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Blood, 15 February 2006, Vol. 107, No. 4, pp. 1636-1642.
Prepublished online as a Blood First Edition Paper on November 1, 2005; DOI 10.1182/blood-2005-06-2559.
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Submitted June 29, 2005
Accepted October 12, 2005
Exogenous Heat Shock Protein-70 binds macrophage-lipid raft-microdomain and stimulates phagocytosis, processing and MHC-II presentation of antigens
Ruibo Wang, Joseph T Kovalchin, Peggy Muhlenkamp, and Rajiv Y Chandawarkar*
Division of Plastic Surgery, Department of Surgery, Center for Immunotherapy, University of Connecticut School of Medicine, Farmington, CT, USA
* Corresponding author; email: chandawarkar{at}uchc.edu.
The extracellular presence of endotoxin-free Heat Shock Protein 70 (HSP70) enhances the rate and capacity of macrophage-mediated phagocytosis at 6 times the basal rate. It is protein-specific, dose- and time-dependent and involves the internalization of inert microspheres, gram-positive and -negative bacteria and fungi. Structurally, exogenous HSP70 binds the macrophage plasma membrane, specifically on its lipid raft-microdomain. Disruption of lipid rafts, HSP70-LR interaction or denaturing HSP70 abrogates the HSP-mediated increase in phagocytosis. Further, HSP70-mediated phagocytosis directly enhances the processing and presentation of internalized antigens via the endocytic MHC class-II pathway to CD4+ T lymphocytes. Modulating the HSP70-LR interaction presents an opportunity to intervene at the level of host pathogen interface; a therapeutic tool for emerging infections, especially where conventional treatment with antibiotics is ineffective (antibiotic resistance) or unavailable (rapidly spreading). These results identify a new role for HSP70, a highly conserved molecule in stimulating phagocytosis - a primordial macrophage function thereby influencing both innate and adaptive immune responses.

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