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非洲爪蟾胚胎中胚层细胞的形态学差异,被确定为对不同阈值浓度激活素的早期反应。

Morphological differences in Xenopus embryonic mesodermal cells are specified as an early response to distinct threshold concentrations of activin.

作者信息

Symes K, Yordán C, Mercola M

机构信息

Department of Cell Biology, Harvard Medical School, Boston, MA 02115.

出版信息

Development. 1994 Aug;120(8):2339-46. doi: 10.1242/dev.120.8.2339.

Abstract

The involution of presumptive mesoderm that occurs during amphibian gastrulation is a complex process requiring the coordinated action of a diverse range of cells. We show that cells with distinct morphologies, resembling each of those normally found in the involuting tissue of the Xenopus embryo, are induced in dispersed animal pole cells by different doses of the potent mesoderm-inducing factor activin. Each cell type is induced within a restricted dose range of activin concentrations, the boundaries of which are well demarcated shortly after activin treatment. In contrast, Brachyury and goosecoid, two genes thought to pattern the presumptive mesoderm, and the gene encoding platelet-derived growth factor receptor alpha, which is expressed in the mesoderm of gastrula stage embryos, are induced by broad, overlapping ranges of high activin concentrations at such early times. Similarly, the response of the gene encoding platelet-derived growth factor A, which is expressed normally in ectoderm of gastrula stage embryos, diminishes gradually as the activin concentration increases. Dose windows for the expression of these four genes narrow and become distinct from one another in cell aggregates after several hours in culture, suggesting that activin prompts a dynamic program of gene expression in induced mesoderm.

摘要

两栖类原肠胚形成过程中预定中胚层的内卷是一个复杂的过程,需要多种细胞的协同作用。我们发现,不同剂量的强效中胚层诱导因子激活素可诱导分散的动物极细胞产生形态各异的细胞,这些细胞类似于非洲爪蟾胚胎内卷组织中正常存在的细胞。每种细胞类型在激活素浓度的特定剂量范围内被诱导产生,激活素处理后不久,这些剂量范围的界限就清晰可辨。相比之下,两个被认为参与预定中胚层模式形成的基因Brachyury和goosecoid,以及在原肠胚期胚胎中胚层表达的血小板衍生生长因子受体α基因,在早期是由宽泛且重叠的高激活素浓度范围诱导产生的。同样,正常情况下在原肠胚期胚胎外胚层表达的血小板衍生生长因子A基因的表达反应,会随着激活素浓度的增加而逐渐减弱。培养数小时后,这四个基因表达的剂量窗口变窄并在细胞聚集体中彼此区分开来,这表明激活素促使诱导中胚层中基因表达的动态程序。

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