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A role for the growth factor Bone Morphogenetic Protein 7 in early development of the murine eye.

机译:生长因子骨形态发生蛋白7在鼠眼早期发育中的作用。

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摘要

The early steps of mouse eye development involve a series of inductive interactions between the optic vesicle and adjacent head ectoderm. Signals from the optic vesicle induce a thickening of the head ectoderm known as the lens placode, which ultimately invaginates to form the adult lens. However, while necessary for lens induction, the optic vesicle is not sufficient, as additional signals are required to establish the ectoderm's ability to respond to lens-inducing stimuli. Thus, rather than resulting from a single signaling event, lens induction is coordinated by a sequence of signals combining to govern eye formation. The experiments described here identify a role for Bmp7, a member of the Bone Morphogenetic Protein (BMP) family of growth factors, as one of these regulators of mouse lens placode induction. Previous studies show that targeted inactivation of Bmp7 leads to eye defects with late onset and variable expressivity. However, I demonstrate a marked increase in the severity of the Bmp7 mutant phenotype in a C3H/He genetic background. This increased expressivity has allowed analysis of Bmp7's role in early lens development.;To integrate Bmp7 into a genetic pathway controlling lens placode formation, the expression of early lens placode-specific markers was examined in embryos mutant either for Bmp7 or for the transcription factor Pax6, which is critical for lens placode induction. These experiments suggest a model in which Bmp7 is not required for lens placode induction, but is necessary immediately thereafter, during a pre-placodal stage of lens development. Since Bmp7 and its receptors are widely expressed in the eye-forming region, it is unclear whether the observed lens placode defects reflect Bmp7 function in the head ectoderm, the optic vesicle, or both. To address this question, a tissue recombination system was used to show that Bmp7−/− optic vesicle cannot induce lenses in wild-type ectoderm, nor can wild-type optic vesicle instruct lens induction in Bmp7−/− ectoderm. Thus, Bmp7 is required tissue autonomously in both the lens ectoderm and the optic vesicle, suggesting multiple roles for Bmp7 in early oculogenesis.
机译:小鼠眼睛发育的早期步骤涉及囊泡与邻近的头部外胚层之间的一系列感应相互作用。来自视神经小泡的信号会引起称为晶状体基底膜的头部外胚层增厚,并最终形成成人晶状体。然而,尽管对于晶状体诱导是必要的,但视神经泡是不够的,因为需要额外的信号来建立外胚层对晶状体诱导的刺激作出反应的能力。因此,不是由单个信号事件引起,而是由一系列信号组合来协调晶状体感应,以控制眼睛的形成。此处描述的实验确定了Bmp7(一种小鼠​​骨形态发生蛋白(BMP)生长因子家族的成员)的作用,它是小鼠晶状体诱导的这些调节剂之一。先前的研究表明,Bmp7的靶向失活会导致眼部疾病,且起病较晚,且表现力可变。但是,我证明了在C3H / He遗传背景下Bmp7突变表型的严重性显着增加。这种增加的表达能力可以分析Bmp7在早期晶状体发育中的作用。;为了将Bmp7整合到控制晶状体斑形成的遗传途径中,在Bmp7或转录因子Pax6的胚胎突变体中检查了早期晶状斑特定标记的表达。 ,这对于晶状体基板诱导至关重要。这些实验提出了一种模型,其中在晶状体发育的前斑灭阶段中,不需要Bmp7进行晶状体斑块诱导,但是此后立即需要Bmp7。由于Bmp7及其受体在眼睛形成区域广泛表达,因此尚不清楚观察到的晶状体斑缺陷是否反映了Bmp7在头部外胚层,视神经泡囊或两者中的功能。为了解决这个问题,组织重组系统用于显示Bmp7-/-囊泡不能在野生型外胚层中诱导晶状体,野生型囊泡也不能在Bmp7-/-外胚层中指示晶状体诱导。因此,Bmp7是晶状体外胚层和视神经囊泡中自主需要的组织,表明Bmp7在早期眼球发生中具有多种作用。

著录项

  • 作者

    Wawersik, Stefan Charles.;

  • 作者单位

    Harvard University.;

  • 授予单位 Harvard University.;
  • 学科 Biology Genetics.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 169 p.
  • 总页数 169
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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