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      Role of Major Endocannabinoid-Binding Receptors during Mouse Oocyte Maturation

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          Abstract

          Endocannabinoids are key-players of female fertility and potential biomarkers of reproductive dysfunctions. Here, we investigated localization and expression of cannabinoid receptor type-1 and -2 (CB 1R and CB 2R), G-protein coupled receptor 55 (GPR55), and transient receptor potential vanilloid type 1 channel (TRPV1) in mouse oocytes collected at different stages of in vivo meiotic maturation (germinal vesicle, GV; metaphase I, MI; metaphase II, MII) through qPCR, confocal imaging, and western blot. Despite the significant decrease in CB 1R, CB 2R, and GPR55 mRNAs occurring from GV to MII, CB 2R and GPR55 protein contents increased during the same period. At GV, only CB 1R was localized in oolemma, but it completely disappeared at MI. TRPV1 was always undetectable. When oocytes were in vitro matured with CB 1R and CB 2R but not GPR55 antagonists, a significant delay of GV breakdown occurred, sustained by elevated intraoocyte cAMP concentration. Although CBRs antagonists did not affect polar body I emission or chromosome alignment, GPR55 antagonist impaired in ~75% of oocytes the formation of normal-sized MI and MII spindles. These findings open a new avenue to interrogate oocyte pathophysiology and offer potentially new targets for the therapy of reproductive alterations.

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          Endocannabinoids and Their Pharmacological Actions.

          The endocannabinoid system consists of G protein-coupled cannabinoid CB(1) and CB(2) receptors, of endogenous compounds known as endocannabinoids that can target these receptors, of enzymes that catalyse endocannabinoid biosynthesis and metabolism, and of processes responsible for the cellular uptake of some endocannabinoids. This review presents in vitro evidence that most or all of the following 13 compounds are probably orthosteric endocannabinoids since they have all been detected in mammalian tissues in one or more investigation, and all been found to bind to cannabinoid receptors, probably to an orthosteric site: anandamide, 2-arachidonoylglycerol, noladin ether, dihomo-γ-linolenoylethanolamide, virodhamine, oleamide, docosahexaenoylethanolamide, eicosapentaenoylethanolamide, sphingosine, docosatetraenoylethanolamide, N-arachidonoyldopamine, N-oleoyldopamine and haemopressin. In addition, this review describes in vitro findings that suggest that the first eight of these compounds can activate CB(1) and sometimes also CB(2) receptors and that another two of these compounds are CB(1) receptor antagonists (sphingosine) or antagonists/inverse agonists (haemopressin). Evidence for the existence of at least three allosteric endocannabinoids is also presented. These endogenous compounds appear to target allosteric sites on cannabinoid receptors in vitro, either as negative allosteric modulators of the CB1 receptor (pepcan-12 and pregnenolone) or as positive allosteric modulators of this receptor (lipoxin A(4)) or of the CB(2) receptor (pepcan-12). Also discussed are current in vitro data that indicate the extent to which some established or putative orthosteric endocannabinoids seem to target non-cannabinoid receptors and ion channels, particularly at concentrations at which they have been found to interact with CB(1) or CB(2) receptors.
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            The epidermal growth factor network: role in oocyte growth, maturation and developmental competence

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              Meiotic spindle assembly and chromosome segregation in oocytes

              Centrosomes play a key role in organizing the microtubule spindle that separates chromosomes during mitosis. Bennabi et al. review how microtubule spindle formation and chromosomal segregation also occur in oocytes during cell division by meiosis despite the absence of centrosomes.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                12 June 2019
                June 2019
                : 20
                : 12
                : 2866
                Affiliations
                [1 ]Department of Life, Health and Environmental Sciences, University of L’Aquila, 67100 L’Aquila, Italy; gianna.rossi@ 123456univaq.it (G.R.); valentina.dinisio@ 123456graduate.univaq.it (V.D.N.)
                [2 ]Faculty of Veterinary Medicine, University of Teramo, 64100 Teramo, Italy; soddi@ 123456unite.it
                [3 ]European Center for Brain Research, Santa Lucia Foundation IRCCS, 00142 Rome, Italy; m.maccarrone@ 123456unicampus.it
                [4 ]Department of Medicine, Campus Bio-Medico University of Rome, 00128 Rome, Italy
                Author notes
                [* ]Correspondence: sandra.cecconi@ 123456univaq.it ; Tel./Fax: +39-0862-433-459
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-8435-7925
                https://orcid.org/0000-0002-3990-2963
                Article
                ijms-20-02866
                10.3390/ijms20122866
                6627642
                31212770
                e144f40c-4e42-421c-a29e-02aeca939f53
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 21 May 2019
                : 08 June 2019
                Categories
                Article

                Molecular biology
                endocannabinoids,receptors,signal transduction,meiosis,oocyte
                Molecular biology
                endocannabinoids, receptors, signal transduction, meiosis, oocyte

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