VEGF-A in Cardiomyocytes and Heart Diseases

被引:191
作者
Braile, Mariantonia [1 ,2 ,3 ]
Marcella, Simone [1 ,2 ,3 ]
Cristinziano, Leonardo [1 ,2 ,3 ]
Galdiero, Maria Rosaria [1 ,2 ,3 ,4 ]
Modestino, Luca [1 ,2 ,3 ]
Ferrara, Anne Lise [1 ,2 ,3 ,4 ]
Varricchi, Gilda [1 ,2 ,3 ,4 ]
Marone, Giancarlo [5 ,6 ]
Loffredo, Stefania [1 ,2 ,3 ,4 ]
机构
[1] Univ Naples Federico II, Dept Translat Med Sci, I-80131 Naples, Italy
[2] Univ Naples Federico II, Ctr Basic & Clin Immunol Res CISI, I-80131 Naples, Italy
[3] WAO Ctr Excellence, I-80131 Naples, Italy
[4] CNR Inst Expt Endocrinol & Oncol G Salvatore, I-80131 Naples, Italy
[5] Univ Naples Federico II, Dept Publ Hlth, I-80131 Naples, Italy
[6] Monaldi Hosp Pharm, Azienda Osped Osped Colli, I-80131 Naples, Italy
关键词
angiogenesis; atherosclerosis; cardiovascular disease; inflammation; ischemic heart disease; myocardial infarction; ENDOTHELIAL GROWTH-FACTOR; ACUTE MYOCARDIAL-INFARCTION; THERAPEUTIC ANGIOGENESIS; SIGNAL-TRANSDUCTION; CARDIAC MYOCYTE; GENE-THERAPY; MATRIX METALLOPROTEINASES; MOLECULAR-MECHANISMS; SUSTAINED DELIVERY; FACTOR EXPRESSION;
D O I
10.3390/ijms21155294
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The vascular endothelial growth factor (VEGF), a homodimeric vasoactive glycoprotein, is the key mediator of angiogenesis. Angiogenesis, the formation of new blood vessels, is responsible for a wide variety of physio/pathological processes, including cardiovascular diseases (CVD). Cardiomyocytes (CM), the main cell type present in the heart, are the source and target of VEGF-A and express its receptors, VEGFR1 and VEGFR2, on their cell surface. The relationship between VEGF-A and the heart is double-sided. On the one hand, VEGF-A activates CM, inducing morphogenesis, contractility and wound healing. On the other hand, VEGF-A is produced by CM during inflammation, mechanical stress and cytokine stimulation. Moreover, high concentrations of VEGF-A have been found in patients affected by different CVD, and are often correlated with an unfavorable prognosis and disease severity. In this review, we summarized the current knowledge about the expression and effects of VEGF-A on CM and the role of VEGF-A in CVD, which are the most important cause of disability and premature death worldwide. Based on clinical studies on angiogenesis therapy conducted to date, it is possible to think that the control of angiogenesis and VEGF-A can lead to better quality and span of life of patients with heart disease.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 200 条
[1]   VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis [J].
Abhinand, Chandran S. ;
Raju, Rajesh ;
Soumya, Sasikumar J. ;
Arya, Prabha S. ;
Sudhakaran, Perumana R. .
JOURNAL OF CELL COMMUNICATION AND SIGNALING, 2016, 10 (04) :347-354
[2]   Use of contact force sensing technology during radiofrequency ablation reduces recurrence of atrial fibrillation: A systematic review and meta-analysis [J].
Afzal, Muhammad R. ;
Chatta, Jawaria ;
Samanta, Anweshan ;
Waheed, Salman ;
Mahmoudi, Morteza ;
Vukas, Rachel ;
Gunda, Sampath ;
Reddy, Madhu ;
Dawn, Buddhadeb ;
Lakkireddy, Dhanunjaya .
HEART RHYTHM, 2015, 12 (09) :1990-1996
[3]   The Angiogenic Factor Secretoneurin Induces Coronary Angiogenesis in a Model of Myocardial Infarction by Stimulation of Vascular Endothelial Growth Factor Signaling in Endothelial Cells [J].
