Transcription factor SOX18 is expressed in human coronary atherosclerotic lesions and regulates DNA synthesis and vascular cell growth

被引:46
作者
García-Ramírez, M [1 ]
Martínez-González, J [1 ]
Juan-Babot, JO [1 ]
Rodríguez, C [1 ]
Badimon, L [1 ]
机构
[1] Hosp Santa Creui & Sant Pau, Ctr Invest Cardiovasc, CSIC ICCC, Barcelona 08025, Spain
关键词
vascular biology; gene expression; endothelial function; atherosclerosis; growth factors; SOX18;
D O I
10.1161/01.ATV.0000187464.81959.23
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-SOX18, a member of the SOX gene family (SRY-like 3-hydroxy-3-methylglutaryl box gene), is a transcription factor expressed in the development of blood vessels during embryogenesis. We analyzed SOX18 expression in human coronary atherosclerotic lesions and investigated its potential function in vascular cells. Methods and Results-In advanced human coronary atherosclerotic lesions, SOX18 immunostaining was localized in endothelial cells (on the luminal surface, in vasa vasorum, and in intimal neovessels) and in vascular smooth muscle cells (VSMCs) scattered in the intima, colocalizing with proliferating cell nuclear antigen. In cell cultures, SOX18 was mainly localized in subconfluent and denuded areas. Significant SOX18 mRNA levels (by Northern blot analysis and reverse transcription-polymerase chain reaction) were detected in cell cultures from human umbilical vein endothelial cells and human VSMCs. Antisense SOX18 inhibited DNA synthesis ([H-3] thymidine incorporation) and vascular cell growth. Antisense SOX18 also significantly reduced VSMC regrowth after injury in an in vitro model of wound repair. Conclusions-Our results indicate that SOX18 is involved in vascular cell growth and suggest that this transcription factor may play a role in atherosclerosis.
引用
收藏
页码:2398 / 2403
页数:6
相关论文
共 37 条
[11]   Cloning and functional analysis of the Sry-related HMG box gene, Sox18 [J].
Hosking, BM ;
Wyeth, JR ;
Pennisi, DJ ;
Wang, SCM ;
Koopman, P ;
Muscat, GEO .
GENE, 2001, 262 (1-2) :239-247
[12]   VASCULAR CELL-ADHESION MOLECULE-1 - CONTRASTING TRANSCRIPTIONAL CONTROL MECHANISMS IN MUSCLE AND ENDOTHELIUM [J].
IADEMARCO, MF ;
MCQUILLAN, JJ ;
DEAN, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) :3943-3947
[13]   Patterns of vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression in rabbit and mouse atherosclerotic lesions and at sites predisposed to lesion formation [J].
Iiyama, K ;
Hajra, L ;
Iiyama, M ;
Li, HM ;
DiChiara, M ;
Medoff, BD ;
Cybulsky, MI .
CIRCULATION RESEARCH, 1999, 85 (02) :199-207
[14]   Vascular endothelial growth factor (VEGF) expression in human coronary atherosclerotic lesions - Possible pathophysiological significance of VEGF in progression of atherosclerosis [J].
Inoue, M ;
Itoh, H ;
Ueda, M ;
Naruko, T ;
Kojima, A ;
Komatsu, R ;
Doi, K ;
Ogawa, Y ;
Tamura, N ;
Takaya, K ;
Igaki, T ;
Yamashita, J ;
Chun, TH ;
Masatsugu, K ;
Becker, AE ;
Nakao, K .
CIRCULATION, 1998, 98 (20) :2108-2116
[15]   Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia [J].
Irrthum, A ;
Devriendt, K ;
Chitayat, D ;
Matthijs, G ;
Glade, C ;
Steijlen, PM ;
Fryns, JP ;
Van Steensel, MAM ;
Vikkula, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (06) :1470-1478
[16]   Sox18 mutations in the ragged mouse alleles ragged-like and opossum [J].
James, K ;
Hosking, B ;
Gardner, J ;
Muscat, GEO ;
Koopman, P .
GENESIS, 2003, 36 (01) :1-6
[17]   Pairing SOX off with partners in the regulation of embryonic development [J].
Kamachi, Y ;
Uchikawa, M ;
Kondoh, H .
TRENDS IN GENETICS, 2000, 16 (04) :182-187
[18]  
Katsuda Shogo, 2003, J Atheroscler Thromb, V10, P267
[19]   Regulation of cell migration in atherosclerosis. [J].
Kraemer R. .
Current Atherosclerosis Reports, 2000, 2 (5) :445-452
[20]   Atherosclerosis [J].
Lusis, AJ .
NATURE, 2000, 407 (6801) :233-241