Transglutaminase factor XIIIA in the cartilage of developing avian long bones

• Published in: Developmental dynamics Vol. 223; no. 1; pp. 24 - 32
• Main Authors: Nurminskaya, M.V., Recheis, B., Nimpf, J., Magee, Cordula, Linsenmayer, T.F.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 01.01.2002
• Subjects: Animals; avian; Bone Development; cartilage; Cartilage - cytology; Cartilage - enzymology; Cartilage - growth & development; Cells, Cultured; Chick Embryo; Collagen Type X - metabolism; factor XIIIA; Factor XIIIa - metabolism; Growth Plate - cytology; Growth Plate - enzymology; Growth Plate - metabolism; Immunohistochemistry; Osteogenesis; Tarsus, Animal - cytology; Tarsus, Animal - enzymology; transglutaminase
• ISSN: 1058-8388; 1097-0177
• DOI: 10.1002/dvdy.1230

Previously, we showed that mRNA for transglutaminase factor XIIIA (FXIIIA) is up‐regulated in the hypertrophic zone of the growth plate of the chicken tibiotarsus, a well‐characterized model of long bone development. In the present study, we have studied the distribution of the FXIIIA protein and of transglutaminase enzymatic activity in this growth plate, as well as in the cartilage of the epiphysis, which includes that of the articular surface. By immunohistochemical analysis, the protein is detected in the zone of maturation, where it is mostly intracellular, and in the hypertrophic zone, where it is present both intracellularly and in the extracellular matrix. The intracellular enzyme is mostly a zymogen, as determined with an antibody specific for the activation peptide. Externalization of FXIIIA is accompanied by enzyme activation. To study the pattern of transglutaminase activity, a synthetic transglutaminase substrate, rhodamine‐conjugated tetrapeptide (Pro‐Val‐Lys‐Gly), was used for pulse labeling in organ cultures. Intensive incorporation of the fluorescent substrate was observed throughout the hypertrophic zone and in the cells surrounding the forming blood vessels. The patterns of FXIIIA immunostaining and substrate incorporation overlap almost completely. The cartilaginous factor XIIIA is different from the plasma form in that, both intracellularly and extracellularly, it exists as a monomer, as determined by Western analysis, whereas the plasma form of FXIII is a tetrameric complex composed of both A and B subunits. We also identified FXIIIA and transglutaminase activity within the articular and condylar regions of the tarsus, suggesting a possible involvement of mechanical pressure and/or stress in the production of the molecule and subsequent cross‐linking of the cartilage matrix. Thus, transglutaminases, in particular FXIIIA, are involved in the formation of long bones through its activity both in the hypertrophic region of the growth plate and in the formation of articular/epiphyseal cartilages. © 2001 Wiley‐Liss, Inc.