4.7 Article

Dysregulation of Local Stem/Progenitor Cells as a Common Cellular Mechanism for Heterotopic Ossification

期刊

STEM CELLS
卷 27, 期 1, 页码 150-156

出版社

WILEY
DOI: 10.1634/stemcells.2008-0576

关键词

Heterotopic ossification; Fibrodysplasia ossificans progressiva; Nse-BMP4; Macrophages

资金

  1. Center for Research in FOP
  2. Related Disorders of The University of Pennsylvania School of Medicine
  3. NIH [NS20013, NS20778]
  4. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS020778, R01NS020013] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Heterotopic ossification (HO), the abnormal formation of true marrow-containing bone within extraskeletal soft tissues, is a serious bony disorder that may be either acquired or hereditary. We utilized an animal model of the genetic disorder fibrodysplasia ossificans progressiva to examine the cellular mechanisms underlying HO. We found that HO in these animals was triggered by soft tissue injuries and that the effects were mediated by macrophages. Spreading of HO beyond the initial injury site was mediated by an abnormal adaptive immune system. These observations suggest that dysregulation of local stem/progenitor cells could be a common cellular mechanism for typical HO irrespective of the signal initiating the bone formation. STEM CELLS 2009; 27: 150-156

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