Jasch L G
Am J Anat. 1980 Jun;158(2):171-91. doi: 10.1002/aja.1001580207.
Forelimbs of the newt Notophthalmus (Triturus) viridescens were amputated at the wrist, and at 14 to 25 days, the new limb regenerates were removed by a razor-blade cut. After incubation of the isolated regenerates in a medium containing only inorganic salts, the epithelium was removed easily from the underlying mesenchyme. The surfaces separated in the salt solution were examined using scanning and transmission electron microscopy to evaluate the completeness of the separation and the extent of tissue damage near the plane of separation. Rarely was an epithelial cell found clinging to the mesenchymal surface, supporting previous light microscopic observations. The most apparent morphological damage was sustained by the basal epithelial cell surfaces, which exhibited blebbing; the formation of vacant vesicles within the cytoplasm near the newly exposed plasma membranes; the structural disruption of some organelles; and the tearing away of fragments of the basal epithelial cell plasma membranes, which remained adherent to the mesenchymal surface during separation procedure. Examination of the structure of the epithelial-mesenchymal interface of intact regenerates showed that the plane of epithelial-mesenchymal separation was, for the most part, between the basal epithelial cell membrane and its substrate, an extracellular material which remained at the mesenchymal surface after separation. This substrate was in the form of an extracellular material closely adherent to the basal epithelial cell membrane at the distal tips of the regenerates; a developing basal lamina at the periphery of regenerates undergoing blastema accumulation; or a mature basal lamina at the base of digit stage regenerates. The usefulness of these separated tissues for future experimentation and the evaluation of the nature of the epithelial substratum throughout the course of limb regeneration are discussed.
将蝾螈绿红东美螈(Notophthalmus (Triturus) viridescens)的前肢在腕部截肢,在14至25天时,用剃须刀片切除新长出的肢体再生组织。将分离出的再生组织在仅含无机盐的培养基中孵育后,上皮组织很容易从下方的间充质中分离出来。在盐溶液中分离的表面用扫描电子显微镜和透射电子显微镜进行检查,以评估分离的完整性以及分离平面附近组织损伤的程度。很少发现有上皮细胞附着在间充质表面,这支持了之前的光学显微镜观察结果。最明显的形态学损伤发生在基底上皮细胞表面,表现为起泡;新暴露的质膜附近细胞质内形成空泡;一些细胞器的结构破坏;以及基底上皮细胞质膜碎片被撕裂,这些碎片在分离过程中仍附着在间充质表面。对完整再生组织上皮 - 间充质界面结构的检查表明,上皮 - 间充质分离平面大部分位于基底上皮细胞膜与其基质之间,这种细胞外物质在分离后留在间充质表面。这种基质呈细胞外物质的形式,在再生组织的远端紧密附着于基底上皮细胞膜;在经历芽基积累的再生组织周边是正在形成的基膜;或在指状阶段再生组织底部是成熟的基膜。讨论了这些分离组织在未来实验中的用途以及在肢体再生过程中对上皮基质性质的评估。