Întegrins, matrix metalloproteases (MMPs), and the cytokine TGF-β have each been implicated in homeostatic cell behaviors such as cell growth and matrix remodeling. TGF-β exists mainly in a latent state, and a major point of homeostatic control is the activation of TGF-β. Because the latent domain of TGF-β1 possesses an integrin binding motif (RGD), integrins have the potential to sequester latent TGF-β (SLC) to the cell surface where TGF-β activation could be locally controlled. Here, we show that SLC binds to αvβ8, an integrin expressed by normal epithelial and neuronal cells in vivo. This binding results in the membrane type 1 (MT1)-MMP–dependent release of active TGF-β, which leads to autocrine and paracrine effects on cell growth and matrix production. These data elucidate a novel mechanism of cellular homeostasis achieved through the coordination of the activities of members of three major gene families involved in cell–matrix interactions.
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29 April 2002
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April 22 2002
The integrin αvβ8 mediates epithelial homeostasis through MT1-MMP–dependent activation of TGF-β1
Dezhi Mu,
Dezhi Mu
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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Stephanie Cambier,
Stephanie Cambier
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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Lars Fjellbirkeland,
Lars Fjellbirkeland
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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Jody L. Baron,
Jody L. Baron
3Department of Microbiology and Immunology, University of California at San Francisco, San Francisco, CA 94143
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John S. Munger,
John S. Munger
4Department of Medicine and Cell Biology, New York University, New York, NY 10016
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Hisaaki Kawakatsu,
Hisaaki Kawakatsu
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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Dean Sheppard,
Dean Sheppard
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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V. Courtney Broaddus,
V. Courtney Broaddus
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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Stephen L. Nishimura
Stephen L. Nishimura
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
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Dezhi Mu
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
Stephanie Cambier
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
Lars Fjellbirkeland
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
Jody L. Baron
3Department of Microbiology and Immunology, University of California at San Francisco, San Francisco, CA 94143
John S. Munger
4Department of Medicine and Cell Biology, New York University, New York, NY 10016
Hisaaki Kawakatsu
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
Dean Sheppard
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
V. Courtney Broaddus
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
Stephen L. Nishimura
1Department of Pathology, University of California at San Francisco, San Francisco, CA 94143
2University of California at San Francisco/Mt. Zion Cancer Center, University of California at San Francisco, San Francisco, CA 94143
5The Lung Biology Center and Pulmonary Division, San Francisco General Hospital, San Francisco, CA 94110
Address correspondence to Stephen L. Nishimura, Bldg. 3, Rm. 207, San Francisco General Hospital, 1001 Potrero Ave., San Francisco, CA 94110. Tel.: (415) 206-5906. Fax: (415) 206-3765. E-mail: [email protected]
*
Abbreviations used in this paper: ADAM, a disintegrin and a metalloprotease domain; AP, alkaline phosphatase; GFP, green fluorescent protein; LAP, latency-associated peptide; MMP, matrix metalloprotease; MT1-MMP, membrane-type 1 MMP; RT, reverse transcriptase; SLC, latent TGF-β; TSP, thrombospondin; VN, vitronectin.
Received:
September 26 2001
Revision Received:
March 18 2002
Accepted:
March 18 2002
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2002
J Cell Biol (2002) 157 (3): 493–507.
Article history
Received:
September 26 2001
Revision Received:
March 18 2002
Accepted:
March 18 2002
Citation
Dezhi Mu, Stephanie Cambier, Lars Fjellbirkeland, Jody L. Baron, John S. Munger, Hisaaki Kawakatsu, Dean Sheppard, V. Courtney Broaddus, Stephen L. Nishimura; The integrin αvβ8 mediates epithelial homeostasis through MT1-MMP–dependent activation of TGF-β1 . J Cell Biol 29 April 2002; 157 (3): 493–507. doi: https://doi.org/10.1083/jcb.200109100
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