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Connexin 43 a check-point component of cell proliferation implicated in a wide range of human testis diseases
Authors:Daniel Chevallier  Diane Carette  Dominique Segretain  Jérome Gilleron  Georges Pointis
Affiliation:1. Department of Urology, Pasteur Hospital, Nice, France
2. INSERM U 1065, Team 5 “Physiopathologic Control of Germ Cell Proliferation: Genomic and Non Genomic Mechanisms”, University Nice Sophia-Antipolis, C3M, 151 route Saint-Antoine de Ginestière BP 2 3194, Nice Cedex 3, 06204, France
3. UMR S775, University Paris Descartes, 45 rue des Saints Pères, Paris, 75006, France
4. University of Versailles, Saint Quentin, 78035, France
5. Max Planck Institute of Molecular Cell Biology and Genetics, 01307, Dresden, Germany
Abstract:Gap junction channels link cytoplasms of adjacent cells. Connexins, their constitutive proteins, are essential in cell homeostasis and are implicated in numerous physiological processes. Spermatogenesis is a sophisticated model of germ cell proliferation, differentiation, survival, and apoptosis, in which a connexin isotype, connexin 43, plays a crucial role as evidenced by genomic approaches based on gene deletion. The balance between cell proliferation/differentiation/apoptosis is a prerequisite for maintaining levels of spermatozoa essential for fertility and for limiting anarchic cell proliferation, a major risk of testis tumor. The present review highlights the emerging role of connexins in testis pathogenesis, focusing specifically on two intimately interconnected human testicular diseases (azoospermia with impaired spermatogenesis and testicular germ cell tumors), whose incidence increased during the last decades. This work proposes connexin 43 as a potential cancer diagnostic and prognostic marker, as well as a promising therapeutic target for testicular diseases.
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