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EXPRESSION OF BIOMARKERS OF OSTEOARTHRITIS IN MICE WITH AND WITHOUT RECEPTOR FOR ADVANCED GLYCATION END PRODUCTS (RAGE)
Author(s) -
Kartchner Jeffrey Zane,
Peterson D. M.,
Larkin D. J.,
Doxey A. S.,
Hollis W. R.,
Rees J. L.,
Ingersoll C.,
Jackson G. G.,
Wilhelm S. K.,
Haynie S. S.,
Seegmiller R. E.,
Stogdill J. A.,
Reynolds P. R.
Publication year - 2012
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.26.1_supplement.lb139
Subject(s) - rage (emotion) , glycation , downregulation and upregulation , osteoarthritis , medicine , cartilage , immunohistochemistry , matrix metalloproteinase , receptor , pathology , endocrinology , chemistry , anatomy , biology , neuroscience , biochemistry , gene , alternative medicine
HtrA1 and Mmp‐13 are reliable biomarkers of osteoarthritis (OA) and are upregulated at days post knee destabilization surgery (Polur et al., 2010). While expression of RAGE and its ligands are suggested, the exact mechanism for HtrA1 upregulation is not known (Cecil et al., 2005; Loeser et al., 2005). Our objective was to examine biomarkers of OA in the presence (control mice) and absence (RAGE knock‐out) of RAGE. We performed right knee destabilization and sham surgery on 8 week old control and RAGE knock‐out (KO) mice. We assayed for HtrA1, Mmp‐13, RAGE and S‐100 at 3, 7, 14 and 28 days post‐surgery by immunohistochemistry on both knee joints. We did not detect biomarkers of OA including Mmp‐13 in any sham surgery mice. In RAGE KO mice, we observed negligible staining of HtrA1 and faint staining of S‐100 at 28 days post‐surgery but not Mmp‐13. In contrast, we detected the presence of S‐100, HtrA1 and Mmp‐13 at focal points 3 days post‐surgery in control mice. By 28 days post‐surgery HtrA1 and Mmp‐13 expression is uniformly expressed in articular cartilage in control mice. RAGE KO does not entirely prevent HtrA1 upregulation but does protect against Mmp‐13 activation. Since the expression of Mmp‐13 is a terminal event resulting in OA, we conclude that RAGE KO protects against the most vital component of articular cartilage degradation and subsequently, OA.