FXIIIA and TGF-β over-expression produces normal musculo-skeletal phenotype in TG2-/- mice

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作者
U. Tarantino
F. Oliva
G. Taurisano
A. Orlandi
V. Pietroni
E. Candi
G. Melino
N. Maffulli
机构
[1] University of Rome “Tor Vergata”,Department of Orthopaedics and Traumatology
[2] University of Rome “Tor Vergata”,Department of Anatomic Pathology
[3] University of Rome “Tor Vergata”,Department of Experimental Medicine and Biochemical Sciences
[4] Keele University School of Medicine,Department of Trauma and Orthopaedic Surgery
来源
Amino Acids | 2009年 / 36卷
关键词
Endochondral ossification; Transglutaminase;
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摘要
Transglutaminase (TGs) enzymes and proteins crosslinking have for long time been implicated in the formation of hard tissue development, matrix maturation and mineralization. Among the TGs family members, in the context of connective tissue formation, TG2 and Factor XIII are expressed in cartilage by hypertrophic chondrocytes. Here, we analyse the morphological consequences of TG2 deficiency, during the development of skeletal elements. When TG2 is absent, there are not gross abnormalities in the development of the skeletal system, probably from compensatory mechanisms resulting in increased expression of FXIIIA and TGF-ß 1. In vivo other TGs may be involved in promoting chondrocytes and osteoblast differentiation and matrix mineralisation
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