung-An
author_sort Lee, Hyun-Gwan
collection PubMed
description Ovulation is an essential physiological process in sexual reproduction; however, the underlying cellular mechanisms are poorly understood. We have previously shown that OAMB, a Drosophila G-protein-coupled receptor for octopamine (the insect counterpart of mammalian norepinephrine), is required for ovulation induced upon mating. OAMB is expressed in the nervous and reproductive systems and has two isoforms (OAMB-AS and OAMB-K3) with distinct capacities to increase intracellular Ca(2+) or intracellular Ca(2+) and cAMP in vitro. Here, we investigated tissue specificity and intracellular signals required for OAMB's function in ovulation. Restricted OAMB expression in the adult oviduct epithelium, but not the nervous system, reinstated ovulation in oamb mutant females, in which either OAMB isoform was sufficient for the rescue. Consistently, strong immunoreactivities for both isoforms were observed in the wild-type oviduct epithelium. To delineate the cellular mechanism by which OAMB regulates ovulation, we explored protein kinases functionally interacting with OAMB by employing a new GAL4 driver with restricted expression in the oviduct epithelium. Conditional inhibition of Ca(2+)/Calmodulin-dependent protein kinase II (CaMKII), but not protein kinase A or C, in the oviduct epithelium inhibited ovulation. Moreover, constitutively active CaMKII, but not protein kinase A, expressed only in the adult oviduct epithelium fully rescued the oamb female's phenotype, demonstrating CaMKII as a major downstream molecule conveying the OAMB's ovulation signal. This is consistent with the ability of both OAMB isoforms, whose common intracellular signal in vitro is Ca(2+), to reinstate ovulation in oamb females. These observations reveal the critical roles of the oviduct epithelium and its cellular components OAMB and CaMKII in ovulation. It is conceivable that the OAMB-mediated cellular activities stimulated upon mating are crucial for secretory activities suitable for egg transfer from the ovary to the uterus.
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spelling pubmed-26507982009-03-05 The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium Lee, Hyun-Gwan Rohila, Suman Han, Kyung-An PLoS One Research Article Ovulation is an essential physiological process in sexual reproduction; however, the underlying cellular mechanisms are poorly understood. We have previously shown that OAMB, a Drosophila G-protein-coupled receptor for octopamine (the insect counterpart of mammalian norepinephrine), is required for ovulation induced upon mating. OAMB is expressed in the nervous and reproductive systems and has two isoforms (OAMB-AS and OAMB-K3) with distinct capacities to increase intracellular Ca(2+) or intracellular Ca(2+) and cAMP in vitro. Here, we investigated tissue specificity and intracellular signals required for OAMB's function in ovulation. Restricted OAMB expression in the adult oviduct epithelium, but not the nervous system, reinstated ovulation in oamb mutant females, in which either OAMB isoform was sufficient for the rescue. Consistently, strong immunoreactivities for both isoforms were observed in the wild-type oviduct epithelium. To delineate the cellular mechanism by which OAMB regulates ovulation, we explored protein kinases functionally interacting with OAMB by employing a new GAL4 driver with restricted expression in the oviduct epithelium. Conditional inhibition of Ca(2+)/Calmodulin-dependent protein kinase II (CaMKII), but not protein kinase A or C, in the oviduct epithelium inhibited ovulation. Moreover, constitutively active CaMKII, but not protein kinase A, expressed only in the adult oviduct epithelium fully rescued the oamb female's phenotype, demonstrating CaMKII as a major downstream molecule conveying the OAMB's ovulation signal. This is consistent with the ability of both OAMB isoforms, whose common intracellular signal in vitro is Ca(2+), to reinstate ovulation in oamb females. These observations reveal the critical roles of the oviduct epithelium and its cellular components OAMB and CaMKII in ovulation. It is conceivable that the OAMB-mediated cellular activities stimulated upon mating are crucial for secretory activities suitable for egg transfer from the ovary to the uterus. Public Library of Science 2009-03-05 /pmc/articles/PMC2650798/ /pubmed/19262750 http://dx.doi.org/10.1371/journal.pone.0004716 Text en Lee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lee, Hyun-Gwan
Rohila, Suman
Han, Kyung-An
The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium
title The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium
title_full The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium
title_fullStr The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium
title_full_unstemmed The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium
title_short The Octopamine Receptor OAMB Mediates Ovulation via Ca(2+)/Calmodulin-Dependent Protein Kinase II in the Drosophila Oviduct Epithelium
title_sort octopamine receptor oamb mediates ovulation via ca(2+)/calmodulin-dependent protein kinase ii in the drosophila oviduct epithelium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650798/
https://www.ncbi.nlm.nih.gov/pubmed/19262750
http://dx.doi.org/10.1371/journal.pone.0004716
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