Bone Marrow Monocyte PECAM-1 Deficiency Elicits Increased Osteoclastogenesis Resulting in Trabecular Bone Loss

被引:17
作者
Wu, Yue [1 ]
Tworkoski, Kathryn [1 ]
Michaud, Michael [1 ]
Madri, Joseph A. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
关键词
PROTEIN-TYROSINE-PHOSPHATASE; ADHESION MOLECULE-1 PECAM-1; ADAPTER PROTEINS; PLATELET; CD31; POLYMORPHISM; REGULATOR; SHP-2; DIFFERENTIATION; IDENTIFICATION;
D O I
10.4049/jimmunol.0802398
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In our investigations of the bone marrow (BM) of PECAM-I null (knockout, KO) mice, we observed that the trabecular bone volume and number of trabeculae were significantly reduced in femural and tibial long bones. Further studies in vitro revealed increased numbers and size of osteoclasts, enhanced bone resorption on dentin substrates, and hypersensitivity to macrophage CSF and receptor activator of NF-kappa B ligand in BM-derived osteoclast precursor cultures from KO mice. Associations among PECAM-1, Syk, and SHP-1 were found in wild-type BM monocyte derived osteoclast-like cells. The absence of PECAM-1 and SHP-1 interactions in the KO cells leads to the dysregulation of Syk kinases and/or phosphatases, possibly SHP-1 Indeed, KO derived osteoclast-like cells exhibited increased Syk tyrosine phosphorylation levels compared with WT cells. Lastly, WT mice engrafted with marrow from KO kindred showed loss of trabecular bone analogous to KO mice, consistent with increased osteoclastogenesis. The Journal of Immunology, 2009, 182: 2672-2679.
引用
收藏
页码:2672 / 2679
页数:8
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