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正常及经睾酮处理的鸡胚的滑囊发育

Bursal development in normal and testosterone-treated chick embryos.

作者信息

Oláh I, Glick B, Törö I

出版信息

Poult Sci. 1986 Mar;65(3):574-88. doi: 10.3382/ps.0650574.

Abstract

The development of the bursa of Fabricius was studied in normal and testosterone-treated embryos. The bursal anlage appears on the 5th day of incubation as an outgrowth of the dorso-caudal wall of the cloaca. By Day 7, the bursal lumen is present and separated from the anal invagination by a thin epithelial membrane. Shortly after this developmental state, the epithelial membrane disappears and the bursal lumen freely communicates with the amniotic cavity. The remnant of the bursal anlage forms the ventral wall of the anal invagination that is actually the bursal duct. Disappearance of the remnant of the bursal anlage, which takes place after the 16th day of incubation, allows the bursa to join the cloaca. Bursal folds appear on the 10th day of incubation. Mesenchymal cells then differentiate into dark and light cells. The dark cells, between 11 and 14 days of incubation, mobilize in the mesenchymal network and assemble in small groups under the epithelial rudiment of the folds. They, then, enter the epithelium where they induce bud formation. During the assemblage of dark cells beneath the epithelium and their emigration into the epithelium, they acquire cytoplasmic granules that resemble avian secretory cells. The light cells do not associate with the epithelium. They may be the precursors of cortical reticular cells. The differentiation of dark cells is inhibited in the presence of testosterone. Therefore, the failure of bud formation and subsequent follicular formation in the bursa of testosterone-treated embryos may be attributed to the elimination of an induction signal supplied by the differentiated dark cells of the mesenchyme.

摘要

在正常胚胎和经睾酮处理的胚胎中研究了法氏囊的发育。法氏囊原基在孵化第5天作为泄殖腔背尾壁的一个突出物出现。到第7天,法氏囊腔存在,并通过一层薄的上皮膜与肛门内陷分开。在这个发育状态后不久,上皮膜消失,法氏囊腔与羊膜腔自由连通。法氏囊原基的残余部分形成肛门内陷的腹壁,实际上就是法氏囊管。法氏囊原基残余部分在孵化第16天后消失,使法氏囊与泄殖腔相连。法氏囊褶皱在孵化第10天出现。间充质细胞随后分化为深色细胞和浅色细胞。深色细胞在孵化的第11至14天,在间充质网络中移动,并在褶皱的上皮原基下小群聚集。然后,它们进入上皮,在那里诱导芽的形成。在深色细胞在上皮下聚集并迁移到上皮内的过程中,它们获得了类似于禽类分泌细胞的细胞质颗粒。浅色细胞不与上皮相关联。它们可能是皮质网状细胞的前体。在睾酮存在的情况下,深色细胞的分化受到抑制。因此,经睾酮处理的胚胎法氏囊中芽形成和随后滤泡形成的失败可能归因于间充质中分化的深色细胞提供的诱导信号的消除。

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