Article (Scientific journals)
Specific deletion of AMP-activated protein kinase (α1AMPK) in mouse Sertoli cells modifies germ cell quality.
Bertoldo, Michael J; Guibert, Edith; Faure, Mélanie et al.
2016In Molecular and Cellular Endocrinology, 423, p. 96-112
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Keywords :
8L70Q75FXE (Adenosine Triphosphate); EC 2.7.11.31 (AMP-Activated Protein Kinases); EC 3.5.1.- (Sirt1 protein, mouse); EC 3.5.1.- (Sirtuin 1); AMP-Activated Protein Kinases/genetics/metabolism; Acrosome/enzymology; Adenosine Triphosphate/biosynthesis; Animals; Cell Proliferation; Cell Survival; Cells, Cultured; Female; Gene Expression; Infertility, Male/enzymology/genetics; Male; Mice, Inbred C57BL; Mice, Knockout; Protein Transport; Sertoli Cells/enzymology; Sirtuin 1/genetics/metabolism; Sperm Motility; AMP-activated protein kinase; Blood testis barrier; Fertility; Metabolism; Sertoli cells; Testis
Abstract :
[en] The AMP-activated protein kinase (AMPK) is an important regulator of cellular energy homeostasis which plays a role in fertility. Complete disruption of the AMPK catalytic subunit α1 gene (α1AMPK KO) in male mice results in a decrease in litter size which is associated with the production of altered sperm morphology and motility. Because of the importance of Sertoli cells in the formation of germ cells, we have chosen to selectively disrupt α1AMPK only in the Sertoli cells in mice (Sc-α1AMPK-KO mice). Specific deletion of the α1AMPK gene in Sertoli cells resulted in a 25% reduction in male fertility associated with abnormal spermatozoa with a thin head. No clear alterations in testis morphology or modification in the number of Sertoli cells in vivo were observed, but a dysregulation in energy metabolism in Sertoli cells occurred. We have reported an increase in lactate production, in lipid droplets, and a reduction in ATP production in Sc-α1AMPK-KO Sertoli cells. These perturbations were associated with lower expression of mitochondrial markers (cytochrome c and PGC1-α). In addition another metabolic sensor, the deacetylase SIRT1, had a reduction in expression which is correlated with a decline in deacetylase activity. Finally, expression and localization of junctions forming the blood-testis barrier between Sertoli cells themselves and with germ cells were deregulated in Sc-α1AMPK-KO. In conclusion, these results suggest that dysregulation of the energy sensing machinery exclusively through disruption of α1AMPK in Sertoli cells translates to a reduction in the quality of germ cells and fertility.
Disciplines :
Endocrinology, metabolism & nutrition
Author, co-author :
Bertoldo, Michael J;  Unité de Physiologie de la Reproduction et des Comportements, Institut National
Guibert, Edith;  Unité de Physiologie de la Reproduction et des Comportements, Institut National
Faure, Mélanie  ;  Université de Liège - ULiège > GIGA > GIGA Neurosciences - Neuroendocrinology ; Unité de Physiologie de la Reproduction et des Comportements, Institut National
Guillou, Florian;  Unité de Physiologie de la Reproduction et des Comportements, Institut National
Ramé, Christelle;  Unité de Physiologie de la Reproduction et des Comportements, Institut National
Nadal-Desbarats, Lydie;  INSERM U930, Équipe Neurogénétique et Neurométabolomique, Université
Foretz, Marc;  INSERM, U1016, Institut Cochin, Paris, France, CNRS, UMR8104, Paris, France, Univ
Viollet, Benoit;  INSERM, U1016, Institut Cochin, Paris, France, CNRS, UMR8104, Paris, France, Univ
Dupont, Joëlle;  Unité de Physiologie de la Reproduction et des Comportements, Institut National
Froment, Pascal;  Unité de Physiologie de la Reproduction et des Comportements, Institut National
Language :
English
Title :
Specific deletion of AMP-activated protein kinase (α1AMPK) in mouse Sertoli cells modifies germ cell quality.
Publication date :
05 March 2016
Journal title :
Molecular and Cellular Endocrinology
ISSN :
0303-7207
eISSN :
1872-8057
Publisher :
Elsevier, Nl
Volume :
423
Pages :
96-112
Peer reviewed :
Peer Reviewed verified by ORBi
Commentary :
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.
Available on ORBi :
since 19 January 2023

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