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| Ashrafi, Kaveh |
| Barber, Diane L |
| Bernstein, Harold S. |
| Black, Brian L |
| Blanc, Paul D |
| Boushey, Homer A |
| Broaddus, V Courtney |
| Brown, James K |
| Caughey, George H |
| Chapman, Harold A |
| Charo, Israel F |
| Chatterjee, Kanu |
| Chuang, Pao-Tien |
| Clyman, Ronald I |
| Conklin, Bruce R |
| Coughlin, Shaun R |
| Derynck, Rik M |
| Dobbs, Leland G |
| Eisner, Mark D |
| Engel, Joanne N |
| Erle, David J |
| Fahy, John Vincent |
| Farese, Robert V |
| Fielding, Christopher J |
| Fielding, Phoebe |
| Fineman, Jeffrey R |
| Glantz, Stanton A |
| Grossman, William |
| Hawgood, Samuel |
| Ingraham, Holly A |
| Jan, Lily Y |
| Kan, Yuet W |
| Kane, John P |
| Kornberg, Thomas B |
| Kurtz, Theodore W |
| Kwok, Pui-Yan |
| Lazarus, Stephen C |
| Malloy, Mary J. |
| Martin, Gail R |
| Matthay, Michael A |
| Mcdonald, Donald M |
| Mikawa, Takashi |
| Minor, Daniel L |
| Mostov, Keith E |
| Nadel, Jay A |
| Ordahl, Charles P |
| Pitas, Robert E |
| Reiter, Jeremy F. |
| Rosen, Steven D |
| Shaw, Robin M. |
| Sheppard, Dean |
| Simpson, Paul C |
| Stainier, Didier Y. R. |
| Wang, Rong |
| Weiner, Orion D |
| Weisgraber, Karl H |
| Weiss, Arthur |
| Weiss, Ethan J |
| Werb, Zena |
| Wiener-Kronish, Jeanine |
| Young, William L |
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CVRI Scientists
Harold A. Chapman, M.D.
Professor of Medicine; Chief, Division of Pulmonary and Critical Care Medicine
Research Interests:
Antigen presentation by MHC class II molecules important to immunity and autoimmunity and extracellular matrix remodeling important to cell migration and tissue repair
Summary:
Integrins are a well known family of cell surface adhesion protein receptors. Integrins attach to the matrix surrounding cells, and neighboring cells and convey information to the cell allowing it to respond. For example, cells suddenly devoid of their integrin attachments to their surrounding matrix frequently undergo a cell death program. Integrin function therefore affects cellular differentiation state, survival, growth, and movement. My lab has been studying a set of integrins widely expressed on epithelial cells and attempting to understand how the information conveyed by these integrins is regulated and whether there are critical pathways of signaling initiated through integrins that are needed for tumor progression and wound healing. The lab is primarily focused on the lung and hence our experimental models are mainly intended to model pulmonary fibrosis (scarring) and lung cancer.
The main objectives of our current studies related to integrins are to understand integrin function in the context of epithelial cell transdifferentiation to fibroblast-like cells during lung repair (wound healing) and in the context of transformed epithelial cell (carcinoma) metastasis to and within the lung. We believe both of these processes may be critically dependent on integrins.
More detailed descriptions of current projects related to integrins as well as to the cathepsin (endosomal protease) part of the lab, current lab members, and recent publications, are provided within the lab website link (pulmonary.ucsf.edu/chapmanlab).
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