The overall objective of this program is to enhance our understanding of the mechanisms that regulate wound healing and epithelial mucosal defense against infection with particular reference to the lung epithelium. Because each of the four projects in this program require a coordinated cell culture facility to evaluate in vitro epithelial repair, a cell isolation and culture core is proposed to provide a central resource available to all investigators for evaluating and testing mechanisms relevant to their individual projects. The primary aims of this cell culture core are (1) to provide a mechanism for generating primary cell isolation of alveolar epithelial cells from rat and mouse lungs that can be used to study in vitro mechanisms of epithelial injury and repair, (2) to provide primary isolation of human alveolar epithelial type II cells from cadaver human lungs to evaluate the mechanisms of epithelial injury and repair in human lung epithelium, (3) to provide a centralized location for the measurement of in vitro epithelial wound repair that can be useful for all projects using either primary cell isolation or cell lines. Dr. Matthay and his laboratory have considerable experience with the primary isolation of rodent lung epithelial cell lines, and recently have developed methodology to isolate purified alveolar epithelial type II cells from human cadaver lungs, providing a unique resource for this program. Also, this cell isolation and culture core will provide useful expertise for studying in vitro mechanisms of lung epithelial cell repair.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI053194-01
Application #
6588023
Study Section
Special Emphasis Panel (ZAI1)
Project Start
2002-12-01
Project End
2007-11-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Datta, Anirban; Sandilands, Emma; Mostov, Keith E et al. (2017) Fibroblast-derived HGF drives acinar lung cancer cell polarization through integrin-dependent RhoA-ROCK1 inhibition. Cell Signal 40:91-98
Singer, Mark S; Phillips, Joanna J; Lemjabbar-Alaoui, Hassan et al. (2015) SULF2, a heparan sulfate endosulfatase, is present in the blood of healthy individuals and increases in cirrhosis. Clin Chim Acta 440:72-8
Plaks, Vicki; Boldajipour, Bijan; Linnemann, Jelena R et al. (2015) Adaptive Immune Regulation of Mammary Postnatal Organogenesis. Dev Cell 34:493-504
Casbon, Amy-Jo; Reynaud, Damien; Park, Chanhyuk et al. (2015) Invasive breast cancer reprograms early myeloid differentiation in the bone marrow to generate immunosuppressive neutrophils. Proc Natl Acad Sci U S A 112:E566-75
Bucior, Iwona; Tran, Cindy; Engel, Joanne (2014) Assessing Pseudomonas virulence using host cells. Methods Mol Biol 1149:741-55
Bonnans, Caroline; Lohela, Marja; Werb, Zena (2014) Real-time imaging of myeloid cells dynamics in ApcMin/+ intestinal tumors by spinning disk confocal microscopy. J Vis Exp :51916
Tran, Cindy S; Eran, Yoni; Ruch, Travis R et al. (2014) Host cell polarity proteins participate in innate immunity to Pseudomonas aeruginosa infection. Cell Host Microbe 15:636-43
Kwon, Sang-Ho; Liu, Kathleen D; Mostov, Keith E (2014) Intercellular transfer of GPRC5B via exosomes drives HGF-mediated outward growth. Curr Biol 24:199-204
Kim, J H; Chan, C; Elwell, C et al. (2013) Endosulfatases SULF1 and SULF2 limit Chlamydia muridarum infection. Cell Microbiol 15:1560-71
Maltseva, Inna; Chan, Matilda; Kalus, Ina et al. (2013) The SULFs, extracellular sulfatases for heparan sulfate, promote the migration of corneal epithelial cells during wound repair. PLoS One 8:e69642

Showing the most recent 10 out of 80 publications