4.5 Article

Defining matrix Gla protein expression in the Dunkin-Hartley guinea pig model of spontaneous osteoarthritis

期刊

BMC MUSCULOSKELETAL DISORDERS
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12891-021-04735-2

关键词

Matrix Gla protein; Osteoarthritis; Guinea pig; Proteomics

资金

  1. Joint Program of Key Research and Development of Liaoning Province of China [2020JH2/10300138]
  2. Natural Science Foundation of Liaoning Province [20180530044]

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In this study, male Dunkin-Hartley guinea pigs were used to investigate the expression of Matrix Gla (gamma-carboxyglutamate) protein (MGP) throughout aging and disease pathogenesis. The results showed that MGP levels increased significantly with advancing age, and this may be linked to increased OA severity. Further studies are needed to confirm the association between MGP levels and OA severity.
Background Matrix Gla (gamma-carboxyglutamate) protein (MGP) is considered a strong inhibitor of ectopic calcification, and it has been associated with OA severity, although not conclusively. We utilized male Dunkin-Hartley (DH) guinea pigs to investigate the expression of MGP throughout aging and disease pathogenesis in a spontaneous model. Method Twenty-five male DH guinea pigs were obtained and nurtured to several timepoints, and then randomly and equally divided by age into five subgroups (1-, 3-, 6-, 9-, and 12-months, with the 1-month group as the reference group). DH guinea pigs in each group were euthanized at the designated month-age and the left or right medial tibial plateaus cartilages were randomly excised. OA severity was described by modified Mankin Score (MMS) at microscopy (Safranin O/Fast Green stain). Proteomic evaluation using isobaric tags for relative and absolute quantification (iTRAQ) was performed to validate the age-related changes in the MGP profiles, and immunohistochemistry (IHC) methods were applied for semi-quantitative determination of MGP expression in articular cartilage. Results The histopathologic findings validated the increasing severity of cartilage degeneration with age in the DH guinea pigs. The MMS showed significant, stepwise (every adjacent comparison P < 0.05) disease progression with month-age. The iTRAQ indicated that MGP levels increased significantly with advancing age (P < 0.05), as supported by the IHC result (P < 0.05). Conclusion Increased expression of MGP in male DH guinea pigs was present throughout aging and disease progression and may be link to increased OA severity. Further studies are needed to investigate and confirm the association between MGP levels and OA severity.

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