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Lookup NU author(s): Emeritus Professor Tim Cawston, Professor David YoungORCiD
The joint is a discrete unit that consists of cartilage, bone, tendon and ligaments. These tissues are all composed of an extracellular matrix made of collagens, proteoglycans and specialised glycoproteins that are actively synthesised, precisely assembled and subsequently degraded by the resident connective tissue cells. A balance is maintained between matrix synthesis and degradation in healthy adult tissues. Different classes of proteinases play a part in connective tissue turnover in which active proteinases can cleave matrix protein during resorption, although the proteinase that predominates varies between different tissues and diseases. The metalloproteinases are potent enzymes that, once activated, degrade connective tissue and are inhibited by tissue inhibitors of metalloproteinases (TIMPs); the balance between active matrix metalloproteinases and TIMPs determines, in many tissues, the extent of extracellular matrix degradation. The serine proteinases are involved in the initiation of activation cascades and some, such as elastase, can directly degrade the matrix. Cysteine proteinases are responsible for the breakdown of collagen in bone following the removal of the osteoid layer and the attachment of osteoclasts to the exposed bone surface. Various growth factors increase the synthesis of matrix and proteinase inhibitors, whereas cytokines ( alone or in combination) can inhibit matrix synthesis and stimulate proteinase production and matrix destruction.
Author(s): Cawston TE, Young DA
Publication type: Review
Publication status: Published
Journal: Cell and Tissue Research
Year: 2010
Volume: 339
Issue: 1
Pages: 221-235
ISSN (print): 0302-766X
ISSN (electronic): 1432-0878
Publisher: SPRINGER
URL: http://dx.doi.org/10.1007/s00441-009-0887-6
DOI: 10.1007/s00441-009-0887-6
