FGF-8 in the ventral pharynx alters development of myocardial calcium transients after neural crest ablation

被引:44
作者
Farrell, MJ
Burch, JL
Wallis, K
Rowley, L
Kumiski, D
Stadt, H
Godt, RE
Creazzo, TL
Kirby, ML
机构
[1] Duke Univ, Med Ctr, Dept Pediat, Div Neonatol, Durham, NC 27710 USA
[2] Med Coll Georgia, Dept Physiol, Augusta, GA 30912 USA
[3] Med Coll Georgia, Dept Cellular Biol & Anat, Augusta, GA 30912 USA
关键词
D O I
10.1172/JCI9317
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cardiac neural crest ablation results in depressed myocardial calcium transients and elevated proliferation in myocardium at a stage when cardiac neural crest cells are not in contact with the myocardium. To test the hypothesis that cardiac neural crest-derived cells, which migrate into the caudal, ventral pharynx at stage 14, block a signal from the ventral pharynx, we cultured stage 12 chick heart tube or myocardial strips in the presence or absence of ventral pharynx. We found that myocardium cultured with ventral pharynx that had not yet contacted neural crest cells had significantly reduced calcium transients and an increased rate of proliferation. Ventral. pharynx from intact embryos at a stage when neural crest-derived cells had reached the pharynx had no effect on myocardial calcium transients. Ventral pharynx from neural crest-ablated embryos continued to suppress myocardial calcium transients at this later stage. Myocardium cultured with FGF-2 also showed a significant reduction in calcium transients. An FGF-2- neutralizing Ab reversed the deleterious effect of the ventral pharynx on myocardial calcium transients and proliferation. We therefore examined the expression of FGF-2 and similar FGFs in the ventral pharynx. Only FGF-8 was expressed in a temporospatial pattern that made it a viable candidate for altering the myocardial calcium transient during stages 14-18. In explant cultures, neutralizing Ab for FGF-8 rescued development of the myocardial calcium transient in neural crest-ablated chick embryos.
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收藏
页码:1509 / 1517
页数:9
相关论文
共 36 条
  • [11] HEMODYNAMICS OF THE STAGE-12 TO STAGE-29 CHICK-EMBRYO
    HU, N
    CLARK, EB
    [J]. CIRCULATION RESEARCH, 1989, 65 (06) : 1665 - 1670
  • [12] Negative inotropic effect of basic fibroblast growth factor on adult rat cardiac myocyte
    Ishibashi, Y
    Urabe, Y
    Tsutsui, H
    Kinugawa, S
    Sugimachi, M
    Takahashi, M
    Yamamoto, S
    Tagawa, P
    Sunagawa, K
    Takeshita, A
    [J]. CIRCULATION, 1997, 96 (08) : 2501 - 2504
  • [13] HEART INDUCTION IN SALAMANDERS
    JACOBSON, AG
    DUNCAN, JT
    [J]. JOURNAL OF EXPERIMENTAL ZOOLOGY, 1968, 167 (01): : 79 - &
  • [14] BACKTRANSPLANTATION OF CHICK CARDIAC NEURAL CREST CELLS CULTURED IN LIF RESCUES HEART DEVELOPMENT
    KIRBY, ML
    KUMISKI, DH
    MYERS, T
    CERJAN, C
    MISHIMA, N
    [J]. DEVELOPMENTAL DYNAMICS, 1993, 198 (04) : 296 - 311
  • [15] NEURAL CREST CELLS CONTRIBUTE TO NORMAL AORTICOPULMONARY SEPTATION
    KIRBY, ML
    GALE, TF
    STEWART, DE
    [J]. SCIENCE, 1983, 220 (4601) : 1059 - 1061
  • [16] MIGRATION AND DISTRIBUTION OF CIRCUMPHARYNGEAL CREST CELLS IN THE CHICK-EMBRYO - FORMATION OF THE CIRCUMPHARYNGEAL RIDGE AND E/C8+ CREST CELLS IN THE VERTEBRATE HEAD REGION
    KURATANI, SC
    KIRBY, ML
    [J]. ANATOMICAL RECORD, 1992, 234 (02): : 263 - 280
  • [17] HEMODYNAMIC-CHANGES - WALL STRESSES AND PRESSURE-GRADIENTS IN NEURAL CREST-ABLATED CHICK-EMBRYOS
    LEATHERBURY, L
    BRADEN, DS
    TOMITA, H
    GAULDIN, HE
    JACKSON, WF
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1990, 588 : 305 - 313
  • [18] HEMODYNAMIC-CHANGES AND COMPENSATORY MECHANISMS DURING EARLY CARDIOGENESIS AFTER NEURAL CREST ABLATION IN CHICK-EMBRYOS
    LEATHERBURY, L
    CONNUCK, DM
    GAULDIN, HE
    KIRBY, ML
    [J]. PEDIATRIC RESEARCH, 1991, 30 (06) : 509 - 512
  • [19] LEDOUARIN N, 1992, NEURAL CREST
  • [20] Hemodynamic abnormalities in fetuses with congenital heart disease
    Lutin, WA
    Brumund, MR
    Jones, C
    Tharpe, CE
    Montegomery, M
    McCaffrey, FM
    [J]. PEDIATRIC CARDIOLOGY, 1999, 20 (06) : 390 - 395