Molecular and Cellular Biology, December 2000, p. 9092-9101, Vol. 20, No. 23
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030
Received 11 July 2000/Returned for modification 18 August 2000/Accepted 30 August 2000
Heregulin
1 (HRG), a combinatorial ligand for human growth
factor receptors 3 and 4, is a regulatory polypeptide that promotes the
differentiation of mammary epithelial cells into secretory lobuloalveoli. Emerging evidence suggests that the processes of secretory pathways, such as biogenesis and trafficking of vesicles in
neurons and adipose cells, are regulated by the Rab family of
low-molecular-weight GTPases. In this study, we identified Rab3A as a
gene product induced by HRG. Full-length Rab3A was cloned from a
mammary gland cDNA library. We demonstrated that HRG stimulation of
human breast cancer cells and normal breast epithelial cells induces
the expression of Rab3A protein and mRNA in a cycloheximide-independent
manner. HRG-mediated induction of Rab3A expression was blocked by an
inhibitor of phosphatidylinositol 3-kinase but not by inhibitors of
mitogen-activated protein kinases p38MAPK and
p42/44MAPK. Human breast epithelial cells also express
other components of regulated vesicular traffic, such as rabphilin 3A,
Doc2, and syntaxin. Rab3A was predominantly localized in the cytosol,
and HRG stimulation of the epithelial cells also raised the level of
membrane-bound Rab3A. HRG treatment induced a profound alteration in
the cell morphology in which cells displayed neuron-like membrane extensions that contained Rab3A-coated, vesicle-like structures. In
addition, HRG also promoted the secretion of cellular proteins from the
mammary epithelial cells. The ability of HRG to modify exocytosis was
verified by using a growth hormone transient-transfection system.
Analysis of mouse mammary gland development revealed the expression of
Rab3A in mammary epithelial cells. Furthermore, expression of the HRG
transgene in Harderian tumors in mice also enhanced the expression of
Rab3A. These observations provide new evidence of the existence of a
Rab3A pathway in mammary epithelial cells and suggest that it may play
a role in vesicle trafficking and secretion of proteins from epithelial
cells in response to stimulation by the HRG expressed within the
mammary mesenchyma.
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