| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on December 10, 2002
Accepted on May 28, 2003
1 Monash Institute of Reproduction and Development, Monash University, and Prince Henry's Institute for Medical Research, Melbourne, Australia and Institute of Reproductive Medicine of the University, Münster, Germany
* To whom correspondence should be addressed. E-mail: kate.loveland{at}med.monash.edu.au.
Members of the TGF
superfamily may compete for receptor occupancy and intracellular signaling molecules in specific developmental circumstances. We explored the potential importance of the TGF
family inhibitor, Bambi (Bmp and activin membrane-bound inhibitor) by examining its pattern of mRNA expression in juvenile and adult rat tissues, with a focus on reproductive organs. The 1.8 kb transcript was ubiquitous, while a 3 kb transcript was unique to enriched spermatocyte and spermatid cell fractions and adult testis. The full-length rat cDNA is 89% (nucleic acid) and 95% (amino acid) identical to its human homolog, hnma. Using in situ hybridization, Bambi mRNA was detected in granulosa and theca cells of adult ovaries and in spermatogonia, spermatocytes, round spermatids and Sertoli cells of adult testes. In addition to a persistent signal in Sertoli cells in juvenile testes, this mRNA within germ cells appeared dramatically increased as gonocytes matured into spermatogonia immediately after birth. These data indicate that TGF
superfamily signaling within male germ cells is down-regulated at the onset of spermatogenesis. Addition of exogenous activin A to 24 h cultures of newborn rat testis fragments decreased the Bambi mRNA level. Regulated Bambi mRNA synthesis may contribute to TGF
superfamily signaling modulation in several organs, as suggested by its discrete expression switch in male germ cells.
receptor
BAMBI
spermatogonia
Sertoli cells
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |