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缺乏核因子κB1和核因子κB2的小鼠中的骨质石化症

Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.

作者信息

Iotsova V, Caamaño J, Loy J, Yang Y, Lewin A, Bravo R

机构信息

Department of Oncology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000, USA.

出版信息

Nat Med. 1997 Nov;3(11):1285-9. doi: 10.1038/nm1197-1285.

Abstract

The nfkb1 and nfkb2 genes encode closely related products regulating immune and inflammatory responses. Their role during development and differentiation remains unclear. The generation of nfkb1 null mice (p50-/-) resulted in altered immune responses, but had no effect on development. Similarly, nfkb2 knockout mice (p52-/-) did not show developmental defects (J.C. et al., manuscript submitted). We have investigated the potential for in vivo compensatory functions of these genes by generating double-knockout mice. The surprising result was that the animals developed osteopetrosis because of a defect in osteoclast differentiation, suggesting redundant functions of NF-kappaB1 and NF-kappaB2 proteins in the development of this cell lineage. The osteopetrotic phenotype was rescued by bone marrow transplantation, indicating that the hematopoietic component was impaired. These results define a new mouse osteopetrotic mutant and implicate NF-kappaB proteins in bone development, raising new directions in the treatment of bone disorders.

摘要

nfkb1和nfkb2基因编码密切相关的产物,调节免疫和炎症反应。它们在发育和分化过程中的作用仍不清楚。nfkb1基因敲除小鼠(p50-/-)的产生导致免疫反应改变,但对发育没有影响。同样,nfkb2基因敲除小鼠(p52-/-)也未表现出发育缺陷(J.C.等人,已提交手稿)。我们通过生成双敲除小鼠研究了这些基因体内补偿功能的可能性。令人惊讶的结果是,这些动物由于破骨细胞分化缺陷而发生骨质石化,这表明NF-κB1和NF-κB2蛋白在该细胞谱系的发育中具有冗余功能。骨质石化表型通过骨髓移植得以挽救,表明造血成分受损。这些结果定义了一种新的小鼠骨质石化突变体,并表明NF-κB蛋白参与骨骼发育,为骨骼疾病的治疗提出了新的方向。

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