Albrecht-Schgoer, Karin ;
Schgoer, Wilfried ;
Holfeld, Johannes ;
Theurl, Markus ;
Wiedemann, Dominik ;
Steger, Christina ;
Gupta, Rajesh ;
Semsroth, Severin ;
Fischer-Colbrie, Reiner ;
Beer, Arno G. E. ;
Stanzl, Ursula ;
Huber, Eva ;
Misener, Sol ;
Dejaco, Daniel ;
Kishore, Raj ;
Pachinger, Otmar ;
Grimm, Michael ;
Bonaros, Nikolaos ;
Kirchmair, Rudolf .
CIRCULATION, 2012, 126 (21) :2491-+
[4]   THE CONCISE GUIDE TO PHARMACOLOGY 2015/16: Catalytic receptors [J].
Alexander, Stephen P. H. ;
Fabbro, Doriano ;
Kelly, Eamonn ;
Marrion, Neil ;
Peters, John A. ;
Benson, Helen E. ;
Faccenda, Elena ;
Pawson, Adam J. ;
Sharman, Joanna L. ;
Southan, Christopher ;
Davies, Jamie A. ;
Aldrich, R. ;
Attali, B. ;
Back, M. ;
Barnes, N. M. ;
Bathgate, R. ;
Beart, P. M. ;
Becirovic, E. ;
Biel, M. ;
Birdsall, N. J. ;
Boison, D. ;
Brauner-Osborne, H. ;
Broeer, S. ;
Bryant, C. ;
Burnstock, G. ;
Burris, T. ;
Cain, D. ;
Calo, G. ;
Chan, S. L. ;
Chandy, K. G. ;
Chiang, N. ;
Christakos, S. ;
Christopoulos, A. ;
Chun, J. J. ;
Chung, J. -J. ;
Clapham, D. E. ;
Connor, M. A. ;
Coons, L. ;
Cox, H. M. ;
Dautzenberg, F. M. ;
Dent, G. ;
Douglas, S. D. ;
Dubocovich, M. L. ;
Edwards, D. P. ;
Farndale, R. ;
Fong, T. M. ;
Forrest, D. ;
Fowler, C. J. ;
Fuller, P. ;
Gainetdinov, R. R. .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (24) :5979-6023
[5]   Secretion of IL-6, IL-11 and LIF by human cardiomyocytes in primary culture [J].
Ancey, C ;
Corbi, P ;
Froger, J ;
Delwail, A ;
Wijdenes, J ;
Gascan, H ;
Potreau, D ;
Lecron, JC .
CYTOKINE, 2002, 18 (04) :199-205
[6]   Vascular Endothelial Growth Factor-Angiopoietin Chimera With Improved Properties for Therapeutic Angiogenesis [J].
Anisimov, Andrey ;
Tvorogov, Denis ;
Alitalo, Annamari ;
Leppanen, Veli-Matti ;
An, Yuri ;
Han, Eun Chun ;
Orsenigo, Fabrizio ;
Gaal, Emilia Ilona ;
Holopainen, Tanja ;
Koh, Young Jun ;
Tammela, Tuomas ;
Korpisalo, Petra ;
Keskitalo, Salla ;
Jeltsch, Michael ;
Yla-Herttuala, Seppo ;
Dejana, Elisabetta ;
Koh, Gou Young ;
Choi, Chulhee ;
Saharinen, Pipsa ;
Alitalo, Kari .
CIRCULATION, 2013, 127 (04) :424-+
[7]  
Aoyagi T., 2012, J CELL SCI R, Vs5, DOI [DOI 10.4172/2157-7013, 10.4172/2157-7013.S5-003]
[8]  
Arrillaga-Romany Isabel, 2014, CNS Oncol, V3, P349, DOI 10.2217/cns.14.31
[9]   Induction of functional neovascularization by combined VEGF and angiopoietin-1 gene transfer using AAV vectors [J].
Arsic, N ;
Zentilin, L ;
Zacchigna, S ;
Santoro, D ;
Stanta, G ;
Salvi, A ;
Sinagra, G ;
Giacca, M .
MOLECULAR THERAPY, 2003, 7 (04) :450-459
[10]   Accelerated restitution of endothelial integrity and endothelium-dependent function after phVEGF(165) gene transfer [J].
Asahara, T ;
Chen, DH ;
Tsurumi, Y ;
Kearney, M ;
Rossow, S ;
Passeri, J ;
Symes, JF ;
Isner, JM .
CIRCULATION, 1996, 94 (12) :3291-3302