Tam P P, Trainor P A
Embryology Unit, Children's Medical Research Institute, Wentworthville, NSW, Australia.
Anat Embryol (Berl). 1994 Apr;189(4):275-305. doi: 10.1007/BF00190586.
Somite formation in the mouse embryo begins with the recruitment of mesenchymal cells into the paraxial mesoderm. Cells destined for the paraxial mesoderm are recruited from a progenitor population found first in the embryonic ectoderm and later in the primitive streak and the tail bud. Experimental evidence suggests that the allocation of precursor cells to different mesodermal lineages may be related to the site at which the cells ingress through the primitive streak. An increasing number of genes, such as those encoding growth factor and transcription factors, are now known to be expressed in the primitive streak. It is not known whether the specification of mesodermal cell fate has any relationship with the activity of genes that are expressed in the restricted cell populations of the primitive streak. Somitomeres, which are spherical clusters of mesenchymal cells in the presomitic mesoderm, presage the segmentation of somites in the paraxial mesoderm. The somitomeric organization denotes a pre-pattern of segmentation that defines the physical boundary and the bilateral symmetry of the mesodermal segments in the body axis. The establishment of new somitomeres seems to require the interaction of a resident cell population in the presomitic mesoderm and the incoming primitive streak cells. Cell mixing, which occurs in the somitomeres prior to somite segmentation, poses problems in understanding the developmental role of the somitomere and the real significance of the partitioning of the node-derived and primitive streak-derived cells in the mesodermal segments. In the presomitic mesoderm, the expression of some genes that encode transcription factors, growth factors or tyrosine kinase receptor, and the localization of certain cell adhesion molecules are closely associated with distinct morphogenetic events, such as cell clustering in the presomitic mesoderm and the formation of epithelial somites. There is, however, very little direct relationship between the spatial pattern of gene expression and the somitomeric organization in the presomitic mesoderm. Results of somite transplantation experiments suggest that both the segmental address and the morphogenetic characteristics of the somite may be determined during somite segmentation. Regional identity of the paraxial mesodermal segment is conferred by the expression of a combination of Hox genes in the sclerotome and probably other lineage-specific genes that are subject to imprinting. Superimposed on the global metameric pattern, two orthogonal polarities of cell differentiation are endowed in each mesodermal segment. The rostro-caudal polarity is established prior to somite segmentation. This polarity is later manifested by the subdivision of the sclerotome and the alliance of the neural crest cells and motor axons with the rostral half-somite.(ABSTRACT TRUNCATED AT 400 WORDS)
小鼠胚胎中体节的形成始于间充质细胞被招募进入轴旁中胚层。注定要进入轴旁中胚层的细胞是从最初在胚胎外胚层、随后在原条和尾芽中发现的祖细胞群体中招募而来的。实验证据表明,前体细胞向不同中胚层谱系的分配可能与细胞通过原条进入的位点有关。现在已知越来越多的基因,如那些编码生长因子和转录因子的基因,在原条中表达。尚不清楚中胚层细胞命运的特化是否与在原条受限细胞群体中表达的基因活性有任何关系。体节球是前体中胚层中间充质细胞的球形簇,预示着轴旁中胚层中体节的分割。体节球的组织表示一种预分割模式,它定义了身体轴上中胚层节段的物理边界和双侧对称性。新体节球的形成似乎需要前体中胚层中常驻细胞群体与进入的原条细胞之间的相互作用。在体节分割之前在体节球中发生的细胞混合,给理解体节球的发育作用以及中胚层节段中节点来源和原条来源细胞的划分的真正意义带来了问题。在前体中胚层中,一些编码转录因子、生长因子或酪氨酸激酶受体的基因的表达,以及某些细胞粘附分子的定位,与不同的形态发生事件密切相关,如前体中胚层中的细胞聚集和上皮体节的形成。然而,基因表达的空间模式与前体中胚层中的体节球组织之间几乎没有直接关系。体节移植实验的结果表明,体节的节段地址和形态发生特征可能在体节分割期间就已确定。轴旁中胚层节段的区域身份是由硬骨节中一组Hox基因以及可能其他受印记影响的谱系特异性基因的表达赋予的。叠加在整体节段模式上,每个中胚层节段都具有两种正交的细胞分化极性。头-尾极性在体节分割之前就已确立。这种极性随后表现为硬骨节的细分以及神经嵴细胞和运动轴突与头侧半体节的联合。(摘要截选至400字)