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斑马鱼心脏的诱导和分化需要成纤维细胞生长因子8(fgf8/小脑缺失)。

Induction and differentiation of the zebrafish heart requires fibroblast growth factor 8 (fgf8/acerebellar).

作者信息

Reifers F, Walsh E C, Léger S, Stainier D Y, Brand M

机构信息

Department of Neurobiology, University of Heidelberg, Im Neuenheimer Feld 364, D-69120 Heidelberg, Germany.

出版信息

Development. 2000 Jan;127(2):225-35. doi: 10.1242/dev.127.2.225.

Abstract

Vertebrate heart development is initiated from bilateral lateral plate mesoderm that expresses the Nkx2.5 and GATA4 transcription factors, but the extracellular signals specifying heart precursor gene expression are not known. We describe here that the secreted signaling factor Fgf8 is expressed in and required for development of the zebrafish heart precursors, particularly during initiation of cardiac gene expression. fgf8 is mutated in acerebellar (ace) mutants, and homozygous mutant embryos do not establish normal circulation, although vessel formation is only mildly affected. In contrast, heart development, in particular of the ventricle, is severely abnormal in acerebellar mutants. Several findings argue that Fgf8 has a direct function in development of cardiac precursor cells: fgf8 is expressed in cardiac precursors and later in the heart ventricle. Fgf8 is required for the earliest stages of nkx2.5 and gata4, but not gata6, expression in cardiac precursors. Cardiac gene expression is restored in acerebellar mutant embryos by injecting fgf8 RNA, or by implanting a Fgf8-coated bead into the heart primordium. Pharmacological inhibition of Fgf signalling during formation of the heart primordium phenocopies the acerebellar heart phenotype, confirming that Fgf signaling is required independently of earlier functions during gastrulation. These findings show that fgf8/acerebellar is required for induction and patterning of myocardial precursors.

摘要

脊椎动物心脏发育起始于表达Nkx2.5和GATA4转录因子的双侧侧板中胚层,但决定心脏前体基因表达的细胞外信号尚不清楚。我们在此描述,分泌的信号因子Fgf8在斑马鱼心脏前体的发育中表达且是必需的,特别是在心脏基因表达起始阶段。在小脑缺失(ace)突变体中,fgf8发生突变,纯合突变体胚胎虽血管形成仅受到轻微影响,但无法建立正常循环。相反,小脑缺失突变体的心脏发育,尤其是心室发育,严重异常。多项研究结果表明,Fgf8在心脏前体细胞的发育中具有直接作用:fgf8在心脏前体中表达,随后在心室中表达。Fgf8是心脏前体中nkx2.5和gata4而非gata6表达的最早阶段所必需的。通过注射fgf8 RNA或将包被有Fgf8的珠子植入心脏原基,可使小脑缺失突变体胚胎中的心脏基因表达恢复。在心脏原基形成过程中对Fgf信号进行药理学抑制可模拟小脑缺失的心脏表型,证实Fgf信号在原肠胚形成过程中独立于早期功能是必需的。这些发现表明,fgf8/小脑缺失对于心肌前体的诱导和模式形成是必需的。

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