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表达麻疹病毒核衣壳基因的破骨细胞呈现出畸形性骨炎表型。

Osteoclasts expressing the measles virus nucleocapsid gene display a pagetic phenotype.

作者信息

Kurihara N, Reddy S V, Menaa C, Anderson D, Roodman G D

机构信息

Department of Medicine/Hematology, University of Texas Health Science Center, San Antonio, Texas 78229, USA.

出版信息

J Clin Invest. 2000 Mar;105(5):607-14. doi: 10.1172/JCI8489.

Abstract

Osteoclasts (OCLs) in Paget's disease are markedly increased in number and size, have increased numbers of nuclei per multinucleated cell, and demonstrate increased resorption capacity and increased sensitivity to 1,25-(OH)(2)D(3), the active form of vitamin D. These cells also contain nuclear inclusions, reminiscent of those seen in paramyxovirus-infected cells, which cross-react with antibodies to measles virus nucleocapsid (MVNP) antigen. To elucidate the role of MV in the abnormal OCL phenotype of Paget's disease, we transduced normal OCL precursors with retroviral vectors expressing MVNP and the MV matrix (MVM) genes. The transduced cells were then cultured with 1,25-(OH)(2)D(3) for14 or 21 days to induce formation of OCL-like multinucleated cells. The MVNP-transduced cells formed increased numbers of multinucleated cells, which contained many more nuclei and had increased resorption capacity compared with multinucleated cells derived from empty vector-transduced (EV-transduced) and MVM-transduced or normal bone marrow cells. Furthermore, MVNP-transduced cells showed increased sensitivity to 1, 25-(OH)(2)D(3), and formed OCLs at concentrations of 1, 25-(OH)(2)D(3) that were 1 log lower than that required for normal, EV-transduced, or MVM-transduced cells. These results demonstrate that expression of the MVNP gene in normal OCL precursors stimulates OCL formation and induces OCLs that express a phenotype similar to that of pagetic OCLs. These results support a potential pathophysiologic role for MV infection in the abnormal OCL activity and morphology that are characteristic of pagetic OCLs.

摘要

佩吉特病中的破骨细胞数量和大小显著增加,每个多核细胞的细胞核数量增多,并且表现出吸收能力增强以及对维生素D的活性形式1,25-(OH)₂D₃的敏感性增加。这些细胞还含有核内包涵体,让人联想到在副粘病毒感染细胞中所见的核内包涵体,它们与抗麻疹病毒核衣壳(MVNP)抗原的抗体发生交叉反应。为了阐明麻疹病毒(MV)在佩吉特病异常破骨细胞表型中的作用,我们用表达MVNP和MV基质(MVM)基因的逆转录病毒载体转导正常破骨细胞前体。然后将转导后的细胞与1,25-(OH)₂D₃一起培养14或21天,以诱导形成破骨细胞样多核细胞。与来自空载体转导(EV转导)、MVM转导的细胞或正常骨髓细胞的多核细胞相比,MVNP转导的细胞形成的多核细胞数量增加,这些多核细胞含有更多的细胞核且吸收能力增强。此外,MVNP转导的细胞对1,25-(OH)₂D₃的敏感性增加,并且在1,25-(OH)₂D₃浓度比正常、EV转导或MVM转导细胞所需浓度低1个对数时就形成了破骨细胞。这些结果表明,正常破骨细胞前体中MVNP基因的表达刺激破骨细胞形成,并诱导出表达与佩吉特病破骨细胞相似表型的破骨细胞。这些结果支持MV感染在佩吉特病破骨细胞特征性的异常破骨细胞活性和形态中具有潜在的病理生理作用。

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