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巨噬细胞集落刺激因子、原癌基因c-Fms与破骨细胞及其前体细胞中的信号传导

M-CSF, c-Fms, and signaling in osteoclasts and their precursors.

作者信息

Ross F Patrick

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8118, St. Louis, MO 63110, USA.

出版信息

Ann N Y Acad Sci. 2006 Apr;1068:110-6. doi: 10.1196/annals.1346.014.

Abstract

Prevention of conditions, such as osteoporosis, requires an understanding of the molecular mechanisms of bone resorption. The understanding that cells of the myeloid lineage are osteoclast precursors suggests that macrophage colony-stimulating factor (M-CSF) plays an important role in osteoclast biology. Signals generated by the binding of M-CSF to the cell-surface receptor c-Fms appear to trigger events leading to osteoclast differentiation. We have created a chimeric variant of the c-Fms receptor, which has allowed study of downstream events activated by M-CSF in a model more relevant to normal physiology than prior studies, which have relied on myeloid tissues. Our studies suggest novel regulatory signaling pathways initiated via the c-Fms receptor.

摘要

预防诸如骨质疏松症等病症需要了解骨吸收的分子机制。认识到髓系谱系细胞是破骨细胞前体,这表明巨噬细胞集落刺激因子(M-CSF)在破骨细胞生物学中起重要作用。M-CSF与细胞表面受体c-Fms结合所产生的信号似乎触发了导致破骨细胞分化的事件。我们构建了一种c-Fms受体的嵌合变体,这使得在比以往依赖髓系组织的研究更符合正常生理学的模型中,能够研究由M-CSF激活的下游事件。我们的研究表明了通过c-Fms受体启动的新型调节信号通路。

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