Testicular somatic and germ cell maturation during rhesus macaque development

E Enrique Sosa (Department of Molecular, Cell and Developmental Biology, University of California Los Angeles) S Sissy E. Wamaitha (Department of Molecular, Cell and Developmental Biology, University of California Los Angeles) F Fei-man Hsu (Department of Molecular, Cell and Developmental Biology, University of California Los Angeles) M Mary Jasmine D. Lara (Department of Molecular, Cell and Developmental Biology, University of California Los Angeles) K Kiana Oyama (Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center) M Maggie Custer (Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center) M Melinda Murphy (Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center) J Jon D. Hennebold (Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center) Y Young Sun Hwang (Department of Molecular, Cell and Developmental Biology, University of California Los Angeles) A Amander T. Clark (Department of Molecular, Cell and Developmental Biology, University of California Los Angeles)

Abstract

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.

Article Details

Volume / Issue Vol. 122, Issue 26
Published July 01, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

E

Enrique Sosa

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles

S

Sissy E. Wamaitha

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles

F

Fei-man Hsu

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles

M

Mary Jasmine D. Lara

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles

K

Kiana Oyama

Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center

M

Maggie Custer

Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center

M

Melinda Murphy

Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center

J

Jon D. Hennebold

Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center

Y

Young Sun Hwang

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles

A

Amander T. Clark

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles