Cannabinoid Receptor 1 Influences Chromatin Remodeling in Mouse Spermatids by Affecting Content of Transition Protein 2 mRNA and Histone Displacement

Author:

Chioccarelli Teresa1,Cacciola Giovanna1,Altucci Lucia2,Lewis Sheena E. M.3,Simon Luke3,Ricci Giulia4,Ledent Catherine5,Meccariello Rosaria6,Fasano Silvia17,Pierantoni Riccardo17,Cobellis Gilda17

Affiliation:

1. Dipartimento di Medicina Sperimentale (T.C., G.Ca., S.F., R.P., G.Co.), Sez. Bottazzi, Seconda Università di Napoli, 80138 Naples, Italy

2. Dipartimento di Patologia Generale (L.A.), Seconda Università degli Studi di Napoli, 80138 Naples, Italy

3. Centre for Public Health (S.E.M.L., L.S.), Institute of Clinical Science, Queen’s University Belfast, Belfast BT 12 6 BJ, Northern Ireland, United Kingdom

4. Dipartimento di Medicina Sperimentale (G.R.), Laboratorio di Istologia ed Embriologia, Seconda Università degli Studi di Napoli, 80138 Naples, Italy

5. Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (C.L.), Université Libre de Bruxelles, 1070 Brussels, Belgium

6. Dipartimento di Studi delle Istituzioni e dei Sistemi Territoriali (R.M.), Università degli Studi di Napoli Parthenope, 80133 Naples, Italy

7. Istituto Nazionale Biostrutture e Biosistemi (S.F., R.P., G.Co.), Consorzio Interuniversitario, Sezione di Napoli, 80138 Naples, Italy

Abstract

Marijuana smokers and animals treated with Δ9-tetrahydrocannabinol, the principal component of marijuana, show alterations of sperm morphology suggesting a role for cannabinoids in sperm differentiation and/or maturation. Because the cannabinoid receptor 1 (CNR1) activation appears to play a pivotal role in spermiogenesis, the developmental stage where DNA is remodeled, we hypothesized that CNR1 receptors might also influence chromatin quality in sperm. We used Cnr1 null mutant (Cnr1−/−) mice to study the possible role of endocannabinoids on sperm chromatin during spermiogenesis. We demonstrated that CNR1 activation regulated chromatin remodeling of spermatids by either increasing Tnp2 levels or enhancing histone displacement. Comparative analysis of wild-type, Cnr1+/−, and Cnr1−/− animals suggested the possible occurrence of haploinsufficiency for Tnp2 turnover control by CNR1, whereas histone displacement was disrupted to a lesser extent. Furthermore, flow cytometry analysis demonstrated that the genetic loss of Cnr1 decreased sperm chromatin quality and was associated with sperm DNA fragmentation. This damage increased during epididymal transit, from caput to cauda. Collectively, our results show that the expression/activity of CNR1 controls the physiological alterations of DNA packaging during spermiogenesis and epididymal transit. Given the deleterious effects of sperm DNA damage on male fertility, we suggest that the reproductive function of marijuana users may also be impaired by deregulation of the endogenous endocannabinoid system.

Publisher

The Endocrine Society

Subject

Endocrinology

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