Enhanced RANK ligand expression and responsivity of bone marrow cells in Paget's disease of bone

被引:117
作者
Menaa, C
Reddy, SV
Kurihata, N
Maeda, H
Anderson, D
Cundy, T
Cornish, J
Singer, FR
Bruder, JM
Roodman, GD
机构
[1] Audie L Murphy Adm Vet Hosp, San Antonio, TX 78284 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Med Hematol, San Antonio, TX USA
[3] Immunex Res & Dev Corp, Seattle, WA 98101 USA
[4] Univ Auckland, Auckland 1, New Zealand
[5] John Wayne Canc Ctr, Santa Monica, CA USA
关键词
D O I
10.1172/JCI9133
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Paget's disease is characterized by highly localized areas of increased osteoclast (OCL) activity. This suggests that the microenvironment in pagetic lesions is highly osteoclastogenic, or that OCL precursors in these lesions are hyperresponsive to osteoclastogenic factors (or both). To examine these possibilities, me compared RANK ligand (RANKL) mRNA expression in a marrow stromal cell line developed from a pagetic lesion (PSV10) with that in a normal stromal cell line (Saka), and expression in marrow samples from affected bones of Paget's patients with that in normal marrow. RANKL mRNA was increased in PSV10 cells and pagetic marrow compared with Saka cells and normal marrow, and was also increased in marrow from affected bones compared with uninvolved bones from Paget's patients. Furthermore, pagetic marrow cells formed OCLs at much lower RANKL, concentrations than did normal marrow. Anti-IL-6 decreased the RANKL responsivity of pagetic marrow to normal levels, whereas addition of IL-6 to normal marrow enhanced RANKL responsivity. Thus, RANKL expression and responsivity is increased in pagetic lesions, in part mediated by IL-6. These data suggest that the combination of enhanced expression of RANKL in affected bones and increased RANKL sensitivity of pagetic OCL precursors may contribute to the elevated numbers of OCLs in Paget's disease.
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页码:1833 / 1838
页数:6
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