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
[21]   Frzb modulates Wnt-9a-mediated β-catenin signaling during avian atrioventricular cardiac cushion development [J].
Person, AD ;
Garriock, RJ ;
Krieg, PA ;
Runyan, RB ;
Klewer, SE .
DEVELOPMENTAL BIOLOGY, 2005, 278 (01) :35-48
[22]   EPITHELIAL MESENCHYMAL CELL-TRANSFORMATION IN THE EMBRYONIC HEART CAN BE MEDIATED, IN PART, BY TRANSFORMING GROWTH FACTOR-BETA [J].
POTTS, JD ;
RUNYAN, RB .
DEVELOPMENTAL BIOLOGY, 1989, 134 (02) :392-401
[23]   SENSE AND ANTISENSE TGF-BETA-3 MESSENGER-RNA LEVELS CORRELATE WITH CARDIAC-VALVE INDUCTION [J].
POTTS, JD ;
VINCENT, EB ;
RUNYAN, RB ;
WEEKS, DL .
DEVELOPMENTAL DYNAMICS, 1992, 193 (04) :340-345
[24]   EPITHELIAL MESENCHYMAL TRANSFORMATION OF EMBRYONIC CARDIAC ENDOTHELIAL-CELLS IS INHIBITED BY A MODIFIED ANTISENSE OLIGODEOXYNUCLEOTIDE TO TRANSFORMING GROWTH-FACTOR BETA-3 [J].
POTTS, JD ;
DAGLE, JM ;
WALDER, JA ;
WEEKS, DL ;
RUNYAN, RB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) :1516-1520
[25]   Slug is a mediator of epithelial-mesenchymal cell transformation in the developing chicken heart [J].
Romano, LA ;
Runyan, RB .
DEVELOPMENTAL BIOLOGY, 1999, 212 (01) :243-254
[26]   Utilization of antisense oligodeoxynucleotides with embryonic tissues in culture [J].
Runyan, RB ;
Wendler, CC ;
Romano, LA ;
Boyer, AS ;
Dagle, JM ;
Weeks, DL .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1999, 18 (03) :316-324
[27]   SIGNAL TRANSDUCTION OF A TISSUE INTERACTION DURING EMBRYONIC HEART DEVELOPMENT [J].
RUNYAN, RB ;
POTTS, JD ;
SHARMA, RV ;
LOEBER, CP ;
CHIANG, JJ ;
BHALLA, RC .
CELL REGULATION, 1990, 1 (03) :301-313
[28]   INVASION OF MESENCHYME INTO 3-DIMENSIONAL COLLAGEN GELS - A REGIONAL AND TEMPORAL ANALYSIS OF INTERACTION IN EMBRYONIC HEART-TISSUE [J].
RUNYAN, RB ;
MARKWALD, RR .
DEVELOPMENTAL BIOLOGY, 1983, 95 (01) :108-114
[29]   TGF-BETA-3-MEDIATED TISSUE INTERACTION DURING EMBRYONIC HEART DEVELOPMENT [J].
RUNYAN, RB ;
POTTS, JD ;
WEEKS, DL .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1992, 32 (02) :152-159
[30]   siRNA and miRNA: an insight into RISCs [J].
Tang, GL .
TRENDS IN BIOCHEMICAL SCIENCES, 2005, 30 (02) :106-114