Wang Z Q, Hemken P, Menton D, Gluck S
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
Am J Physiol. 1992 Aug;263(2 Pt 2):F277-83. doi: 10.1152/ajprenal.1992.263.2.F277.
Osteoclasts express high levels of a vacuolar H(+)-adenosinetriphosphatase (H(+)-ATPase) on the ruffled membrane which they employ to dissolve bone mineral by acidifying their site of attachment on bone. The factors that control amplification of H(+)-ATPase during osteoclast differentiation are poorly understood. We examined the expression of vacuolar H(+)-ATPase in a cell culture system in which mouse spleen cells can be induced to differentiate into osteoclasts by coculture with a mouse bone marrow stromal cell line. We found that the coculture system produced active osteoclasts, identified as multinucleated cells with staining for tartrate-resistant acid phosphatase activity that formed genuine resorption pits in bone. These cells developed high levels of H(+)-ATPase expression in culture, and omission of dexamethasone or 1 alpha,25-dihydroxyvitamin D3 from the coculture system each partially suppressed the expression of H(+)-ATPase. The results demonstrate that the spleen and PA6 cell coculture system may be useful for investigating the factors that control the induction of H(+)-ATPase amplification that occurs during osteoclast differentiation.
破骨细胞在皱褶膜上表达高水平的液泡型H⁺-腺苷三磷酸酶(H⁺-ATP酶),它们利用该酶通过酸化其在骨上的附着位点来溶解骨矿物质。在破骨细胞分化过程中控制H⁺-ATP酶扩增的因素尚不清楚。我们在一种细胞培养系统中检测了液泡型H⁺-ATP酶的表达,在该系统中,小鼠脾细胞与小鼠骨髓基质细胞系共培养时可被诱导分化为破骨细胞。我们发现该共培养系统产生了活性破骨细胞,这些细胞被鉴定为具有抗酒石酸酸性磷酸酶活性染色的多核细胞,它们在骨中形成了真正的吸收陷窝。这些细胞在培养中产生了高水平的H⁺-ATP酶表达,并且从共培养系统中省略地塞米松或1α,25-二羟基维生素D₃均部分抑制了H⁺-ATP酶的表达。结果表明,脾细胞与PA6细胞共培养系统可能有助于研究在破骨细胞分化过程中控制H⁺-ATP酶扩增诱导的因素。