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Publication : Age-related bone deterioration is diminished by disrupted collagen sensing in integrin α2β1 deficient mice.

First Author  Stange R Year  2013
Journal  Bone Volume  56
Issue  1 Pages  48-54
PubMed ID  23680479 Mgi Jnum  J:203557
Mgi Id  MGI:5527470 Doi  10.1016/j.bone.2013.05.003
Citation  Stange R, et al. (2013) Age-related bone deterioration is diminished by disrupted collagen sensing in integrin alpha2beta1 deficient mice. Bone 56(1):48-54
abstractText  Collagen binding integrins are of essential importance in the crosstalk between cells and the extracellular matrix. Integrin alpha2beta1 is a major receptor for collagen I, the most abundant protein in bone. In this study we show for the first time that integrin alpha2 deficiency is linked to collagen type I expression in bone. Investigating the femurs of wild type and integrin alpha2beta1 deficient mice, we found that loss of integrin alpha2 results in altered bone properties. Histomorphometric analysis of integrin alpha2 long bones displayed more trabecular network compared to wild type bones. During age related bone loss the integrin alpha2beta1 deficient bones retain trabecular structure even at old age. These findings were supported by functional, biomechanical testing, wherein the bones of integrin alpha2beta1 deficient mice do not undergo age-related alteration of biomechanical properties. These results might be explained by the increased presence of collagen in integrin alpha2beta1 deficient bone. Collagen type I could be detected in higher quantities in the integrin alpha2beta1 deficient bones, forming abnormal, amorphous fibrils. This was linked to higher expression levels of collagen type I and other bone formation related proteins as alkaline phosphatase of integrin alpha2beta1 deficient osteoblasts. Osteoclasts of integrin alpha2beta1 deficient mice did not show any differences. Consequently these results indicate that the absence of integrin alpha2beta1 alleviates the effects of age related bone degradation through over-expression of collagen type I and demonstrate a molecular mechanism how collagen binding integrins might directly impact bone aging.
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