BMP signaling in vascular diseases

被引:252
作者
Cai, Jie [1 ,2 ]
Pardali, Evangelia [3 ]
Sanchez-Duffhues, Gonzalo [1 ,2 ]
ten Dijke, Peter [1 ,2 ]
机构
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Ctr Biomed Genet, NL-2300 RC Leiden, Netherlands
[3] Univ Hosp Munster, Dept Cardiol & Angiol, Munster, Germany
关键词
BMP signaling; Cardiovascular disease; Pulmonary arterial hypertension; Hereditary hemorrhagic telangiectasia; Vascular calcification; Tumor angiogenesis; BONE MORPHOGENETIC PROTEIN; MATRIX GLA PROTEIN; HEREDITARY HEMORRHAGIC TELANGIECTASIA; PLURIPOTENT STEM-CELLS; GROWTH-FACTOR-BETA; PRIMARY PULMONARY-HYPERTENSION; SMOOTH-MUSCLE-CELLS; FUNCTIONAL-ANALYSIS; ARTERY SMOOTH; TUMOR-GROWTH;
D O I
10.1016/j.febslet.2012.04.030
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
Bone morphogenetic proteins (BMPs) are members of the transforming growth factor-beta (TGF-beta) family that signal via type I and type II serine/threonine kinase receptors and intracellular Smad transcription factors. BMPs are multifunctional regulators of development and tissue homeostasis and they were initially characterized as inducers of bone regeneration. Genetic studies in humans and mice showed that perturbations in BMP signaling lead to various diseases, such as skeletal diseases, vascular diseases and cancer. Mutations in BMP type II receptor and BMP type I receptor/activin receptor-like kinase 1 have been linked to pulmonary arterial hypertension and hereditary hemorrhagic telangiectasia, respectively. BMPs have also been implicated in promoting vascular calcification and tumor angiogenesis. In this review we discuss the role of BMP signaling in vascular diseases and the value of BMP signaling as a vascular disease marker or a therapeutic target. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1993 / 2002
页数:10
相关论文
共 178 条
[81]   Altered Transforming Growth Factor-Beta Signaling in a Murine Model of Thoracic Aortic Aneurysm [J].
Jones, Jeffrey A. ;
Barbour, John R. ;
Stroud, Robert E. ;
Bouges, Shenikqua ;
Stephens, Shelly L. ;
Spinale, Francis G. ;
Ikonomidis, John S. .
JOURNAL OF VASCULAR RESEARCH, 2008, 45 (06) :457-468
[82]   Signal transduction by bone morphogenetic proteins [J].
Kawabata, M ;
Imamura, T ;
Miyazono, K .
CYTOKINE & GROWTH FACTOR REVIEWS, 1998, 9 (01) :49-61
[83]   Bone morphogenetic proteins signal through the transforming growth factor-β type III receptor [J].
Kirkbride, Kellye C. ;
Townsend, Todd A. ;
Bruinsma, Monique W. ;
Barnett, Joey V. ;
Blobe, Gerard C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (12) :7628-7637
[84]  
Kiyozuka Y, 2001, ANTICANCER RES, V21, P1723
[85]   Bone morphogenetic protein 2 exerts diverse effects on cell growth in vitro and is expressed in human pancreatic cancer in vivo [J].
Kleeff, J ;
Maruyama, H ;
Ishiwata, T ;
Sawhney, H ;
Friess, H ;
Büchler, MW ;
Korc, M .
GASTROENTEROLOGY, 1999, 116 (05) :1202-1216
[86]  
Kozawa O, 2001, J CELL BIOCHEM, V81, P430, DOI 10.1002/1097-4644(20010601)81:3<430::AID-JCB1056>3.0.CO
[87]  
2-G
[88]   Human circulating CD14+ monocytes as a source of progenitors that exhibit mesenchymal cell differentiation [J].
Kuwana, M ;
Okazaki, Y ;
Kodama, H ;
Izumi, K ;
Yasuoka, H ;
Ogawa, Y ;
Kawakami, Y ;
Ikeda, Y .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 74 (05) :833-845
[89]   Essential role of endothelial Smad4 in vascular remodeling and integrity [J].
Lan, Yu ;
Liu, Bing ;
Yao, Huiyu ;
Li, Fangfei ;
Weng, Tujun ;
Yang, Guan ;
Li, Wenlong ;
Cheng, Xuan ;
Mao, Ning ;
Yang, Xiao .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (21) :7683-7692
[90]   Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension [J].
Lane, KB ;
Machado, RD ;
Pauciulo, MW ;
Thomson, JR ;
Phillips, JA ;
Loyd, JE ;
Nichols, WC ;
Trembath, RC .
NATURE GENETICS, 2000, 26 (01) :81-84