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海鞘胚胎中神经索和脊索细胞命运的二元规范。

Binary specification of nerve cord and notochord cell fates in ascidian embryos.

作者信息

Minokawa T, Yagi K, Makabe K W, Nishida H

机构信息

Department of Biological Sciences, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.

出版信息

Development. 2001 Jun;128(11):2007-17. doi: 10.1242/dev.128.11.2007.

Abstract

In the ascidian embryo, the nerve cord and notochord of the tail of tadpole larvae originate from the precursor blastomeres for both tissues in the 32-cell-stage embryo. Each fate is separated into two daughter blastomeres at the next cleavage. We have examined mechanisms that are responsible for nerve cord and notochord specification through experiments involving blastomere isolation, cell dissociation, and treatment with basic fibroblast growth factor (bFGF) and inhibitors for the mitogen-activated protein kinase (MAPK) cascade. It has been shown that inductive cell interaction at the 32-cell stage is required for notochord formation. Our results show that the nerve cord fate is determined autonomously without any cell interaction. Presumptive notochord blastomeres also assume a nerve cord fate when they are isolated before induction is completed. By contrast, not only presumptive notochord blastomeres but also presumptive nerve cord blastomeres forsake their default nerve cord fate and choose the notochord fate when they are treated with bFGF. When the FGF-Ras-MAPK signaling cascade is inhibited, both blastomeres choose the default nerve cord pathway, supporting the results of blastomere isolation. Thus, binary choice of alternative fates and asymmetric division are involved in this nerve cord/notochord fate determination system, mediated by FGF signaling.

摘要

在海鞘胚胎中,蝌蚪幼虫尾部的神经索和脊索起源于32细胞期胚胎中这两种组织的前体卵裂球。在接下来的一次卵裂时,每种命运被分隔到两个子卵裂球中。我们通过涉及卵裂球分离、细胞解离以及用碱性成纤维细胞生长因子(bFGF)和有丝分裂原激活蛋白激酶(MAPK)级联抑制剂处理的实验,研究了负责神经索和脊索特化的机制。已表明,32细胞期的诱导性细胞相互作用是脊索形成所必需的。我们的结果表明,神经索命运是自主决定的,无需任何细胞相互作用。在诱导完成前分离时,推定的脊索卵裂球也会呈现神经索命运。相比之下,当用bFGF处理时,不仅推定的脊索卵裂球,而且推定的神经索卵裂球都会放弃其默认的神经索命运而选择脊索命运。当FGF-Ras-MAPK信号级联被抑制时,两个卵裂球都选择默认的神经索途径,这支持了卵裂球分离的结果。因此,由FGF信号介导的这种神经索/脊索命运决定系统涉及两种命运的二元选择和不对称分裂。

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