Surfactant protein D enhances bacterial antigen presentation by bone marrow-derived dendritic cells

Author:

Brinker Karen G.1,Martin Emily1,Borron Paul1,Mostaghel Elahe2,Doyle Carolyn2,Harding Clifford V.3,Wright Jo Rae14

Affiliation:

1. Departments of Cell Biology,

2. Immunology, and

3. Institute of Pathology, Case Western Reserve University, Cleveland, Ohio 44106

4. Medicine, Duke University Medical Center, Durham, North Carolina 27710; and

Abstract

Surfactant protein (SP) D functions as a soluble pattern recognition molecule to mediate the clearance of pathogens by phagocytes in the innate immune response. We hypothesize that SP-D may also interact with dendritic cells, the most potent antigen presenting cell, to enhance uptake and presentation of bacterial antigens. Using mouse bone marrow-derived dendritic cells, we show that SP-D binds to immature dendritic cells in a dose-, carbohydrate-, and calcium-dependent manner, whereas SP-D binding to mature dendritic cells is reduced. SP-D also binds to Escherichia coli HB101 and enhances its association with dendritic cells. Additionally, SP-D enhances the antigen presentation of an ovalbumin fusion protein expressed in E. coli HB101 to ovalbumin-specific major histocompatibility complex class II T cell hybridomas. The enhancement of antigen presentation by SP-D is dose dependent and is not shared by other collectin-like proteins tested. These studies demonstrate that SP-D augments antigen presentation by dendritic cells and suggest that innate immune molecules such as SP-D may help initiate an adaptive immune response for the purpose of resolving an infection.

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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