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Effects of major histocompatibility complex class II knockout on mouse mechanical properties during development

机译:主要组织相容性复合体II淘汰在发育过程中对小鼠机械性能的影响

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We investigated the effect of major histocompatibility complex class II (MHC II) knockout on the development of the mouse peripheral skeleton. These C2D mice had less skeletal development at 8, 12 and 16 weeks of age compared to wild-type C57BL/6J (B6) male mice. The C2D mice had decreased femur mechanical, geometric and compositional measurements compared to wild type mice at each of these ages. C2D femur stiffness (S), peak force in 3-pt bending (P{sub}m), and mineral mass (Min-M) were 74%, 64% and 66%, respectively, of corresponding B6 values at 8 weeks of age. Similar differences were measured at 12 weeks (for which C2D femoral S, P{sub}m and Min-M were 71%, 72% and 73%, respectively, of corresponding B6 values) and at 16 weeks (for which C2D femoral 5, P{sub}m and Min-M were 80%, 66% and 61%, respectively, of corresponding B6 values). MHC II knockout delays the development of adult bone properties and is accompanied by lower body mass compared to wild-type controls.
机译:我们研究了主要组织相容性复合物II(MHC II)敲除对小鼠周围骨架发育的影响。与野生型C57BL / 6J(B6)雄性小鼠相比,这些C2D小鼠的骨骼发育较少,12和16周。与这些年龄中的每一个的野生型小鼠相比,C2D小鼠的股骨机械,几何和组成测量减少。 C2D股骨刚度,3-Pt弯曲(P {} M)中的峰值和矿物质(Min-M)分别为74%,64%和66%,在8周的8周内分别为相应的B6值年龄。在12周(C2D股骨S,P {Sub} M和MIN-M分别为71%,72%和73%,相应的B6值)和16周(对于其中C2D股5的C2D,72%和73%)测量相似差异。 ,p {sub} m和min-m分别为相应的b6值80%,66%和61%)。 MHC II敲除延迟成人骨骼性质的发展,与野生型对照相比,伴有较低的体重。

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