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Transmembrane/cytoplasmic, rather than catalytic, domains of Mmp14 signal to MAPK activation and mammary branching morphogenesis via binding to integrin β1

Mori, Hidetoshi, Lo, Alvin T., Inman, Jamie L., Alcaraz, Jordi, Ghajar, Cyrus M., Mott, Joni D., Nelson, Celeste M., Chen, Connie S., Zhang, Hui, Bascom, Jamie L., Seiki, Motoharu, Bissell, Mina J.·2013·Development
DOI 10.1242/dev.084236
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Abstract

Epithelial cell invasion through the extracellular matrix (ECM) is a crucial step in branching morphogenesis. The mechanisms by which the mammary epithelium integrates cues from the ECM with intracellular signaling in order to coordinate invasion through the stroma to make the mammary tree are poorly understood. Because the cell membrane-bound matrix metalloproteinase Mmp14 is known to play a key role in cancer cell invasion, we hypothesized that it could also be centrally involved in integrating signals for mammary epithelial cells (MECs) to navigate the collagen 1 (CL-1)-rich stroma of the mammary gland. Expression studies in nulliparous mice that carry a NLS-lacZ transgene downstream of the Mmp14 promoter revealed that Mmp14 is expressed in MECs at the tips of the branches. Using both mammary organoids and 3D organotypic cultures, we show that MMP activity is necessary for invasion through dense CL-1 (3 mg/ml) gels, but dispensable for MEC branching in sparse CL-1 (1 mg/ml) gels. Surprisingly, however, Mmp14 without its catalytic activity was still necessary for branching. Silencing Mmp14 prevented cell invasion through CL-1 and disrupted branching altogether; it also reduced integrin β1 (Itgb1) levels and attenuated MAPK signaling, disrupting Itgb1-dependent invasion/branching within CL-1 gels. FRET imaging revealed that Mmp14 associates directly with Itgb1. We identified a domain of Mmp14 that is required for modulating the levels of Itgb1, MEC signaling and the rate of invasion within CL-1. These results shed light on hitherto undescribed non-proteolytic activities of Mmp14 that are necessary for the Itgb1-dependent biochemical and mechanical signals that regulate branching in the mammary epithelium.

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Metadata

Authors
Mori, H., Lo, A. T., Inman, J. L., Alcaraz, J., Ghajar, C. M., Mott, J. D., Nelson, C. M., Chen, C. S., Zhang, H., Bascom, J. L., Seiki, M., & Bissell, M. J.
Affiliations
  • Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
  • Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Venue
Development
Publisher
The Company of Biologists
Published
2013-01-15
Volume
140
Issue
2
Pages
343-352
ISSN
  • 1477-9129
  • 0950-1991
DOI
10.1242/dev.084236
Cited by
104
References
0
Language
en

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