Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN, United States; Indiana Center for Musculoskeletal Health, Indianapolis, IN, United States; Roudebush Veterans Administration Medical Center, Indianapolis, IN, United States.
Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN, United States; Indiana Center for Musculoskeletal Health, Indianapolis, IN, United States; Department of Biomedical and Applied Sciences, Indiana University School of Dentistry, Indianapolis, IN, United States.
Adv Protein Chem Struct Biol. 2019;116:237-281. doi: 10.1016/bs.apcsb.2019.01.002. Epub 2019 Feb 4.
The achievement of proper bone mass and architecture, and their maintenance throughout life requires the concerted actions of osteoblasts, the bone forming cells, and osteoclasts, the bone resorbing cells. The differentiation and activity of osteoblasts and osteoclasts are regulated by molecules produced by matrix-embedded osteocytes, as well as by cross talk between osteoblasts and osteoclasts through secreted factors. In addition, it is likely that direct contact between osteoblast and osteoclast precursors, and the contact of these cells with osteocytes and cells in the bone marrow, also modulates bone cell differentiation and function. With the advancement of molecular and genetic tools, our comprehension of the intracellular signals activated in bone cells has evolved significantly, from early suggestions that osteoblasts and osteoclasts have common precursors and that osteocytes are inert cells in the bone matrix, to the very sophisticated understanding of a network of receptors, ligands, intracellular kinases/phosphatases, transcription factors, and cell-specific genes that are known today. These advances have allowed the design and FDA-approval of new therapies to preserve and increase bone mass and strength in a wide variety of pathological conditions, improving bone health from early childhood to the elderly. We have summarized here the current knowledge on selected intracellular signal pathways activated in osteoblasts, osteocytes, and osteoclasts.
实现适当的骨量和骨结构,并在整个生命周期中维持这些结构,需要成骨细胞(骨形成细胞)和破骨细胞(骨吸收细胞)的协同作用。成骨细胞和破骨细胞的分化和活性受基质中嵌入的成骨细胞产生的分子以及成骨细胞和破骨细胞通过分泌因子进行的交流调节。此外,成骨细胞和破骨细胞前体细胞之间的直接接触,以及这些细胞与骨细胞和骨髓细胞的接触,也可能调节骨细胞的分化和功能。随着分子和遗传工具的进步,我们对骨细胞中激活的细胞内信号的理解已经有了显著的发展,从早期暗示成骨细胞和破骨细胞具有共同的前体细胞,以及骨细胞是骨基质中惰性细胞的观点,发展到今天对受体、配体、细胞内激酶/磷酸酶、转录因子和细胞特异性基因网络的复杂理解。这些进展使得设计和 FDA 批准新的治疗方法成为可能,以在各种病理情况下保留和增加骨量和骨强度,从而改善从儿童早期到老年的骨骼健康。我们在这里总结了目前关于成骨细胞、骨细胞和破骨细胞中激活的选定细胞内信号通路的知识。