Male reproductive phenotypes in double mutant mice lacking both FSH beta and activin receptor IIA

Citation
Tr. Kumar et al., Male reproductive phenotypes in double mutant mice lacking both FSH beta and activin receptor IIA, ENDOCRINOL, 142(8), 2001, pp. 3512-3518
Citations number
42
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
ENDOCRINOLOGY
ISSN journal
00137227 → ACNP
Volume
142
Issue
8
Year of publication
2001
Pages
3512 - 3518
Database
ISI
SICI code
0013-7227(200108)142:8<3512:MRPIDM>2.0.ZU;2-2
Abstract
Activins are known to signal through two serine/threonine kinase type II re ceptors. Activin receptor IIA is widely expressed in the male reproductive axis, including the pituitary and testis. Our previous studies using gene k nockout mice have confirmed the essential in vivo role of activin receptor IIA in FSH homeostasis. Activin receptor IIA-null male mice are fertile, ha ve suppressed pituitary and serum FSH levels, and demonstrate a decrease in testis size as a result of reduced Sertoli cells and germ cells. Similarly , FSH beta null male mice are fertile despite reduced testis size and Serto li cell number. To define the direct roles of activin receptor IIA signalin g locally in the testis, independent of its effects on FSH homeostasis, we generated double mutant mice lacking both activin receptor IIA and FSH by a genetic intercross and analyzed the male reproductive phenotypes. The doub le mutant male mice lacking both FSH and activin receptor IIA are fertile, demonstrate no significant reduction in testis size, and produce small litt ers compared with mice lacking either FSH or activin receptor IIA alone. Hi stological analyses of the testes from double mutant mice revealed the pres ence of normal stages of spermatogenesis. However, there was a significant reduction in the epididymal sperm number compared with that of the individu al mutants. Northern blot analyses of total RNA from testes of double mutan ts did not reveal transcriptional up-regulation of activin receptor IIB, th e other activin type II receptor. Although RNA expression profiles of many testis cell-specific markers are unaltered, stereological analysis of the t estes from double mutants indicates that there was a reduction in type A an d I spermatogonial number compared with that observed in individual mutants . Our results provide in vivo genetic evidence to demonstrate that activin receptor IIA signaling plays an important local role within the testis, ind ependent of its actions via FSH homeostasis in the pituitary.