Kinesin-like protein CENP-E is upregulated in rheumatoid synovial fibroblasts

被引:15
作者
Kullmann, Frank [1 ]
Judex, Martin [1 ]
Ballhorn, Wibke [1 ]
Juesten, Hans-Peter [2 ]
Wessinghage, Dieter [2 ]
Welsh, John [3 ]
Yen, Tim J. [4 ]
Lang, Bernhard [1 ]
Hittle, Jim C. [4 ]
McClelland, Michael [3 ]
Gay, Steffen [5 ]
Schoelmerich, Juergen [1 ]
Mueller-Ladner, Ulf [1 ]
机构
[1] Univ Regensburg, Dept Internal Med 1, D-93042 Regensburg, Bavaria, Germany
[2] Univ Regensburg, Dept Orthoped, D-93042 Regensburg, Bavaria, Germany
[3] Sidney Kimmel Canc Ctr, San Diego, CA USA
[4] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[5] Univ Hosp, Ctr Expt Rheumatol, Dept Rheumatol, Zurich, Switzerland
关键词
arthritis; centromere; differential display; immunohistochemistry; in situ hybridization; RNA fingerprinting;
D O I
10.1186/ar13
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Our aim was to identify specifically expressed genes using RNA arbitrarily primed (RAP)polymerase chain reaction (PCR) for differential display in patients with rheumatoid arthritis (RA). In RA, amplification of a distinct PCR product suitable for sequencing could be observed. Sequence analysis identified the PCR product as highly homologous to a 434 base pair segment of the human centromere kinesin-like protein CENP-E. Differential expression of CENP-E was confirmed by quantitative reverse transcription PCR, immunohistochemistry and in situ hybridization. CENP-E expression was independent from prednisolone and could not be completely inhibited by serum starvation. RAP-PCR is a suitable method to identify differentially expressed genes in rheumatoid synovial fibroblasts. Also, because motifs of CENP-E show homologies to jun and fos oncogene products and are involved in virus assembly, CENP-E may be involved in the pathophysiology of RA.
引用
收藏
页码:71 / 80
页数:10
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