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Altered endochondral ossification in collagen X mouse models leads to impaired immune responses
Author(s) -
Sweeney E.,
Campbell M.,
Watkins K.,
Hunter C.A.,
Jacenko O.
Publication year - 2008
Publication title -
developmental dynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.634
H-Index - 141
eISSN - 1097-0177
pISSN - 1058-8388
DOI - 10.1002/dvdy.21594
Subject(s) - biology , endochondral ossification , immune system , haematopoiesis , cd8 , splenocyte , bone marrow , immunology , microbiology and biotechnology , cartilage , endocrinology , medicine , stem cell , anatomy
Disruption of collagen X function in hypertrophic cartilage undergoing endochondral ossification was previously linked to altered hematopoiesis in collagen X transgenic (Tg) and null (KO) mice (Jacenko et al., [2002] Am J Pathol 160:2019–2034). Mice displayed altered growth plates, diminished trabecular bone, and marrow hypoplasia with an aberrant lymphocyte profile throughout life. This study identifies altered B220 + , CD4 + , and CD8 + lymphocyte numbers, as well as CD4 + /fox3P + T regulatory cells in the collagen X mice. Additionally, diminished in vitro splenocyte responses to mitogens and an inability of mice to survive a challenge with Toxoplasma gondii , confirm impaired immune responses. In concert, ELISA and protein arrays identify aberrant levels of inflammatory, chemo‐attractant, and matrix binding cytokines in collagen X mouse sera. These data link the disruption of collagen X function in the chondro‐osseous junction to an altered hematopoietic stem cell niche in the marrow, resulting in impaired immune function. Developmental Dynamics 237:2693–2704, 2008. © 2008 Wiley‐Liss, Inc.