| Autor: |
Bozhokin MS; Vreden Russian Scientific Research Institute of Traumatology and Orthopedics, St. Petersburg, 195427, Russia. writeback@mail.ru.; Institute of Cytology, Russian Academy of Science, St. Petersburg, 194064, Russia., Sopova YV; Vavilov Institute of General Genetics, Russian Academy of Science, St. Petersburg Branch, St. Petersburg, 199034, Russia.; St. Petersburg State University, Faculty of Biology, St. Petersburg, 199034, Russia.; St. Petersburg State University, Laboratory of Amyloid Biology, St. Petersburg, 199034, Russia., Kachkin DV; St. Petersburg State University, Faculty of Biology, St. Petersburg, 199034, Russia.; St. Petersburg State University, Laboratory of Amyloid Biology, St. Petersburg, 199034, Russia., Rubel AA; St. Petersburg State University, Faculty of Biology, St. Petersburg, 199034, Russia.; St. Petersburg State University, Laboratory of Amyloid Biology, St. Petersburg, 199034, Russia., Khotin MG; Institute of Cytology, Russian Academy of Science, St. Petersburg, 194064, Russia. |
| Abstrakt: |
Hyaline cartilage is a nonvascular connective tissue covering the joint surface. It consists mostly of the extracellular matrix proteins and a small number of highly differentiated chondrocytes. At present, various techniques for repairing joint surfaces damage, for example, the use of modified cell cultures and biodegradable scaffolds, are under investigation. Molecular mechanisms of cartilage tissue proliferation have been also actively studied in recent years. TGFβ3, which plays a critical role in the proliferation of normal cartilage tissue, is one of the most important protein among cytokines and growth factors affecting chondrogenesis. By interacting directly with receptors on the cell membrane surface, TGFβ3 triggers a cascade of molecular interactions involving transcription factor Sox9. In this review, we describe the effects of TGFβ3 on the receptor complex activation and subsequent intracellular trafficking of Smad proteins and analyze the relation between these processes and upregulation of expression of major extracellular matrix genes, such as col2a1 and acan. |
