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Journal of Dental Research
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Effect of Inflammation on the of Collagen Types, I, III, IV, and V and Type I Trimer and Fibronectin in Human Gingivae

A.S. Narayanan

Department of Pathology

J.A. Clagett

Department of Periodontics and Center for Research in Oral Biology, University of Washington School of Medicine, Seattle, Washington 98195

R.C. Page

Department of Pathology, Departmetn of Periodontics and Center for Research in Oral Biology, University of Washington School of Medicine, Seattle, Washington 98195

The effect of inflammation on the distribution of collagen types I, III, IV, and V and type I trimer and fibronectin in human gingivae was studied after staining them with antibodies to these proteins, Gingival tissues were obtained after periodontal surgery and incubated with antibodies, and staining was visualized by indirect immunofluorescence using FITC- or rhodamine-conjugated second antibodies. The results showed that antibody to type I collagen stained normal gingival connective tissue uniformly and revealed the presence of thick fiber bundles, The staining was sparse at areas of inflammation and leukocytic infiltration. Anti-type-III antibody revealed a fine fibrillar netWork in the normal gingivae, especially near the epithelium; the type III was also lost at sites of inflammation. Type V collagen antibody also stained the gingival connective tissue intensely but, unlike the types I and III staining, it was retained in inflamed areas. Normal gingivae were not stained by the type I trimer antibody; however, staining occurred at inflamed sites. Both normal and inflamed tissues were stained by type IV collagen antibody. and the staining was restricted to basement membrane structures, The normal and inflamed gingivae contained a thick fiber network which bound unti-fibronectin antibody. We conclude that the various ginglvai collagen fibers are made up of collagen types I, III, and V, that the types I and III collagens are preferentially lost during inflammation, and that type I trimer appears at Inflamed sites.

Journal of Dental Research, Vol. 64, No. 9, 1111-1116 (1985)
DOI: 10.1177/00220345850640090201


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