Christ B, Ordahl C P
Institute of Anatomy, University of Freiburg, Germany.
Anat Embryol (Berl). 1995 May;191(5):381-96. doi: 10.1007/BF00304424.
We report on the formation and early differentiation of the somites in the avian embryo. The somites are derived from the avian embryo. The somites are derived from the mesoderm which, in the body (excluding the head), is subdivided into four compartments: the axial, paraxial, intermediate and lateral plate mesoderm. Somites develop from the paraxial mesoderm and constitute the segmental pattern of the body. They are formed in pairs by epithelialization, first at the cranial end of the paraxial mesoderm, proceeding caudally, while new mesenchyme cells enter the paraxial mesoderm as a consequence of gastrulation. After their formation, which depends upon cell-cell and cell-matrix interactions, the somites impose segmental pattern upon peripheral nerves and vascular primordia. The newly formed somite consists of an epithelial ball of columnar cells enveloping mesenchymal cells within a central cavity, the somitocoel. Each somite is surrounded by extracellular matrix material connecting the somite with adjacent structures. The competence to form skeletal muscle is a unique property of the somites and becomes realized during compartmentalization, under control of signals emanating from surrounding tissues. Compartmentalization is accompanied by altered patterns of expression of Pax genes within the somite. These are believed to be involved in the specification of somite cell lineages. Somites are also regionally specified, giving rise to particular skeletal structures at different axial levels. This axial specification appears to be reflected in Hox gene expression. MyoD is first expressed in the dorsomedial quadrant of the still epithelial somite whose cells are not yet definitely committed. During early maturation, the ventral wall of the somite undergoes an epithelio-mesenchymal transition forming the sclerotome. The sclerotome later becomes subdivided into rostral and caudal halves which are separated laterally by von Ebner's fissure. The lateral part of the caudal half of the sclerotome mainly forms the ribs, neural arches and pedicles of vertebrae, whereas within the lateral part of the rostral half the spinal nerve develops. The medially migrating sclerotomal cells form the peri-notochordal sheath, and later give rise to the vertebral bodies and intervertebral discs. The somitocoel cells also contribute to the sclerotome. The dorsal half of the somite remains epithelial and is referred to as the dermomyotome because it gives rise to the dermis of the back and the skeletal musculature. the cells located within the lateral half of the dermomyotome are the precursors of the muscles of the hypaxial domain of the body, whereas those in the medial half are precursors of the epaxial (back) muscles.(ABSTRACT TRUNCATED AT 400 WORDS)
我们报道了鸡胚中体节的形成及早期分化。体节源自鸡胚。体节由中胚层分化而来,在躯体(不包括头部)中,中胚层可分为四个部分:轴旁中胚层、近轴中胚层、中间中胚层和侧板中胚层。体节由近轴中胚层发育而来,构成躯体的节段模式。它们通过上皮化成对形成,首先在近轴中胚层的头端开始,向尾端推进,同时由于原肠胚形成,新的间充质细胞进入近轴中胚层。在其形成后,这依赖于细胞间和细胞与基质的相互作用,体节将节段模式赋予外周神经和血管原基。新形成的体节由柱状上皮细胞组成的球状物包裹着中央腔内的间充质细胞,即体节腔。每个体节被细胞外基质物质包围,该物质将体节与相邻结构相连。形成骨骼肌的能力是体节的独特特性,并在分隔过程中,在周围组织发出的信号控制下得以实现。分隔伴随着体节内Pax基因表达模式的改变。这些基因被认为参与体节细胞谱系的特化。体节在区域上也有特化,在不同的轴向水平产生特定的骨骼结构。这种轴向特化似乎反映在Hox基因的表达中。MyoD首先在仍为上皮性的体节的背内侧象限表达,其细胞尚未明确分化。在早期成熟过程中,体节的腹侧壁经历上皮 - 间充质转化,形成生骨节。生骨节随后分为头侧和尾侧两半,它们在外侧由埃布纳氏裂分开。生骨节尾侧半的外侧部分主要形成肋骨、椎骨的神经弓和椎弓根,而在头侧半的外侧部分内发育出脊神经。向内侧迁移的生骨节细胞形成围脊索鞘,随后产生椎体和椎间盘。体节腔细胞也为生骨节做出贡献。体节的背侧半保持上皮性,被称为皮肌节,因为它产生背部的真皮和骨骼肌。位于皮肌节外侧半的细胞是躯体轴下区域肌肉的前体,而内侧半的细胞是轴上(背部)肌肉的前体。(摘要截选至400字)