Teitelbaum Steven L, Ross F Patrick
Department of Pathology, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8118, St. Louis, Missouri 63110, USA.
Nat Rev Genet. 2003 Aug;4(8):638-49. doi: 10.1038/nrg1122.
Osteoclasts are the principal, if not exclusive, bone-resorbing cells, and their activity has a profound impact on skeletal health. So, disorders of skeletal insufficiency, such as osteoporosis, typically represent enhanced osteoclastic bone resorption relative to bone formation. Prevention of pathological bone loss therefore depends on an appreciation of the mechanisms by which osteoclasts differentiate from their precursors and degrade the skeleton. The past five years have witnessed important insights into osteoclast formation and function. Many of these discoveries have been made through genetic experiments that involved the rare hereditary disorder osteopetrosis.
破骨细胞是主要的(即便不是唯一的)骨吸收细胞,其活性对骨骼健康有着深远影响。因此,诸如骨质疏松症等骨骼功能不全的病症,通常表现为相对于骨形成而言,破骨细胞性骨吸收增强。所以,预防病理性骨质流失取决于对破骨细胞如何从其前体分化并破坏骨骼的机制的认识。在过去五年中,人们对破骨细胞的形成和功能有了重要的见解。其中许多发现是通过涉及罕见遗传性疾病骨石化症的基因实验取得的。