About Us |
PMID | 14745012 |
Gene Name | AR |
Condition | Causes spermatogenic arrest in meiosis |
Association |
Associated |
Sex | Male |
Infertility type | Male infertility |
A Sertoli cell-selective knockout of the androgen receptor causes spermatogenic arrest in meiosis De Gendt K, Swinnen JV, Saunders PT, Schoonjans L, Dewerchin M, Devos A, Tan K, Atanassova N, Claessens F, Lécureuil C, Heyns W, Carmeliet P, Guillou F, Sharpe RM, Verhoeven G. Androgens control spermatogenesis, but germ cells themselves do not express a functional androgen receptor (AR). Androgen regulation is thought to be mediated by Sertoli and peritubular myoid cells, but their relative roles and the mechanisms involved remain largely unknown. Using Cre/loxP technology, we have generated mice with a ubiquitous knockout of the AR as well as mice with a selective AR knockout in Sertoli cells (SC) only. Mice with a floxed exon 2 of the AR gene were crossed with mice expressing Cre recombinase ubiquitously or selectively in SC (under control of the anti-Müllerian hormone gene promoter). AR knockout males displayed a complete androgen insensitivity phenotype. Testes were located abdominally, and germ cell development was severely disrupted. In contrast, SC AR knockout males showed normal testis descent and development of the male urogenital tract. Expression of the homeobox gene Pem, which is androgen-regulated in SC, was severely decreased. Testis weight was reduced to 28% of that in WT littermates. Stereological analysis indicated that the number of SC was unchanged, whereas numbers of spermatocytes, round spermatids, and elongated spermatids were reduced to 64%, 3%, and 0% respectively of WT. These changes were associated with increased germ cell apoptosis and grossly reduced expression of genes specific for late spermatocyte or spermatid development. It is concluded that cell-autonomous action of the AR in SC is an absolute requirement for androgen maintenance of complete spermatogenesis, and that spermatocyte/spermatid development/survival critically depends on androgens. FAU - De Gendt, Karel AU - De Gendt K AD - Laboratory for Experimental Medicine and Endocrinology, Department of Developmental Biology, Flanders Interuniversity Institute for Biotechnology, Catholic University of Leuven, B-3000 Leuven, Belgium. FAU - Swinnen, Johannes V AU - Swinnen JV FAU - Saunders, Philippa T K AU - Saunders PT FAU - Schoonjans, Luc AU - Schoonjans L FAU - Dewerchin, Mieke AU - Dewerchin M FAU - Devos, Ann AU - Devos A FAU - Tan, Karen AU - Tan K FAU - Atanassova, Nina AU - Atanassova N FAU - Claessens, Frank AU - Claessens F FAU - Lécureuil, Charlotte AU - Lécureuil C FAU - Heyns, Walter AU - Heyns W FAU - Carmeliet, Peter AU - Carmeliet P FAU - Guillou, Florian AU - Guillou F FAU - Sharpe, Richard M AU - Sharpe RM |