ISSN:
1040-452X
Keywords:
Transforming growth factor-β
;
Mammary
;
Growth regulation
;
Life and Medical Sciences
;
Cell & Developmental Biology
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Biology
Notes:
We have previously shown that TGF-β1 rapidly and reversibly inhibits ductal growth in vivo when administered by miniature slow-release plastic implants. A possible role for endogenous TGF-β1 was suggested by the observation that the normal gland displayed substantial, developmentally regulated levels of TGF-β1 transcripts and protein. These studies have now been extended to include the other two mammalian TGF-β isoforms. When tested with slow-release plastic implants, TGF-β2 and TGF-β3 also caused disappearance of the proliferating mammary stem cell layer, with rapid involution of ductal end buds and cessation of glandular growth. None of the isoforms was active in inhibiting alveolar morphogenesis. We conclude that under the conditions of these tests, the three mammaliian isoforms are functionally equivalent. However, striking differences in patterns of gene expression and in the distribution of immunoreactive peptides suggest that TGF-β2 was expressed only at low levels, and mainly during pregancy. TGF-β3 was expressed in ductal stroma and epithelium, and was the only isoform detected in myoepithelial cells. Developing alveolar tissue and its associated ducts displayed striking TGF-β3 gene expression and immunostaining, which were greatly reduced during lactation. We are now investigating the possibility that the observed high levels of TGF-β expression in pregnancy, particularly of TGF-β3, and the absence of substantial expression of any isoform during lactation, may indicate a role for the TGF-β in regulating functional differentiation or the onset of milk secretion. © 1992 Wiley-Liss, Inc.
Additional Material:
4 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/mrd.1080320210
