Mimura H, Cao X, Ross F P, Chiba M, Teitelbaum S L
Department of Pathology and Laboratory Medicine, Jewish Hospital at Washington University Medical Center, St. Louis, Missouri 63110.
Endocrinology. 1994 Mar;134(3):1061-6. doi: 10.1210/endo.134.3.8119143.
Osteoclasts are polykaryons and the principal, if not exclusive, resorptive cell of bone. They are members of the monocyte/macrophage family whose precursors differentiate under the influence of 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3]. Bone resorption is dependent on osteoclast-bone attachment, and we have shown that the integrin alpha v beta 3 is critical to the resorptive process. Thus, we asked whether 1,25-(OH)2D3 enhances the expression of alpha v beta 3 on the surface of osteoclast precursors and if the steroid modulates expression of the beta 3-integrin subunit. We found that 1,25-(OH)2D3 promotes the plasma membrane appearance of alpha v beta 3 on avian bone marrow-derived osteoclast precursors and does so at physiological concentrations (10(-11) M) of the steroid. The effect is time dependent, appearing within 1 day of treatment. A full-length avian cDNA was cloned to explore the molecular mechanisms of beta 3 expression. The deduced amino acid sequence of the cDNA is 81% identical and 89% similar to that of human beta 3. Northern analysis demonstrates that beta 3 mRNA levels in vitamin D-treated osteoclast precursors mirror protein expression. Nuclear run-on experiments document the transcriptional nature of the event.
破骨细胞是多核细胞,是骨组织主要的(即便不是唯一的)吸收细胞。它们是单核细胞/巨噬细胞家族的成员,其前体在1,25 - 二羟基维生素D3 [1,25-(OH)2D3]的影响下分化。骨吸收依赖于破骨细胞与骨的附着,并且我们已经表明整合素αvβ3对吸收过程至关重要。因此,我们询问1,25-(OH)2D3是否会增强破骨细胞前体表面αvβ3的表达,以及该类固醇是否会调节β3整合素亚基的表达。我们发现1,25-(OH)2D3可促进αvβ3在源自鸡骨髓的破骨细胞前体的质膜上出现,并且在该类固醇的生理浓度(10^(-11) M)下即可做到。该作用具有时间依赖性,在处理后1天内出现。克隆了一个全长鸡cDNA以探究β3表达的分子机制。该cDNA推导的氨基酸序列与人类β3的氨基酸序列有81%的同一性和89%的相似性。Northern分析表明,经维生素D处理的破骨细胞前体中β3 mRNA水平反映了蛋白质表达情况。核转录实验证明了该事件的转录性质。