Mapping the immune cells of the testis: Key insights into sexual maturation.

IF 3.2 2区 医学 Q1 ANDROLOGY
Andrology Pub Date : 2025-06-06 DOI:10.1111/andr.70077
Xiaoyu Wu, Chenzhao Feng, Zunpan Fan, Yongfeng Wang, Huiping Zhang, Kai Zhao
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引用次数: 0

Abstract

Background: The testicular immune microenvironment sustains homeostasis and immune privilege. However, the presence and functional significance of B cells within this specialized niche remain poorly characterized. Furthermore, the intricate crosstalk between resident immune populations and testicular stromal cells that may orchestrate the immunological and endocrine microenvironment during sexual maturation warrants systematic investigation.

Objective: To systematically delineate the immune cell atlas and developmental trajectory of testicular leukocytes before and after sexual maturation.

Materials and methods: An integrated analysis of leukocytes in post-sexual maturity (8-week-old) and pre-sexual maturity (2-week-old) mouse testes using single-cell RNA sequencing (scRNA-seq) and mass cytometry (CyTOF), was performed. Magnetic-activated cell sorting (MACS) isolated immune subsets, followed by bioinformatics interrogation of cellular heterogeneity and ligand-receptor network analysis to map intercellular communication pathways.

Results: Through scRNA-seq clustering analysis, we resolved 18 distinct leukocyte populations (11 lymphoid and seven myeloid lineages), which were further validated and expanded to 17 phenotypically discrete subsets (eight lymphoid and nine myeloid) via high-dimensional CyTOF profiling. Notably, we identified a rare but functionally significant B lymphocyte population within the testicular compartment. The myeloid compartment exhibited pronounced developmental plasticity, marked by progressive Il1b+Macrophages diminution and regulatory T cell expansion during maturation. Cell communication network analysis revealed intensified ligand-receptor cross-talk between androgen-producing Leydig cells and CD8+ T lymphocytes in post-pubertal testes, providing mechanistic insights into age-dependent immune privilege establishment.

Discussion and conclusions: Multi-omics integration reveals dynamic immune remodeling during testicular maturation. These findings underscore the potential involvement of B cells in local immune surveillance while identifying maturation-associated signaling axes between stromal and immune cells. This comprehensive mapping of testicular leukocyte dynamics significantly advances our understanding of reproductive immunology and lays foundation for investigating immune-mediated testicular pathologies.

绘制睾丸免疫细胞:性成熟的关键见解。
背景:睾丸免疫微环境维持体内平衡和免疫特权。然而,在这个特殊的生态位中,B细胞的存在和功能意义仍然很不清楚。此外,在性成熟过程中,常驻免疫群体和睾丸基质细胞之间复杂的串扰可能会协调免疫和内分泌微环境,这需要系统的研究。目的:系统地描述性成熟前后睾丸白细胞的免疫细胞图谱和发育轨迹。材料和方法:采用单细胞RNA测序(scRNA-seq)和细胞计数技术(CyTOF)对性成熟后(8周龄)和性成熟前(2周龄)小鼠睾丸中的白细胞进行了综合分析。磁激活细胞分选(MACS)分离免疫亚群,随后进行细胞异质性的生物信息学研究和配体-受体网络分析,以绘制细胞间通讯途径。结果:通过scRNA-seq聚类分析,我们确定了18个不同的白细胞群(11个淋巴细胞谱系和7个髓细胞谱系),并通过高维CyTOF分析进一步验证并扩展到17个表型离散亚群(8个淋巴细胞谱系和9个髓细胞谱系)。值得注意的是,我们在睾丸室中发现了一种罕见但功能显著的B淋巴细胞群。髓系室表现出明显的发育可塑性,在成熟过程中表现为进行性il - 1b+巨噬细胞减少和调节性T细胞扩增。细胞通讯网络分析显示,在青春期后的睾丸中,产生雄激素的间质细胞和CD8+ T淋巴细胞之间的配体-受体互导增强,为年龄依赖性免疫特权的建立提供了机制见解。讨论与结论:多组学整合揭示了睾丸成熟过程中的动态免疫重塑。这些发现强调了B细胞在确定基质细胞和免疫细胞之间的成熟相关信号轴时可能参与局部免疫监视。这种全面的睾丸白细胞动力学图谱显著地促进了我们对生殖免疫学的理解,并为研究免疫介导的睾丸病理奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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