Hara K, Kimura J, Ide H
Biological Institute, Tohoku University, Sendai, Japan.
Int J Dev Biol. 1998 May;42(4):591-9.
The apical mesodermal region of chick limb buds (progress zone, PZ) which is essential for limb pattern formation contains uncommitted cells that change their positional values instructed by the apical ectodermal ridge (AER). Reciprically, the PZ cells maintain the AER activity. FGF-2 and FGF-4 can substitute for the AER to maintain normal outgrowth and gene expression in the limb bud. We examined the effects of FGF on the maintenance of PZ cells characteristics in culture by making recombinant limbs with anterior PZ cells that were pre-cultured in the presence of FGF-2 or FGF-4 and analyzed their morphogenic potency and responsiveness to positional cues arising from the zone of polarizing activity (ZPA). The limb buds expressed distal Hox genes and could form a segmented digit. Recombinant limb buds consisting of anterior PZ cells cultured without FGF failed to express Hox genes and formed instead a small cartilage nodule. These results indicate that addition of FGF-2 or FGF-4 to cultured PZ cells maintains their competence for Hox gene expression and digit formation, but not their responsiveness to positional cues from the ZPA. We also found that when anterior PZ cells which had been pre-cultured with FGF-2 or FGF-4 were implanted underneath the AER, they could maintain Fgf-8 expression in the AER, whereas this expression was not detected in the AER on the grafted anterior PZ cells that had been pre-cultured without FGF, indicating that FGF maintains AER-maintenance activity of PZ cells in culture.
鸡胚肢体芽顶端中胚层区域(进展区,PZ)对于肢体模式形成至关重要,其中包含未分化的细胞,这些细胞会根据顶端外胚层嵴(AER)的指示改变其位置值。相反,PZ细胞维持AER的活性。FGF-2和FGF-4可以替代AER来维持肢体芽的正常生长和基因表达。我们通过用在FGF-2或FGF-4存在下预培养的前PZ细胞构建重组肢体,研究了FGF对培养中PZ细胞特性维持的影响,并分析了它们的形态发生潜能以及对来自极化活性区(ZPA)的位置信号的反应性。肢体芽表达远端Hox基因并能形成分节的指。由未添加FGF培养的前PZ细胞组成的重组肢体芽未能表达Hox基因,而是形成了一个小软骨结节。这些结果表明,向培养的PZ细胞中添加FGF-2或FGF-4可维持它们对Hox基因表达和指形成的能力,但不能维持它们对来自ZPA的位置信号的反应性。我们还发现,当用FGF-2或FGF-4预培养的前PZ细胞植入AER下方时,它们可以维持AER中Fgf-8的表达,而在未用FGF预培养的移植前PZ细胞的AER中未检测到这种表达,这表明FGF在培养中维持PZ细胞的AER维持活性。