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First published online 8 December 2004
doi: 10.1242/dev.01583
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1 UMR 144 CNRS-Institut Curie, Institut Curie, Section de Recherche, 26 rue
d'Ulm, 75248, Paris, Cedex 05, France
2 Department of Molecular Cell Biology, The Weizmann Institute of Science,
Rehovot, 76100, Israel
* Author for correspondence (e-mail: marina.glukhova{at}curie.fr)
Accepted 12 November 2004
Wnt/ß-catenin signaling pathway is involved in the maintenance of the
progenitor cell population in the skin, intestine and other tissues, and its
aberrant activation caused by stabilization of ß-catenin contributes to
tumorigenesis. In the mammary gland, constitutive activation of
Wnt/ß-catenin signaling in luminal secretory cells results in precocious
lobuloalveolar differentiation and induces adenocarcinomas, whereas the impact
of this signaling pathway on the function of the second major mammary
epithelial cell lineage, the basal myoepithelial cells, has not been analyzed.
We have used the keratin (K) 5 promoter to target the expression of stabilized
N-terminally truncated ß-catenin to the basal cell layer of mouse mammary
epithelium. The transgenic mice presented an abnormal mammary phenotype:
precocious lateral bud formation, increased proliferation and premature
differentiation of luminal epithelium in pregnancy, persistent proliferation
in lactation and accelerated involution. Precocious development in pregnancy
was accompanied by increased Myc and cyclin D1 transcript levels, and a shift
in p63 variant expression towards the
Np63 form. The expression of
ECM-degrading proteinases and their inhibitors was altered in pregnancy and
involution. Nulliparous transgenic females developed mammary hyperplasia that
comprised undifferentiated basal (K5/14-positive, K8- and
-smooth
muscle-actin-negative) cells. Multiparous mice, in addition, developed
invasive basal-type carcinomas. Thus, activation of ß-catenin signaling
in basal mammary epithelial cells affects the entire process of mammary gland
development and induces amplification of basal-type cells that lack lineage
markers, presumably, a subpopulation of mammary progenitors able to give rise
to tumors.
Key words: ß-catenin, Progenitor cell, Mammary gland, Basal epithelial cell, Hyperplasia, Mouse
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