Temporal and distinct TGFβ ligand requirements during mouse and avian endocardial cushion morphogenesis

被引:235
作者
Camenisch, TD [1 ]
Molin, DGM
Person, A
Runyan, RB
Gittenberger-de Groot, AC
McDonald, JA
Klewer, SE
机构
[1] Mayo Clin, Dept Biochem & Mol Biol, Scottsdale, AZ 85259 USA
[2] Leiden Univ, Med Ctr, Dept Anat & Embryol, NL-2300 RC Leiden, Netherlands
[3] Univ Utah, VAMC, Dept Med, Salt Lake City, UT 84112 USA
[4] Univ Arizona, Coll Med, Dept Pediat, Tucson, AZ 85724 USA
[5] Univ Arizona, Coll Med, Dept Anat & Cell Biol, Tucson, AZ 85724 USA
关键词
endocardial cushions; TGF beta; heart development; atrioventricular canal; epithelial transformation;
D O I
10.1006/dbio.2002.0731
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The formation of endocardial cushions in the atrioventricular (AV) canal of the rudimentary heart requires epithelial-to-mesenchymal cell transformation (EMT). This is a complex developmental process regulated by multiple extracellular signals and transduction pathways. A collagen gel assay, long used to examine endocardial cushion development in avian models, is now being employed to investigate genetically engineered mouse models with abnormal heart morphogenesis. In this study, we determine interspecies variations for avian and mouse cultured endocardial cushion explants. Considering these observed morphologic differences, we also define the temporal requirements for TGFbeta2 and TGFbeta3 during mouse endocardial cushion morphogenesis. TGFbeta2 and TGFbeta3 blocking antibodies inhibit endothelial cell activation and transformation, respectively, in avian explants. In contrast, neutralizing TGFbeta2 inhibits cell transformation in the mouse, while TGFbeta3 antibodies have no effect on activation or transformation events. This functional requirement for TGFbeta2 is concomitant with expression of TGFbeta2, but not TGFbeta3, within mouse endocardial cushions at a time coincident with transformation. Thus, both TGFbeta2 and TGFbeta3 appear necessary for the full morphogenetic program of EMT in the chick, but only TGFbeta2 is expressed and obligatory for mammalian endocardial cushion cell transformation. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:170 / 181
页数:12
相关论文
共 36 条
  • [1] Bartram U, 2001, CIRCULATION, V103, P2745
  • [2] BERNANKE DH, 1979, TEX REP BIOL MED, V39, P271
  • [3] TGFβ type III and TGFβ type II receptors have distinct activities during epithelial-mesenchymal cell transformation in the embryonic heart
    Boyer, AS
    Runyan, RB
    [J]. DEVELOPMENTAL DYNAMICS, 2001, 221 (04) : 454 - 459
  • [4] TGFβ2 and TGFβ3 have separate and sequential activities during epithelial-mesenchymal cell transformation in the embryonic heart
    Boyer, AS
    Ayerinskas, II
    Vincent, EB
    McKinney, LA
    Weeks, DL
    Runyan, RB
    [J]. DEVELOPMENTAL BIOLOGY, 1999, 208 (02) : 530 - 545
  • [5] Requirement of type III TGF-β receptor for endocardial cell transformation in the heart
    Brown, CB
    Boyer, AS
    Runyan, RB
    Barnett, JV
    [J]. SCIENCE, 1999, 283 (5410) : 2080 - 2082
  • [6] Antibodies to the type II TGF beta receptor block cell activation and migration during atrioventricular cushion transformation in the heart
    Brown, CB
    Boyer, AS
    Runyan, RB
    Barnett, JV
    [J]. DEVELOPMENTAL BIOLOGY, 1996, 174 (02) : 248 - 257
  • [7] Disruption of hyaluronan synthase-2 abrogates normal cardiac morphogenesis and hyaluronan-mediated transformation of epithelium to mesenchyme
    Camenisch, TD
    Spicer, AP
    Brehm-Gibson, T
    Biesterfeldt, J
    Augustine, ML
    Calabro, A
    Kubalak, S
    Klewer, SE
    McDonald, JA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (03) : 349 - 360
  • [8] DICKSON MC, 1993, DEVELOPMENT, V117, P625
  • [9] DICKSON MC, 1995, DEVELOPMENT, V121, P1845
  • [10] Dor Y, 2001, DEVELOPMENT, V128, P1531