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Specific deletion of AMP-activated protein kinase (α1AMPK) in mouse Sertoli cells modifies germ cell quality.

Identifieur interne : 001722 ( Main/Exploration ); précédent : 001721; suivant : 001723

Specific deletion of AMP-activated protein kinase (α1AMPK) in mouse Sertoli cells modifies germ cell quality.

Auteurs : Michael J. Bertoldo [Australie] ; Edith Guibert [France] ; Melanie Faure [France] ; Florian Guillou [France] ; Christelle Ramé [France] ; Lydie Nadal-Desbarats [France] ; Marc Foretz [France] ; Benoit Viollet [France] ; Joëlle Dupont [France] ; Pascal Froment [France]

Source :

RBID : pubmed:26772142

Descripteurs français

English descriptors

Abstract

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.

DOI: 10.1016/j.mce.2016.01.001
PubMed: 26772142


Affiliations:


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Le document en format XML

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<term>AMP-Activated Protein Kinases (genetics)</term>
<term>AMP-Activated Protein Kinases (metabolism)</term>
<term>Acrosome (enzymology)</term>
<term>Adenosine Triphosphate (biosynthesis)</term>
<term>Animals</term>
<term>Cell Proliferation</term>
<term>Cell Survival</term>
<term>Cells, Cultured</term>
<term>Female</term>
<term>Gene Expression</term>
<term>Infertility, Male (enzymology)</term>
<term>Infertility, Male (genetics)</term>
<term>Male</term>
<term>Mice, Inbred C57BL</term>
<term>Mice, Knockout</term>
<term>Protein Transport</term>
<term>Sertoli Cells (enzymology)</term>
<term>Sirtuin 1 (genetics)</term>
<term>Sirtuin 1 (metabolism)</term>
<term>Sperm Motility</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>AMP-Activated Protein Kinases (génétique)</term>
<term>AMP-Activated Protein Kinases (métabolisme)</term>
<term>Acrosome (enzymologie)</term>
<term>Adénosine triphosphate (biosynthèse)</term>
<term>Animaux</term>
<term>Cellules cultivées</term>
<term>Cellules de Sertoli (enzymologie)</term>
<term>Expression des gènes</term>
<term>Femelle</term>
<term>Infertilité masculine (enzymologie)</term>
<term>Infertilité masculine (génétique)</term>
<term>Motilité des spermatozoïdes</term>
<term>Mâle</term>
<term>Prolifération cellulaire</term>
<term>Sirtuine-1 (génétique)</term>
<term>Sirtuine-1 (métabolisme)</term>
<term>Souris de lignée C57BL</term>
<term>Souris knockout</term>
<term>Survie cellulaire</term>
<term>Transport de protéines</term>
</keywords>
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<term>Adenosine Triphosphate</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>AMP-Activated Protein Kinases</term>
<term>Sirtuin 1</term>
</keywords>
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<term>AMP-Activated Protein Kinases</term>
<term>Sirtuin 1</term>
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<term>Adénosine triphosphate</term>
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<term>Acrosome</term>
<term>Cellules de Sertoli</term>
<term>Infertilité masculine</term>
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<term>Acrosome</term>
<term>Infertility, Male</term>
<term>Sertoli Cells</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Infertility, Male</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>AMP-Activated Protein Kinases</term>
<term>Infertilité masculine</term>
<term>Sirtuine-1</term>
</keywords>
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<term>AMP-Activated Protein Kinases</term>
<term>Sirtuine-1</term>
</keywords>
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<term>Animals</term>
<term>Cell Proliferation</term>
<term>Cell Survival</term>
<term>Cells, Cultured</term>
<term>Female</term>
<term>Gene Expression</term>
<term>Male</term>
<term>Mice, Inbred C57BL</term>
<term>Mice, Knockout</term>
<term>Protein Transport</term>
<term>Sperm Motility</term>
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<term>Animaux</term>
<term>Cellules cultivées</term>
<term>Expression des gènes</term>
<term>Femelle</term>
<term>Motilité des spermatozoïdes</term>
<term>Mâle</term>
<term>Prolifération cellulaire</term>
<term>Souris de lignée C57BL</term>
<term>Souris knockout</term>
<term>Survie cellulaire</term>
<term>Transport de protéines</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="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.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>France</li>
</country>
<region>
<li>Centre-Val de Loire</li>
<li>Région Centre</li>
<li>Île-de-France</li>
</region>
<settlement>
<li>Paris</li>
<li>Tours</li>
</settlement>
</list>
<tree>
<country name="Australie">
<noRegion>
<name sortKey="Bertoldo, Michael J" sort="Bertoldo, Michael J" uniqKey="Bertoldo M" first="Michael J" last="Bertoldo">Michael J. Bertoldo</name>
</noRegion>
</country>
<country name="France">
<noRegion>
<name sortKey="Guibert, Edith" sort="Guibert, Edith" uniqKey="Guibert E" first="Edith" last="Guibert">Edith Guibert</name>
</noRegion>
<name sortKey="Dupont, Joelle" sort="Dupont, Joelle" uniqKey="Dupont J" first="Joëlle" last="Dupont">Joëlle Dupont</name>
<name sortKey="Faure, Melanie" sort="Faure, Melanie" uniqKey="Faure M" first="Melanie" last="Faure">Melanie Faure</name>
<name sortKey="Foretz, Marc" sort="Foretz, Marc" uniqKey="Foretz M" first="Marc" last="Foretz">Marc Foretz</name>
<name sortKey="Froment, Pascal" sort="Froment, Pascal" uniqKey="Froment P" first="Pascal" last="Froment">Pascal Froment</name>
<name sortKey="Guillou, Florian" sort="Guillou, Florian" uniqKey="Guillou F" first="Florian" last="Guillou">Florian Guillou</name>
<name sortKey="Nadal Desbarats, Lydie" sort="Nadal Desbarats, Lydie" uniqKey="Nadal Desbarats L" first="Lydie" last="Nadal-Desbarats">Lydie Nadal-Desbarats</name>
<name sortKey="Rame, Christelle" sort="Rame, Christelle" uniqKey="Rame C" first="Christelle" last="Ramé">Christelle Ramé</name>
<name sortKey="Viollet, Benoit" sort="Viollet, Benoit" uniqKey="Viollet B" first="Benoit" last="Viollet">Benoit Viollet</name>
</country>
</tree>
</affiliations>
</record>

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