Depletion of Annexin A5, Annexin A6, and Collagen X Causes No Gross Changes in Matrix Vesicle-Mediated Mineralization, but Lack of Collagen X Affects Hematopoiesis and the Th1/Th2 Response

被引:35
作者
Grskovic, Ivan [1 ]
Kutsch, Anna [1 ]
Frie, Christian [1 ]
Groma, Gergely [1 ]
Stermann, Jacek [1 ]
Schloetzer-Schrehardt, Ursula [2 ]
Niehoff, Anja [3 ]
Moss, Stephen E. [4 ]
Rosenbaum, Sabrina [1 ]
Poeschl, Ernst [5 ]
Chmielewski, Markus [6 ]
Rappl, Gunter [6 ]
Abken, Hinrich [6 ,7 ]
Bateman, John F. [8 ,9 ]
Cheah, Kathryn S. E. [10 ]
Paulsson, Mats [1 ,7 ,11 ]
Brachvogel, Bent [1 ,7 ]
机构
[1] Univ Cologne, Fac Med, Ctr Biochem, D-50931 Cologne, Germany
[2] Univ Erlangen Nurnberg, Dept Ophthalmol, Erlangen, Germany
[3] German Sport Univ Cologne, Inst Biomechan & Orthopaed, Cologne, Germany
[4] UCL, Inst Ophthalmol, Dept Cell Biol, London, England
[5] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[6] Univ Cologne, Fac Med, Dept Internal Med 1, D-50931 Cologne, Germany
[7] Univ Cologne, Fac Med, Ctr Mol Med Cologne CMMC, D-50931 Cologne, Germany
[8] Univ Melbourne, Murdoch Childrens Res Inst, Parkville, Vic 3052, Australia
[9] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic 3052, Australia
[10] Univ Hong Kong, Li Ka Shing Fac Med, Dept Biochem, Hong Kong, Hong Kong, Peoples R China
[11] Cologne Excellence Cluster Cellular Stress Respon, Cologne, Germany
关键词
ANNEXIN; COLLAGEN; MINERALIZATION; IN VIVO; ENDOCHONDRAL OSSIFICATION; HEMATOPOIESIS; GROWTH-PLATE CARTILAGE; IN-VITRO; ENDOCHONDRAL OSSIFICATION; OSTEOARTHRITIC CARTILAGE; EXTRACELLULAR-MATRIX; PERIVASCULAR CELLS; II COLLAGEN; NULL MICE; PHOSPHATIDYLSERINE; DIFFERENTIATION;
D O I
10.1002/jbmr.1682
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Numerous biochemical studies have pointed to an essential role of annexin A5 (AnxA5), annexin A6 (AnxA6), and collagen X in matrix vesicle-mediated biomineralization during endochondral ossification and in osteoarthritis. By binding to the extracellular matrix protein collagen X and matrix vesicles, annexins were proposed to anchor matrix vesicles in the extracellular space of hypertrophic chondrocytes to initiate the calcification of cartilage. However, mineralization appears to be normal in mice lacking AnxA5 and AnxA6, whereas collagen X-deficient mice show only subtle alterations in the growth plate organization. We hypothesized that the simultaneous lack of AnxA5, AnxA6, and collagen X in vivo induces more pronounced changes in the growth plate development and the initiation of mineralization. In this study, we generated and analyzed mice deficient for AnxA5, AnxA6, and collagen X. Surprisingly, mice were viable, fertile, and showed no obvious abnormalities. Assessment of growth plate development indicated that the hypertrophic zone was expanded in Col10a1(-/-) and AnxA5(-/-) AnxA6(-/-) Col10a1(-/-) newborns, whereas endochondral ossification and mineralization were not affected in 13-day- and 1-month-old mutants. In peripheral quantitative computed tomography, no changes in the degree of biomineralization were found in femora of 1-month- and 1-year-old mutants even though the diaphyseal circumference was reduced in Col10a1(-/-) and AnxA5(-/-) AnxA6(-/-) Col10a1(-/-) mice. The percentage of naive immature IgM(+)/IgM(+) B cells and peripheral T-helper cells were increased in Col10a1(-/)- and AnxA5(-/-) AnxA6(-/-) Col10a1(-/-) mutants, and activated splenic T cells isolated from Col10a1(-/-) mice secreted elevated levels of IL-4 and GM-CSF. Hence, collagen X is needed for hematopoiesis during endochondral ossification and for the immune response, but the interaction of annexin A5, annexin A6, and collagen X is not essential for physiological calcification of growth plate cartilage. Therefore, annexins and collagen X may rather fulfill functions in growth plate cartilage not directly linked to the mineralization process. (C) 2012 American Society for Bone and Mineral Research.
引用
收藏
页码:2399 / 2412
页数:14
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