: Recently, we discovered that the bacterial receptor for FimH-expressing bacteria was localized in plasmalemmal caveolae of mast cells and that these caveolae were actively involved in the internalization of the bacteria. Caveolae are subcellular entities rich in glycolipid; and cholesterol and typically contain the scaffolding protein, caveolin. Caveolae mediated bacterial uptake is remarkable because intracellular bacteria remain viable and encased in membranes comprising of caveolar components. Although the significance and scope of caveolae-mediated bacterial uptake by mast cells is, as yet, unknown, this observation represents a novel activity for cellular caveolae in immune cells. To extend our observations, the following specific aims are proposed: (I), Define the scope and molecular basis for caveolae-mediated uptake of bacteria (II), Elucidate the ultimate fate of bacteria internalized via caveolae and (III), Investigate the molecular basis for the caveolae-mediated uptake of FimH-expressing bacteria in human mast cells. Our observations highlighting the role of cellular caveolae in the uptake of bacteria represents an important and novel activity triggered by pathogens in immune cells. The proposed studies should provide new insights into the cellular response of mast cells and possibly other immune cells to infectious agents and provide new clues for devising effective strategies to combat bacterial infections.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI050021-02
Application #
6511601
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Program Officer
Plaut, Marshall
Project Start
2001-07-01
Project End
2006-05-31
Budget Start
2002-06-01
Budget End
2003-05-31
Support Year
2
Fiscal Year
2002
Total Cost
$346,500
Indirect Cost
Name
Duke University
Department
Pathology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
St John, Ashley L; Ang, W X Gladys; Rathore, Abhay P S et al. (2018) Reprograming immunity to food allergens. J Allergy Clin Immunol 141:1936-1939.e2
Miao, Yuxuan; Bist, Pradeep; Wu, Jianxuan et al. (2017) Collaboration between Distinct Rab Small GTPase Trafficking Circuits Mediates Bacterial Clearance from the Bladder Epithelium. Cell Host Microbe 22:330-342.e4
Karhausen, Jörn; Abraham, Soman N (2016) How mast cells make decisions. J Clin Invest 126:3735-3738
Choi, Hae Woong; Abraham, Soman N (2016) Why Serological Responses during Cystitis are Limited. Pathogens 5:
Miao, Yuxuan; Wu, Jianxuan; Abraham, Soman N (2016) Ubiquitination of Innate Immune Regulator TRAF3 Orchestrates Expulsion of Intracellular Bacteria by Exocyst Complex. Immunity 45:94-105
Miao, Yuxuan; Li, Guojie; Zhang, Xiaoli et al. (2015) A TRP Channel Senses Lysosome Neutralization by Pathogens to Trigger Their Expulsion. Cell 161:1306-19
Abraham, Soman N; Miao, Yuxuan (2015) The nature of immune responses to urinary tract infections. Nat Rev Immunol 15:655-63
St John, Ashley L; Ang, W X Gladys; Huang, Min-Nung et al. (2014) S1P-Dependent trafficking of intracellular yersinia pestis through lymph nodes establishes Buboes and systemic infection. Immunity 41:440-450
Bowen, Samantha E; Watt, Christine L; Murawski, Inga J et al. (2013) Interplay between vesicoureteric reflux and kidney infection in the development of reflux nephropathy in mice. Dis Model Mech 6:934-41
St John, Ashley L; Chan, Cheryl Y; Staats, Herman F et al. (2012) Synthetic mast-cell granules as adjuvants to promote and polarize immunity in lymph nodes. Nat Mater 11:250-7

Showing the most recent 10 out of 26 publications