The proteoglycans of human cementum: immunohistochemical localization in healthy, periodontally involved and ageing teeth

Citation
Kt. Ababneh et al., The proteoglycans of human cementum: immunohistochemical localization in healthy, periodontally involved and ageing teeth, J PERIOD RE, 34(2), 1999, pp. 87-96
Citations number
38
Categorie Soggetti
da verificare
Journal title
JOURNAL OF PERIODONTAL RESEARCH
ISSN journal
00223484 → ACNP
Volume
34
Issue
2
Year of publication
1999
Pages
87 - 96
Database
ISI
SICI code
0022-3484(199902)34:2<87:TPOHCI>2.0.ZU;2-6
Abstract
Cementum is believed to play a regulatory role in periodontal regeneration through a variety of macromolecules present in its extracellular matrix (EC M), among which are the proteoglycans (PG). The PG of human cementum have P lot been fully characterized. This study has used a standard indirect immun operoxidase technique to investigate the presence and distribution of PG sp ecies within the ECM of human cementum. Freshly extracted human permanent t eeth were separated into 8 age groups; each group was subdivided to include healthy and periodontally involved teeth, which were then fixed, demineral ized and wax-embedded. Sections were incubated with polyclonal antibodies r ecognizing protein core epitopes in the large chondroitin sulphate PG versi can and the small interstitial PG decorin, biglycan, fibromodulin and lumic an. Immunoreactivity to versican, decorin, biglycan and lumican was evident at the borders and lumina of a proportion of lacunae and canaliculi surrou nding cementocytes in cellular cementum, as well as on inserted periodontal ligament (PDL) fibres. Biglycan was also present along incremental lines i n cellular cementum, whereas staining for fibromodulin was negative. In ace llular cementum, no immunoreactivity was evident with any of the antibodies used except on inserted PDL fibres. These results indicate that versican, decorin, biglycan and lumican are components of the ECM of cellular, but no t of acellular cementum. Neither age nor periodontal diseases appear to qua litatively influence the PG population of cementum. The distribution of PG epitopes around a proportion of cementocytes suggests the existence of diff erent cementocyte subpopulations, or a differential response of these cells to yet undefined stimuli.