A Role for Partial Endothelial-Mesenchymal Transitions in Angiogenesis?

被引:161
作者
Welch-Reardon, Katrina M. [1 ]
Wu, Nan [1 ]
Hughes, Christopher C. W. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Edwards Lifesci Ctr Adv Cardiovasc Technol, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
angiogenesis; EMT; endothelial; transcription factor; GROWTH-FACTOR-BETA; TGF-BETA; CARDIAC FIBROSIS; VALVE DEVELOPMENT; KIDNEY FIBROSIS; BHLH FACTORS; E-CADHERIN; IN-VITRO; NOTCH; CELLS;
D O I
10.1161/ATVBAHA.114.303220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The contribution of epithelial-to-mesenchymal transitions (EMT) in both developmental and pathological conditions has been widely recognized and studied. In a parallel process, governed by a similar set of signaling and transcription factors, endothelial-to-mesenchymal transitions (EndoMT) contribute to heart valve formation and the generation of cancer-associated fibroblasts. During angiogenic sprouting, endothelial cells express many of the same genes and break down basement membrane; however, they retain intercellular junctions and migrate as a connected train of cells rather than as individual cells. This has been termed a partial endothelial-to-mesenchymal transition. A key regulatory check-point determines whether cells undergo a full or a partial epithelial-to-mesenchymal transitions/endothelial-to-mesenchymal transition; however, very little is known about how this switch is controlled. Here we discuss these developmental/pathological pathways, with a particular focus on their role in vascular biology.
引用
收藏
页码:303 / 308
页数:6
相关论文
共 66 条
[21]   Endothelial Cells Recruit Macrophages and Contribute to a Fibrotic Milieu in Bleomycin Lung Injury [J].
Leach, Heather G. ;
Chrobak, Izabela ;
Han, Rong ;
Trojanowska, Maria .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2013, 49 (06) :1093-1101
[22]   Origin and function of myofibroblasts in kidney fibrosis [J].
LeBleu, Valerie S. ;
Taduri, Gangadhar ;
O'Connell, Joyce ;
Teng, Yingqi ;
Cooke, Vesselina G. ;
Woda, Craig ;
Sugimoto, Hikaru ;
Kalluri, Raghu .
NATURE MEDICINE, 2013, 19 (08) :1047-1054
[23]   Snail1, Snail2, and E47 promote mammary epithelial branching morphogenesis [J].
Lee, KangAe ;
Gjorevski, Nikolce ;
Boghaert, Eline ;
Radisky, Derek C. ;
Nelson, Celeste M. .
EMBO JOURNAL, 2011, 30 (13) :2662-2674
[24]   Inhibition of angiogenesis by a mouse sprouty protein [J].
Lee, SH ;
Schloss, DJ ;
Jarvis, L ;
Krasnow, MA ;
Swain, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (06) :4128-4133
[25]   Slug is required for cell survival during partial epithelial-mesenchymal transition of HGF-induced tubulogenesis [J].
Leroy, Pascale ;
Mostov, Keith E. .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (05) :1943-1952
[26]   Protein Kinase Cδ and c-Abl Kinase Are Required for Transforming Growth Factor β Induction of Endothelial-Mesenchymal Transition In Vitro [J].
Li, Zhaodong ;
Jimenez, Sergio A. .
ARTHRITIS AND RHEUMATISM, 2011, 63 (08) :2473-2483
[27]   Gene alterations identified by expression profiling in tumor-associated endothelial cells from invasive ovarian carcinoma [J].
Lu, Chunhula ;
Bonome, Tomas ;
Li, Yang ;
Kamat, Aparna A. ;
Han, Liz Y. ;
Schmandt, Rosemarie ;
Coleman, Robert L. ;
Gershenson, David M. ;
Jaffe, Robert B. ;
Birrer, Michael J. ;
Sood, Anil K. .
CANCER RESEARCH, 2007, 67 (04) :1757-1768
[28]   Transforming growth factor-β2 promotes Snail-mediated endothelial-mesenchymal transition through convergence of Smad-dependent and Smad-independent signalling [J].
Medici, Damian ;
Potenta, Scott ;
Kalluri, Raghu .
BIOCHEMICAL JOURNAL, 2011, 437 :515-520
[29]   Resident fibroblast lineages mediate pressure overload-induced cardiac fibrosis [J].
Moore-Morris, Thomas ;
Guimaraes-Camboa, Nuno ;
Banerjee, Indroneal ;
Zambon, Alexander C. ;
Kisseleva, Tatiana ;
Velayoudon, Aurelie ;
Stallcup, William B. ;
Gu, Yusu ;
Dalton, Nancy D. ;
Cedenilla, Marta ;
Gomez-Amaro, Rafael ;
Zhou, Bin ;
Brenner, David A. ;
Peterson, Kirk L. ;
Chen, Ju ;
Evans, Sylvia M. .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (07) :2921-2934
[30]  
Nakajima Y, 2000, ANAT RECORD, V258, P119, DOI 10.1002/(SICI)1097-0185(20000201)258:2<119::AID-AR1>3.0.CO