LOCALIZATION OF CARBOXY-TERMINAL TYPE-II PROCOLLAGEN PEPTIDE (PCOL-II-C) AND TYPE-II COLLAGEN IN THE REPAIR TISSUE OF FULL-THICKNESS ARTICULAR-CARTILAGE DEFECT

Citation
H. Nakajima et al., LOCALIZATION OF CARBOXY-TERMINAL TYPE-II PROCOLLAGEN PEPTIDE (PCOL-II-C) AND TYPE-II COLLAGEN IN THE REPAIR TISSUE OF FULL-THICKNESS ARTICULAR-CARTILAGE DEFECT, Connective tissue research (Print), 37(3-4), 1998, pp. 195
Citations number
29
Categorie Soggetti
Orthopedics,"Cell Biology
ISSN journal
03008207
Volume
37
Issue
3-4
Year of publication
1998
Database
ISI
SICI code
0300-8207(1998)37:3-4<195:LOCTPP>2.0.ZU;2-O
Abstract
It is well established that a full-thickness articular cartilage defec t is repaired with a fibrocartilaginous tissue of which cells are deri ved from undifferentiated mesenchymal stem cells in the bone marrow. T o characterize the repair tissue immunohistochemically, full-thickness defects were created in rabbit knee joints, and the repair tissues im munostained at 3, 6, and 12 weeks after surgery. Well characterized po lyclonal antibody against carboxyterminal type II procollagen peptide (pCOL-II-C) and monoclonal antibody against type II collagen were used to evaluate the repair tissue with regard to the metabolism of type I I collagen. Immunohistochemistry revealed that pCOL-II-C was localized in or around most of the repair cells obtained at 3 and 6 weeks after surgery, while type II collagen distributed mainly in the pericellula r matrix of metaplastic round-shaped repair cells. The results suggest that the repair cells taken at the early stage of the repair process of the defect could originally have more activity of type II collagen synthesis.