Iowa Section of AADR - The University of Iowa College of Dentistry
Iowa Section of AADR - The University of Iowa College of Dentistry
Iowa Section of AADR - The University of Iowa College of Dentistry
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R01 DEO14390.<br />
Supported by: <strong>University</strong> <strong>of</strong> <strong>Iowa</strong>, <strong>College</strong> <strong>of</strong> <strong>Dentistry</strong>, <strong>Iowa</strong> Dental Research Grant<br />
4. HBD3 Inhibits Porphyromonas gingivalis rHagB Binding to Dendritic Cells<br />
J. Van Hemert 5 , E. Recker 5 , K. Walters 2 , A. Progulske-Fox 6 , K.A. Brogden 5<br />
2 <strong>University</strong> <strong>of</strong> <strong>Iowa</strong>, <strong>Iowa</strong> City, IA; 5 <strong>University</strong> <strong>of</strong> <strong>Iowa</strong> <strong>College</strong> <strong>of</strong> <strong>Dentistry</strong>, <strong>Iowa</strong> City, IA; 6 <strong>University</strong> <strong>of</strong> Florida,<br />
Gainesville, FL<br />
Human β-defensin 3 (HBD3) is a small, well-characterized peptide with broad antimicrobial activities and<br />
diverse innate immune functions. Previously, we found that HBD3 binds to recombinant Porphyromonas gingivalis<br />
dendritic cells.<br />
Objectives: Our objective was to determine if HBD3 binding to rHagB alters the binding <strong>of</strong> rHagB to the surface <strong>of</strong><br />
human myeloid dendritic cells.<br />
Methods: To test this, human myeloid dendritic cells and mouse JAWS II cells were incubated with 0.1 μM<br />
rHagB, 1.0 μM HBD3+0.1 μM rHagB (10:1 molar ratio), 1.0 μM HBD3, or 0.1 M PBS, pH 7.2. After 5 minutes,<br />
with monoclonal MoAb 1858 to rHagB, polyclonal rabbit to rHagB, and polyclonal 500-P241 rabbit antibody to<br />
microscopy.<br />
Results: For confocal microscopy, 6.3 x 104 dendritic cells in chamber slides were incubated with rHagB and had<br />
Conclusion: Overall, these results strongly suggest that HBD3 binding to rHagB alters the binding <strong>of</strong> rHagB to the<br />
response <strong>of</strong> rHagB in dendritic cells. This work was supported by NIH, NIDCR grant R01 DEO14390.<br />
Supported by: NIH, NIDCR grant R01 DEO14390.<br />
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