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Histochemical aspects of the vascular invasion at the erosion zone of the epiphyseal cartilage in MMP-9-deficient mice

机译:MMP-9缺陷小鼠骨epi软骨侵蚀区血管侵犯的组织化学方面

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摘要

We have histologically examined vascular invasion and calcification of the hypertrophic zone during endochondral ossification in matrix metalloproteinase (MMP)-9 deficient (MMP-9~(-/-)) mice and in their littermates at 3 days, 3 weeks and 6 weeks after birth. Capillaries and osteoclasts at the chondro-osseous junction showed an intense MMP-9 immunopositivity, suggesting that they recognize chemical properties of cartilaginous matrices, and then release MMP-9 for cartilage degradation. CD31-positive capillaries and tartrate-resistant acid phosphatase-reactive osteoclasts could be found in the close proximity in the region of chondro-osseous junction in MMP-9~(-/-) mice, while in wild-type mice, vascular invasion preceded osteoclastic migration into the epiphyseal cartilage. Although MMP-9~(-/-) mice revealed larger hypertrophic zones, the index of calcified area was significantly smaller in MMP-9~(-/-) mice. Interestingly, the lower layer of the MMP-9~(-/-) hypertrophic zone showed intense MMP-13 staining, which could not be observed in wild-type mice. This indicates that MMP-13 may compensate for MMP-9 deficiency at that specific region, but not to a point at which the deficiency could be completely rescued. In conclusion, it seems that MMP-9 is the optimal enzyme for cartilage degradation during endochondral ossification by controlling vascular invasion and subsequent osteoclastic migration.
机译:我们已经组织学检查了基质金属蛋白酶(MMP)-9缺陷(MMP-9〜(-/-))小鼠及其同窝仔在3天,3周和6周后软骨内骨化过程中血管的浸润和肥大区的钙化出生。软骨-骨连接处的毛细血管和破骨细胞表现出强烈的MMP-9免疫阳性,表明它们识别软骨基质的化学性质,然后释放MMP-9进行软骨降解。在MMP-9〜(-/-)小鼠的软骨-骨连接区附近,可以发现CD31阳性的毛细血管和抗酒石酸的酸性破骨细胞,而在野生型小鼠中,血管侵入先于破骨细胞迁移到the软骨。尽管MMP-9〜(-/-)小鼠显示出较大的肥大区,但MMP-9〜(-/-)小鼠的钙化面积指数明显较小。有趣的是,MMP-9〜(-/-)肥大区的下层显示出强烈的MMP-13染色,这在野生型小鼠中无法观察到。这表明,MMP-13可以补偿该特定区域的MMP-9缺乏症,但不能完全弥补该缺乏症。总之,似乎MMP-9是软骨内骨化过程中通过控制血管入侵和随后的破骨细胞迁移而使软骨降解的最佳酶。

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