Liguori Giovanna L, Echevarria Diego, Bonilla Sonia, D'Andrea Daniela, Liguoro Annamaria, Persico Maria G, Martinez Salvador
Institute of Genetics and Biophysics A. Buzzati-Traverso, CNR, Via Pietro Castellino 111, Naples 80131, Italy.
Int J Dev Biol. 2009;53(4):549-57. doi: 10.1387/ijdb.082650gl.
During development of the mammalian embryo, there is a complex relation between formation of the mesoderm and the neuroectoderm. In mouse, for example, the role of the node and its mesendoderm derivatives in anterior neural specification is still debated. Mouse Cripto(-/-) embryos could potentially help settle this debate because they lack almost all embryonic endoderm and mesoderm, including the node and its derivatives. In the present paper, we show that Cripto(-/-) embryos can still form functional neural stem cells that are able to differentiate and maintain a neural phenotype both in vivo and in vitro. These data suggest that signals emanating from the mesoderm and endoderm might not be essential for the formation and differentiation of neural stem cells. However, we use grafting experiments to show that the Cripto(-/-) isthmus (the secondary organizer located at the midbrain-hindbrain boundary) loses its inductive ability. We further show that the Cripto(-/-)isthmus expresses lower amounts of the isthmic signalling molecule, Fgf8. Since nearby tissues remain competent to respond to exogenously added Fgf8, this reduction in Fgf8 levels in the Cripto(-/-) isthmus is the potential cause of the loss of patterning ability in graft experiments. Overall, we interpret our data to suggest that the mammalian node and primitive streak are essential for the development of the regional identities that control the specification and formation of the secondary organizers within the developing brain.
在哺乳动物胚胎发育过程中,中胚层和神经外胚层的形成之间存在复杂的关系。例如,在小鼠中,节点及其中内胚层衍生物在头部神经特化中的作用仍存在争议。小鼠Cripto(-/-)胚胎可能有助于解决这一争议,因为它们几乎缺乏所有胚胎内胚层和中胚层,包括节点及其衍生物。在本文中,我们表明Cripto(-/-)胚胎仍能形成功能性神经干细胞,这些细胞在体内和体外都能分化并维持神经表型。这些数据表明,来自中胚层和内胚层的信号可能对神经干细胞的形成和分化不是必需的。然而,我们通过移植实验表明,Cripto(-/-)峡部(位于中脑-后脑边界的次级组织者)失去了其诱导能力。我们进一步表明,Cripto(-/-)峡部表达的峡部信号分子Fgf8的量较低。由于附近组织对外源添加的Fgf8仍有反应能力,Cripto(-/-)峡部中Fgf8水平的降低是移植实验中模式形成能力丧失的潜在原因。总体而言,我们对数据的解释表明,哺乳动物的节点和原条对于控制发育中大脑内次级组织者的特化和形成的区域身份的发育至关重要。