Testicular somatic and germ cell maturation during rhesus macaque development

• 成果类型: Article
• 署名作者: Sosa, Enrique; Wamaitha, Sissy E.; Hsu, Fei-man; Lara, Mary Jasmine D.; Oyama, Kiana; Custer, Maggie; Murphy, Melinda; Hennebold, Jon D.; Hwang, Young Sun; Clark, Amander T.
• 署名单位: University of California System; University of California Los Angeles; University of California System; University of California Los Angeles; University of California System; University of California Los Angeles; Oregon Health & Science University; Oregon National Primate Research Center; Oregon Health & Science University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-10782
• DOI: 10.1073/pnas.2419995122
• 发表日期: 2025-07-01
• 关键词: peritubular myoid cells; anti-mullerian hormone; cynomolgus monkeys; sertoli-cells; fetal dna; testis; gene; protein; spermatogenesis; differentiation

摘要

The formation of bilateral testes in animals is critical for puberty, reproductive capacity, and testosterone production across the life course. In humans, testis development begins in embryonic life in the first trimester, with considerable effort focused on the cell and developmental events associated with testis cell specification, leaving limited knowledge on testicular organogenesis during the second and third trimesters. To fill this knowledge gap, we evaluated testicular cell maturation at weeks 5 (W5), W6, W8, W15, and W19 postconception using a rhesus macaque model. Our data identify a major transcriptional change in the somatic cells of the testis (Sertoli cells, interstitial cells and fetal Leydig cells) between W8 and W15, and this is associated with the maturation of seminiferous cords and maturation of PGCs into fetal spermatogonia. Through this work, we identified cellular changes and differential protein expression between W5 and W19 that can be used to holistically define testis development across the time course of embryonic and fetal life. This study provides important insights necessary to recreate the testicular niche from stem cells for biomedical research.