School of Dentistry, University of Missouri-Kansas City, Kansas City, MO 64108-2784, USA.
J Bone Miner Res. 2012 May;27(5):1018-29. doi: 10.1002/jbmr.1567.
Osteoclasts are thought to be solely responsible for the removal of bone matrix. However, we show here that osteocytes can also remove bone matrix by reversibly remodeling their perilacunar/canalicular matrix during the reproductive cycle. In contrast, no osteocytic remodeling was observed with experimental unloading despite similar degrees of bone loss. Gene array analysis of osteocytes from lactating animals revealed an elevation of genes known to be utilized by osteoclasts to remove bone, including tartrate-resistant acid phosphatase (TRAP) and cathepsin K, that returned to virgin levels upon weaning. Infusion of parathyroid hormone-related peptide (PTHrP), known to be elevated during lactation, induced TRAP activity and cathepsin K expression in osteocytes concurrent with osteocytic remodeling. Conversely, animals lacking the parathyroid hormone type 1 receptor (PTHR1) in osteocytes failed to express TRAP or cathepsin K or to remodel their osteocyte perilacunar matrix during lactation. These studies show that osteocytes remove mineralized matrix through molecular mechanisms similar to those utilized by osteoclasts.
破骨细胞被认为是唯一负责去除骨基质的细胞。然而,我们在这里表明,成骨细胞也可以通过在生殖周期中可逆地重塑其骨陷窝/管腔基质来去除骨基质。相比之下,尽管有类似程度的骨丢失,实验性去负荷时未观察到成骨细胞重塑。对哺乳期动物成骨细胞的基因阵列分析显示,一些已知被破骨细胞用于去除骨的基因(包括抗酒石酸酸性磷酸酶(TRAP)和组织蛋白酶 K)的表达水平升高,在断奶后恢复到未孕水平。甲状旁腺激素相关肽(PTHrP)的输注,已知在哺乳期升高,可诱导成骨细胞中的 TRAP 活性和组织蛋白酶 K 表达,同时伴随成骨细胞重塑。相反,成骨细胞中缺乏甲状旁腺激素 1 型受体(PTHR1)的动物在哺乳期未能表达 TRAP 或组织蛋白酶 K,也未能重塑其成骨细胞骨陷窝基质。这些研究表明,成骨细胞通过与破骨细胞相似的分子机制去除矿化基质。