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Animal models of male subfertility targeted on LanCL1-regulated spermatogenic redox homeostasis / Chao Huang in LabAnimal, Vol.22 N°6 (juin 2022)

Public ISBD [article]  inLabAnimal > Vol.22 N°6 (juin 2022) . - p. 5-25 Titre : Animal models of male subfertility targeted on LanCL1-regulated spermatogenic redox homeostasis Type de document : texte imprimé Auteurs : Chao Huang ; Chengcheng Yang ; Dejiang Pang Année de publication : 2022 Article en page(s) : p. 5-25 Langues : Anglais (eng) Résumé : Oxidative stress in spermatozoa is a major contributor to male subfertility, which makes it an informed choice to generate animal models of male subfertility with targeted modifications of the antioxidant systems. However, the critical male germ cell-specific antioxidant mechanisms have not been well defined yet. Here we identify LanCL1 as a major male germ cell-specific antioxidant gene, reduced expression of which is related to human male infertility. Mice deficient in LanCL1 display spermatozoal oxidative damage and impaired male fertility. Histopathological studies reveal that LanCL1-mediated antioxidant response is required for mouse testicular homeostasis, from the initiation of spermatogenesis to the maintenance of viability and functionality of male germ cells. Conversely, a mouse model expressing LanCL1 transgene is protected against high-fat-diet/obesity-induced oxidative damage and subfertility. We further show that germ cell-expressed LanCL1, in response to spermatogenic reactive oxygen species, is regulated by transcription factor specific protein 1 (SP1) during spermatogenesis. This study demonstrates a critical role for the SP1–LanCL1 axis in regulating testicular homeostasis and male fertility mediated by redox balance, and provides evidence that LanCL1 genetically modified mice have attractive applications as animal models of male subfertility. Permalink : ./index.php?lvl=notice_display&id=104765 [article] Animal models of male subfertility targeted on LanCL1-regulated spermatogenic redox homeostasis [texte imprimé] / Chao Huang ; Chengcheng Yang ; Dejiang Pang . - 2022 . - p. 5-25. Langues : Anglais (eng) in LabAnimal > Vol.22 N°6 (juin 2022) . - p. 5-25 Résumé : Oxidative stress in spermatozoa is a major contributor to male subfertility, which makes it an informed choice to generate animal models of male subfertility with targeted modifications of the antioxidant systems. However, the critical male germ cell-specific antioxidant mechanisms have not been well defined yet. Here we identify LanCL1 as a major male germ cell-specific antioxidant gene, reduced expression of which is related to human male infertility. Mice deficient in LanCL1 display spermatozoal oxidative damage and impaired male fertility. Histopathological studies reveal that LanCL1-mediated antioxidant response is required for mouse testicular homeostasis, from the initiation of spermatogenesis to the maintenance of viability and functionality of male germ cells. Conversely, a mouse model expressing LanCL1 transgene is protected against high-fat-diet/obesity-induced oxidative damage and subfertility. We further show that germ cell-expressed LanCL1, in response to spermatogenic reactive oxygen species, is regulated by transcription factor specific protein 1 (SP1) during spermatogenesis. This study demonstrates a critical role for the SP1–LanCL1 axis in regulating testicular homeostasis and male fertility mediated by redox balance, and provides evidence that LanCL1 genetically modified mice have attractive applications as animal models of male subfertility. Permalink : ./index.php?lvl=notice_display&id=104765

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