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日本猕猴(Macaca fuscata)精子发生的分子组织学。

Molecular histology of spermatogenesis in the Japanese macaque monkey (Macaca fuscata).

机构信息

Molecular Biology Section, Department of Cellular and Molecular Biology, Primate Research Institute, Kyoto University, Inuyama, Aichi, 484-8506, Japan.

Department of Anthropology, Kent State University, Kent, Ohio, USA.

出版信息

Primates. 2021 Jan;62(1):113-121. doi: 10.1007/s10329-020-00857-8. Epub 2020 Aug 17.

DOI:10.1007/s10329-020-00857-8
PMID:32803510
Abstract

Non-human primates are our closest relatives and therefore offer valuable comparative models for human evolutionary studies and biomedical research. As such, Japanese macaques (Macaca fuscata) have contributed to the advancement of primatology in both field and laboratory settings. Specifically, Japanese macaques serve as an excellent model for investigating postnatal development and seasonal breeding in primates because of their relatively prolonged juvenile period and distinct seasonal breeding activity in adulthood. Pioneering histological studies have examined the developmental associations between their reproductive states and spermatogenesis by morphological observation. However, a molecular histological atlas of Japanese macaque spermatogenesis is only in its infancy, limiting our understanding of spermatogenesis ontogeny related to their reproductive changes. Here, we performed immunofluorescence analyses of spermatogenesis in Japanese macaque testes to determine the expression of a subset of marker proteins. The present molecular histological analyses readily specified major spermatogonial subtypes as SALL4 A spermatogonia and Ki67/C-KIT B spermatogonia. The expression of DAZL, SCP1, γH2AX, VASA, and calmegin further showed sequential changes regarding the protein expression profile and chromosomal structures during spermatogenesis in a differentiation stage-specific manner. Accordingly, comparative analyses between subadults and adults identified spermatogenic deficits in differentiation and synchronization in subadult testes. Our findings provide a new diagnostic platform for dissecting spermatogenic status and reproduction in the Japanese macaques.

摘要

非人类灵长类动物是我们最亲近的亲属,因此为人类进化研究和生物医学研究提供了有价值的比较模型。作为这样的模型,日本猕猴(Macaca fuscata)在野外和实验室环境中都为灵长类学的发展做出了贡献。具体来说,由于日本猕猴幼体期相对较长,成年后具有明显的季节性繁殖活动,因此它们是研究灵长类动物产后发育和季节性繁殖的极佳模型。开创性的组织学研究通过形态观察检查了它们的生殖状态和精子发生之间的发育关联。然而,日本猕猴精子发生的分子组织学图谱仍处于起步阶段,限制了我们对与生殖变化相关的精子发生个体发生的理解。在这里,我们对日本猕猴睾丸中的精子发生进行了免疫荧光分析,以确定一组标记蛋白的表达。目前的分子组织学分析很容易将主要精原细胞亚型鉴定为 SALL4A 精原细胞和 Ki67/C-KITB 精原细胞。DAZL、SCP1、γH2AX、VASA 和 calmegin 的表达进一步显示,在精子发生过程中,蛋白表达谱和染色体结构按分化阶段特异性发生顺序变化。因此,亚成体和成年个体之间的比较分析确定了亚成体睾丸中分化和同步的精子发生缺陷。我们的发现为剖析日本猕猴的精子发生状态和生殖提供了新的诊断平台。

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本文引用的文献

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Primate Biol. 2017 Sep 22;4(2):173-184. doi: 10.5194/pb-4-173-2017. eCollection 2017.
2
What has single-cell RNA-seq taught us about mammalian spermatogenesis?单细胞 RNA 测序让我们对哺乳动物精子发生有了哪些了解?
Biol Reprod. 2019 Sep 1;101(3):617-634. doi: 10.1093/biolre/ioz088.
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Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata).诱导性多能干细胞在日本猕猴(Macaca fuscata)中的衍生。
Sci Rep. 2018 Aug 15;8(1):12187. doi: 10.1038/s41598-018-30734-w.
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Spermatogonial stem cells and spermatogenesis in mice, monkeys and men.小鼠、猴子和人类的精原干细胞与精子发生
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Cumulative culture in nonhumans: overlooked findings from Japanese monkeys?非人类的累积文化:日本猕猴被忽视的发现?
Primates. 2018 Mar;59(2):113-122. doi: 10.1007/s10329-017-0642-7. Epub 2017 Dec 27.
6
The testicular transcriptome associated with spermatogonia differentiation initiated by gonadotrophin stimulation in the juvenile rhesus monkey (Macaca mulatta).促性腺激素刺激诱导幼年恒河猴精原细胞分化的睾丸转录组。
Hum Reprod. 2017 Oct 1;32(10):2088-2100. doi: 10.1093/humrep/dex270.
7
A multidisciplinary view on cultural primatology: behavioral innovations and traditions in Japanese macaques.文化灵长类学的多学科视角:日本猕猴的行为创新与传统
Primates. 2016 Jul;57(3):333-8. doi: 10.1007/s10329-016-0518-2. Epub 2016 Feb 10.
8
Sphere-formation culture of testicular germ cells in the common marmoset, a small New World monkey.普通狨猴(一种小型新大陆猴)睾丸生殖细胞的成球培养
Primates. 2016 Jan;57(1):129-35. doi: 10.1007/s10329-015-0500-4. Epub 2015 Nov 3.
9
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Dev Biol. 2015 Apr 1;400(1):43-58. doi: 10.1016/j.ydbio.2015.01.014. Epub 2015 Jan 23.
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