Latrophilin-2 is a novel component of the epithelial-mesenchymal transition within the atrioventricular canal of the embryonic chicken heart

被引:34
作者
Doyle, Sally E.
Scholz, Matthew J.
Greer, Kevin A.
Hubbard, Antony D.
Darnell, Diana K.
Antin, Parker B.
Klewer, Scott E.
Runyan, Raymond B.
机构
[1] Univ Arizona, Dept Cell Biol & Anat, Tucson, AZ 85724 USA
[2] Univ Arizona, Dept Biomed Engn, Tucson, AZ 85721 USA
[3] Univ Arizona, Dept Pediat Cardiol, Tucson, AZ 85721 USA
关键词
EMT; cardiac development; microarray; valvulosepatal development; cardiac cushions; TGF-beta; pertussis toxin;
D O I
10.1002/dvdy.20973
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Endothelial cells in the atrioventricular canal of the heart undergo an epithelial-mesenchymal transition (EMT) to form heart valves. We surveyed an on-line database (http://www.geisha.arizona.edu/) for clones expressed during gastrulation to identify novel EMT components. One gene, latrophilin-2, was identified as expressed in the heart and appeared to be functional in EMT. This molecule was chosen for further examination. In situ localization showed it to be expressed in both the myocardium and endothelium. Several antisense DNA probes and an siRNA for latrophilin-2 produced a loss of EMT in collagen gel cultures. Latrophilin-2 is a putative G-protein-coupled receptor and we previously identified a pertussis toxin-sensitive G-protein signal transduction pathway. Microarray experiments were performed to examine whether these molecules were related. After treatment with antisense DNA against latrophilin-2, expression of 1,385 genes and ESTs was altered. This represented approximately 12.5% of the microarray elements. In contrast, pertussis toxin altered only 103 (0.9%) elements of the array. There appears to be little overlap between the two signal transduction pathways. Latrophilin-2 is thus a novel component of EMT and provides a new avenue for investigation of this cellular process.
引用
收藏
页码:3213 / 3221
页数:9
相关论文
共 34 条
[1]   Transforming growth factor beta in cardiovascular development and function [J].
Azhar, M ;
Schultz, JEJ ;
Grupp, I ;
Dorn, GW ;
Meneton, P ;
Molin, DGM ;
Gittenberger-de Groot, AC ;
Doetschman, T .
CYTOKINE & GROWTH FACTOR REVIEWS, 2003, 14 (05) :391-407
[2]  
Bakin AV, 2002, J CELL SCI, V115, P3193
[3]   GEISHA, a whole-mount in situ hybridization gene expression screen in chicken embryos [J].
Bell, GW ;
Yatskievych, TA ;
Antin, PB .
DEVELOPMENTAL DYNAMICS, 2004, 229 (03) :677-687
[4]   TGFβ2 and TGFβ3 have separate and sequential activities during epithelial-mesenchymal cell transformation in the embryonic heart [J].
Boyer, AS ;
Ayerinskas, II ;
Vincent, EB ;
McKinney, LA ;
Weeks, DL ;
Runyan, RB .
DEVELOPMENTAL BIOLOGY, 1999, 208 (02) :530-545
[5]  
Boyer AS, 1999, DEV DYNAM, V214, P81
[6]   Requirement of type III TGF-β receptor for endocardial cell transformation in the heart [J].
Brown, CB ;
Boyer, AS ;
Runyan, RB ;
Barnett, JV .
SCIENCE, 1999, 283 (5410) :2080-2082
[7]   Antibodies to the type II TGF beta receptor block cell activation and migration during atrioventricular cushion transformation in the heart [J].
Brown, CB ;
Boyer, AS ;
Runyan, RB ;
Barnett, JV .
DEVELOPMENTAL BIOLOGY, 1996, 174 (02) :248-257
[8]   Temporal and distinct TGFβ ligand requirements during mouse and avian endocardial cushion morphogenesis [J].
Camenisch, TD ;
Molin, DGM ;
Person, A ;
Runyan, RB ;
Gittenberger-de Groot, AC ;
McDonald, JA ;
Klewer, SE .
DEVELOPMENTAL BIOLOGY, 2002, 248 (01) :170-181
[9]   Calcium oscillations increase the efficiency and specificity of gene expression [J].
Dolmetsch, RE ;
Xu, KL ;
Lewis, RS .
NATURE, 1998, 392 (6679) :933-936
[10]   Reliability and reproducibility issues in DNA microarray measurements [J].
Draghici, S ;
Khatri, P ;
Eklund, AC ;
Szallasi, Z .
TRENDS IN GENETICS, 2006, 22 (02) :101-109