The Ets 1 transcription factor is upregulated during inflammatory angiogenesis in rheumatoid arthritis

被引:23
作者
Wernert, N
Justen, HP
Rothe, M
Behrens, P
Dreschers, S
Neuhaus, T
Florin, A
Sachinidis, A
Vetter, H
Ko, Y
机构
[1] Univ Bonn, Inst Pathol, D-53011 Bonn, Germany
[2] Univ Regensburg, Clin Orthoped, Bavarian Red Cross Hosp Rheumat Dis, Bad Abbach, Germany
[3] Univ Bonn, Med Poliklin, D-53111 Bonn, Germany
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2002年 / 80卷 / 04期
关键词
Ets; 1; arthritis; real-time PCR; in situ hybridization; immunohistochemistry;
D O I
10.1007/s00109-001-0316-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neovascularization of the inflamed synovium and pannus is one of the hallmarks of chronic rheumatoid arthritis. It contributes to disease progression by supplying blood to the inflamed tissues and by recruiting immune competent and inflammatory cells. Angiogenesis is tightly regulated at several levels, but of significant importance is transcription. The Ets 1 transcription factor has been intimately linked to the regulation of angiogenesis under both physiological and pathological conditions and is induced in endothelial cells by vascular endothelial growth factor, the most important angiogenic factor in rheumatoid arthritis. We investigated Ets 1 expression in synovial membranes of joints in patients with active rheumatoid arthritis and compared the results to those obtained in patients with degenerative joint disease, which is characterized by significantly less neoangiogenesis. Using quantitative densitometric and real-time RT-PCR approaches, we found a significant upregulation of Ets 1 transcripts in rheumatic, compared to osteoarthritic, synovial membranes. Moreover, we were able to attribute both Ets 1 mRNA and Ets 1 protein to capillary endothelial cells of newly formed blood vessels by in situ hybridization and immunohistochemistry. Finally, our data suggest important roles of the Ets 1 transcription factor in the regulation of inflammatory angiogenesis in rheumatoid arthritis.
引用
收藏
页码:258 / 266
页数:9
相关论文
共 49 条
[1]   12-O-TETRADECANOYL-PHORBOL-13-ACETATE INDUCTION OF THE HUMAN COLLAGENASE GENE IS MEDIATED BY AN INDUCIBLE ENHANCER ELEMENT LOCATED IN THE 5'-FLANKING REGION [J].
ANGEL, P ;
BAUMANN, I ;
STEIN, B ;
DELIUS, H ;
RAHMSDORF, HJ ;
HERRLICH, P .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (06) :2256-2266
[2]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]   New vessels, new approaches: angiogenesis as a therapeutic target in musculoskeletal disorders [J].
Ballara, SC ;
Miotla, JM ;
Paleolog, EM .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 1999, 80 (05) :235-250
[4]  
Berse B, 1999, CLIN EXP IMMUNOL, V115, P176
[5]  
Bièche I, 1999, CANCER RES, V59, P2759
[6]   Antiangiogenic therapy of experimental cancer does not induce acquired drug resistance [J].
Boehm, T ;
Folkman, J ;
Browder, T ;
OReilly, MS .
NATURE, 1997, 390 (6658) :404-407
[7]   VEGF gene therapy: stimulating angiogenesis or angioma-genesis? [J].
Carmeliet, P .
NATURE MEDICINE, 2000, 6 (10) :1102-1103
[8]   Insights in vessel development and vascular disorders using targeted inactivation and transfer of vascular endothelial growth factor, the tissue factor receptor, and the plasminogen system [J].
Carmeliet, P ;
Moons, L ;
Dewerchin, M ;
Mackman, N ;
Luther, T ;
Breier, G ;
Ploplis, V ;
Muller, M ;
Nagy, A ;
Plow, E ;
Gerard, R ;
Edgington, T ;
Risau, W ;
Collen, D .
ATHEROSCLEROSIS IV: RECENT ADVANCES IN ATHEROSCLEROSIS RESEARCH: THE FOURTH SARATOGA INTERNATIONAL CONFERENCE ON ATHEROSCLEROSIS, 1997, 811 :191-206
[9]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[10]   Ets transcription factors and human disease [J].
Dittmer, J ;
Nordheim, A .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1998, 1377 (02) :F1-F11