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J Dent Res 83(1): 60-64, 2004
© 2004 International and American Associations for Dental Research


RESEARCH REPORT
Biological

Identification of in vivo Pellicle Constituents by Analysis of Serum Immune Responses

J. Li1, E.J. Helmerhorst1, R.F. Troxler1,2, and F.G. Oppenheim1,*,2

1 Department of Periodontology and Oral Biology, Boston University Goldman School of Dental Medicine, 700 Albany Street, Boston, MA 02118, USA; and
2 Department of Biochemistry, Boston University School of Medicine, 715 Albany Street, Boston, MA 02118, USA;

* corresponding author, fropp{at}bu.edu

Human acquired enamel pellicle is composed of molecules that selectively adsorb from saliva onto tooth surfaces and provides a protective interface between the tooth enamel and the oral environment. To identify the micro-amounts of components present in pellicle, we immunized mice with in vivo-formed human acquired enamel pellicle and analyzed the serum immune responses. Selective reactivities of the serum (OD > 1.0 above background) against albumin, amylase, carbonic anhydrase II, sIgA, IgG, IgM, lactoferrin, lysozyme, proline-rich proteins, statherin, histatin 1, and mucous glycoprotein 1 were observed. We further confirmed the presence of proline-rich proteins, lactoferrin, lysozyme, and carbonic anhydrase II by probing in vivo pellicle with specific polyclonal anti-sera. The polyclonal antibody approach provided a powerful method for the identification of various pellicle proteins, including some which show mineral homeostasis or antimicrobial activity.

KEY WORDS: in vivo pellicle • serum • immune response • composition • proteins




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