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RESEARCH PAPER / 2025-09-30

Aging-TCA: a cross-species single-cell transcriptomic atlas for studying testicular aging.

Zhihao Lu, Ziyan Zhang, Lingsheng Cao, Gangcai Xie

Institute of Reproductive Medicine, Medical School, Nantong University, Qixiu Road 19, Nantong, 226001, China. · pubmed

Abstract

The testis, with the highest number of transcriptionally active genes among human tissues, offers a unique window into how aging affects complex gene regulation. Recent advancements in single-cell RNA sequencing have enabled multi-species studies of aging-related transcriptome changes in testes. However, a comprehensive aging-related cross-species platform for analyzing testicular single-cell transcriptomes remains absent. To address this gap, we developed Aging-TCA (Aging-related Testicular Cell Atlas, available at http://tca.xielab.tech/)—a comprehensive online platform containing aging-related testicular single cell and spatial transcriptome profiles from human, cynomolgus monkey, mouse, and zebrafish across 89 samples and over 460, 000 testicular cells, nuclei or spots. Aging-TCA provides versatile tools for temporal and spatial analyzing testicular aging, including aging-related testicular gene expression visualization, cell-cell communication comparisons, cell-trajectory analysis, gene regulatory network analysis, testicular cell type auto-identification, time-series analysis, and spatial transcriptome comparisons. In summary, we provide a novel platform Aging-TCA for advancing cross-species research into testicular aging, facilitating future investigations in this field.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper presents a comprehensive online platform for analyzing aging-related testicular single-cell transcriptomes across multiple species. This research is relevant as it addresses the mechanisms of aging at a cellular level, contributing to the understanding of the biological processes involved in aging.

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