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Sohlh1 功能丧失型雄性和雌性不育模型对小鼠的整体健康的影响超出了性腺功能障碍。

Sohlh1 loss of function male and female infertility model impacts overall health beyond gonadal dysfunction in mice†.

机构信息

Department of Pathology, University of California San Francisco, San Francisco, CA, USA.

Institute of Human Genetics, University of California San Francisco, San Francisco, CA, USA.

出版信息

Biol Reprod. 2023 Apr 11;108(4):619-628. doi: 10.1093/biolre/ioad008.

Abstract

Reproductive longevity is associated with health outcomes. Early menopause, loss of ovarian function, and male infertility are linked to shorter lifespan and increased adverse health outcomes. Here we examined the extragonadal effects of whole animal loss of spermatogenesis and oogenesis specific basic helix-loop-helix 1 (Sohlh1) gene in mice, a well-described mouse model of female and male infertility. Sohlh1 encodes a transcription factor that is primarily expressed in the male and female germline and regulates germline differentiation. The Sohlh1 knockout mouse model, just like human individuals with SOHLH1 loss of function, presents with hypergonadotropic hypogonadism and loss of ovarian function in females and impaired spermatogenesis in males, with a seemingly gonad restricted phenotype in both sexes. However, extragonadal phenotyping revealed that Sohlh1 deficiency leads to abnormal immune profiles in the blood and ovarian tissues of female animals, sex-specific alterations of metabolites, and behavior and cognition changes. Altogether, these results show that Sohlh1 deficiency impacts overall health in both male and female mice.

摘要

生殖寿命与健康结果有关。早发性绝经、卵巢功能丧失和男性不育与寿命缩短和不良健康结果增加有关。在这里,我们研究了整个动物失去生殖细胞发生和卵发生特异性碱性螺旋-环-螺旋 1 (Sohlh1) 基因的性腺外效应,这是一种描述良好的男性和女性不育的小鼠模型。Sohlh1 编码一种转录因子,主要在雄性和雌性生殖细胞中表达,并调节生殖细胞分化。Sohlh1 敲除小鼠模型与 SOHLH1 功能丧失的人类个体一样,表现为促性腺激素性性腺功能减退和女性卵巢功能丧失以及男性精子发生受损,在两性中均表现出明显的性腺受限表型。然而,性腺外表型分析显示,Sohlh1 缺乏会导致雌性动物血液和卵巢组织中的免疫谱异常、代谢物的性别特异性改变以及行为和认知变化。总之,这些结果表明,Sohlh1 缺乏会影响雄性和雌性小鼠的整体健康。

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