Multiple aspects of male germ cell development and interactions with Sertoli cells require inositol hexakisphosphate kinase-1
Autor: | Tomas Rojas, Alfred C. Chin, Chenglai Fu, Lauren K. Albacarys, Isaac A. Bernstein, William W. Wright, Solomon H. Snyder, Weiwei Cheng |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Male
0301 basic medicine Cell signaling endocrine system Science Cell Communication Biology Article Mice 03 medical and health sciences 0302 clinical medicine medicine Animals Spermatogenesis Infertility Male Phosphotransferases (Phosphate Group Acceptor) Sertoli Cells Multidisciplinary Inositol Hexakisphosphate Kinase 1 urogenital system Apical ectoplasmic specialization Epididymis Sertoli cell Spermatids Spermatozoa Sperm Cell biology Germ Cells 030104 developmental biology medicine.anatomical_structure Medicine Gene Deletion 030217 neurology & neurosurgery Germ cell |
Zdroj: | Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | Inositol hexakisphosphate kinase-1 (IP6K1) is required for male fertility, but the underlying mechanisms have been elusive. Here, we report that IP6K1 is required for multiple aspects of male germ cell development. This development requires selective interactions between germ cells and Sertoli cells, namely apical ectoplasmic specialization. Spermiation (sperm release) requires tubulobulbar complexes. We found that the apical ectoplasmic specialization and tubulobulbar complexes were poorly formed or disrupted in IP6K1 KOs. Deletion of IP6K1 elicited several aberrations, including: 1, sloughing off of round germ cells; 2, disorientation and malformation of elongating/elongated spermatids; 3, degeneration of acrosomes; 4, defects in germ-Sertoli cell interactions and 5, failure of spermiation. Eventually the sperm cells were not released but phagocytosed by Sertoli cells leading to an absence of sperm in the epididymis. |
Databáze: | OpenAIRE |
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