Evidence of somatic mutations in osteoarthritis

被引:27
作者
Mertens, F
Palsson, E
Lindstrand, A
ToksvigLarsen, S
Knuutila, S
Larramendy, ML
ElRifai, W
Limon, J
Mitelman, F
Mandahl, N
机构
[1] UNIV LUND HOSP,DEPT ORTHOPED,S-22185 LUND,SWEDEN
[2] UNIV HELSINKI,HAARTMAN INST,DEPT MED GENET,FIN-00014 HELSINKI,FINLAND
[3] MED UNIV GDANSK,DEPT BIOL & GENET,GDANSK,POLAND
关键词
D O I
10.1007/s004390050278
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We examined, cytogenetically and by in situ hybridization (ISH) techniques, the synovia, osteophytes, and articular cartilage from 32 patients with pronounced osteoarthritis (OA), a prevalent form of arthropathy characterized by progressive reduction of articular cartilage, and synovial samples from 17 control patients. In short-term cultures, clonal chromosome aberrations, in particular the gain of chromosomes 7 (+7) and 5 (+5), were found to be strongly associated with OA. These aberrations were found in almost 90% of the cultures from synovia and osteophytes, whereas only 1/11 synovial samples from joints unequivocally unaffected by OA had cells with +5 or +7. The in vivo nature of trisomy 7 was demonstrated by ISH on uncultured cells, and serial passaging showed that cells with +7 had a proliferative advantage in vitro. Thus, the combined data indicate that cells with somatic mutations appear early and may be influential in the disease process leading to OA.
引用
收藏
页码:651 / 656
页数:6
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