Title

Integrin beta4 regulation of PTHrP underlies its contribution to mammary gland development

UMMS Affiliation

Department of Molecular, Cell and Cancer Biology

Date

11-15-2015

Document Type

Article

Disciplines

Developmental Biology

Abstract

The integrin alpha6beta4 (referred to as beta4) is expressed in epithelial cells where it functions as a laminin receptor. Although in vitro studies have implicated beta4 in the biology of mammary epithelial cells, its contribution to mammary gland development has not been settled. To address this problem, we generated and analyzed itgb4(flox/flox)MMTV-Cre(-) and itgb4(flox/flox)MMTV-Cre(+) mice. The salient features of embryonic mammary tissue from itgb4(flox/flox)MMTV-Cre(+) mice were significantly smaller mammary buds and increased apoptosis in the surrounding mesenchyme. Also, compared to control glands, the itgb4-deleted mammary buds lacked expression of the progenitor cell marker CK14 and they were unable to generate mammary glands upon transplantation into cleared fat pads of recipient mice. Analysis of mammary glands at puberty and during pregnancy revealed that itgb4-diminished mammary tissue was unable to elongate and undergo branching morphogenesis. Micro-dissection of epithelial cells in the mammary bud and of the surrounding mesenchyme revealed that loss of beta4 resulted in a significant decrease in the expression of parathyroid hormone related protein (PTHrP) in epithelial cells and of target genes of the PTHrP receptor in mesenchymal cells. Given that the phenotype of the itgb4-deleted mammary tissue mimicked that of the PTHrP knockout, we hypothesized that beta4 contributes to mammary gland development by sustaining PTHrP expression and enabling PTHrP signaling. Indeed, the inability of itgb4-deleted mammary buds to elongate was rescued by exogenous PTHrP. These data implicate a critical role for the beta4 integrin in mammary gland development and provide a mechanism for this role.

Rights and Permissions

Citation: Dev Biol. 2015 Nov 15;407(2):313-20. doi: 10.1016/j.ydbio.2015.09.015. Epub 2015 Sep 30. Link to article on publisher's site

Related Resources

Link to Article in PubMed

PubMed ID

26432258