Apoptosis and p53 expression in rat adjuvant arthritis

被引:38
作者
Tak, PP
Klapwijk, MS
Broersen, SF
van de Geest, DA
Overbeek, M
Firestein, GS
机构
[1] Acad Med Ctr, Dept Internal Med, Div Clin Immunol & Rheumatol, Amsterdam, Netherlands
[2] Univ Calif San Diego, Sch Med, Div Rheumatol, La Jolla, CA 92093 USA
关键词
adjuvant arthritis; apoptosis; p53; rheumatoid arthritis;
D O I
10.1186/ar92
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The kinetics of apoptosis and the apoptosis-regulating gene p53 in adjuvant arthritis (AA) were investigated to assess the value of the AA rat model for testing apoptosis-inducing therapies. Very few terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate (dUTP) nick end-labeling (TUNEL)-positive cells were detected during the early phases of AA, but on day 23 (chronic arthritis) the percentage of TUNEL-positive cells was significantly increased. Expression of p53 in synovial tissue gradually increased from days 5-23, which was markedly higher than p53 levels in rheumatoid arthritis (RA) synovium. Significant apoptosis only occurs late in rat AA and is concordant with marked p53 overexpression, making it a useful model for testing proapoptotic therapies, but rat AA is not the best model for p53 gene therapy because dramatic p53 overexpression occurs in the latter stages of the disease.
引用
收藏
页码:229 / 235
页数:7
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