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[美西螈轴中胚层胆碱酯酶的组织化学研究]

[A histochemical study of cholinesterase in the axial mesoderm ofTriturus cristatus].

作者信息

Kocher-Becker U, Drews U

机构信息

Heiligenberg-Institut, Deutschland.

Abteilung für Klinische Morphologie der Universität Ulm, Deutschland.

出版信息

Wilhelm Roux Arch Entwickl Mech Org. 1970 Jun;165(2):163-173. doi: 10.1007/BF00650144.

Abstract
  1. InTriturus cristatus embryos (Harrison stages 15-42) the development of cholinesterase (ChE) activity in the axial mesoderm was investigated. 2. After embedding in polyethylene glycol the histochemical technique of Karnovsky and Roots (preincubation in maleinimid to block sulfhydryl groups) and that of Koelle were employed on serial sections. 3. In early neurula stage ChE is found in the presumptive notochordal and somite material of the archenteron roof. 4. The notochord is ChE-positive from late neurula stage until Harrison stage 25. Then the cells loose their activity in cranio-caudal progression. 5. The subnotochordal rod is ChE-positive from Harrison stage 21/22 until Harrison stage 30-33. 6. The somites are ChE-positive as they develop. 7. During the formation of myotomes, beginning in the cranial part of the embryo the amount of ChE in the engaged somite cells increases. At this time (Harrison 24-26) ChE-negative somites are found in the caudal part of the embryo. These somites become ChE-positive before they change into myotomes. 8. From the beginning the whole myoblasts are ChE-positive. Beginning with Harrison stage 35 the activity concentrates at the ends of the myoblasts near the segmental border. At this time a strong activity in the motor cells of the neural tube appears.
摘要
  1. 在有尾蝾螈胚胎(哈里森第15 - 42期)中,研究了轴中胚层胆碱酯酶(ChE)活性的发育情况。2. 用聚乙二醇包埋后,对连续切片采用了卡诺夫斯基和鲁茨的组织化学技术(在马来酰亚胺中预孵育以阻断巯基)以及科尔的技术。3. 在神经胚早期,在原肠顶的预定脊索和体节物质中发现了ChE。4. 从神经胚晚期到哈里森第25期,脊索呈ChE阳性。然后细胞在头 - 尾方向上逐渐失去活性。5. 脊索下棒从哈里森第21/22期到哈里森第30 - 33期呈ChE阳性。6. 体节在发育过程中呈ChE阳性。7. 在肌节形成期间,从胚胎头部开始,参与的体节细胞中的ChE量增加。此时(哈里森第24 - 26期),在胚胎尾部发现ChE阴性的体节。这些体节在转变为肌节之前变为ChE阳性。8. 从一开始,整个成肌细胞就呈ChE阳性。从哈里森第35期开始,活性集中在成肌细胞靠近节段边界的末端。此时神经管的运动细胞出现强烈活性。

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