Wassef M, Joyner A L
CNRS URA 1414, Ecole Normale Superieure, Paris, France.
Perspect Dev Neurobiol. 1997;5(1):3-16.
Experimental studies in chick and analysis of mouse mutants have provided a framework for studying the early developmental processes involved in specifying the cerebellar anlage. Fate mapping studies in chick have shown that at early stages the cerebellum derives from cells in the mesencephalon and metencephalon (mes-met). Transplantation studies in chick have implicated the mes-met junction (isthmus) as a source of secreted factors that organize development of the entire mes-met, perhaps by stimulating proliferation and specifying positional values across the region. Fgf-8 has been implicated as a major factor involved in the isthmus organizing activity. Gene expression studies indicate that the anterior and posterior expression domains of the homeobox genes Otx-2 and Gbx-2, respectively, are the earliest indication of a division of the brain. Furthermore, the Otx-2/Gbx-2 expression border later resides at the mes-met junction. Genetic studies in mouse have shown that Otx-2 and Gbx-2 are required for normal development of cells on both sides of the border. In addition, mutations affecting the secreted factor Wnt-1, which is expressed anterior to the Otx-2/Gbx-2 expression border and the homeodomain transcription factors, Engrailed-1,2 and Pax-2,5 that have broad overlapping expression domains in the mes-met, result in deletions of mes-met structures. Taken together, these studies suggest that specification of the cerebellar territory requires a hierarchy of complex cellular and genetic interactions that gradually subdivide the brain into smaller regions.
对鸡的实验研究以及对小鼠突变体的分析,为研究确定小脑原基所涉及的早期发育过程提供了一个框架。鸡的命运图谱研究表明,在早期阶段,小脑起源于中脑和后脑(中后脑)的细胞。鸡的移植研究表明,中后脑交界处(峡部)是分泌因子的来源,这些因子可能通过刺激增殖和确定该区域的位置值来组织整个中后脑的发育。Fgf-8被认为是参与峡部组织活动的主要因子。基因表达研究表明,同源框基因Otx-2和Gbx-2的前后表达域分别是大脑划分的最早迹象。此外,Otx-2/Gbx-2表达边界后来位于中后脑交界处。小鼠的遗传学研究表明,边界两侧的细胞正常发育需要Otx-2和Gbx-2。此外,影响分泌因子Wnt-1(在Otx-2/Gbx-2表达边界前方表达)以及同源域转录因子Engrailed-1、2和Pax-2、5(在中后脑具有广泛重叠的表达域)的突变会导致中后脑结构缺失。综上所述,这些研究表明,小脑区域的确定需要一系列复杂的细胞和遗传相互作用,这些相互作用逐渐将大脑细分为更小的区域。