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人类脊索的发育。

The development of the human notochord.

机构信息

Department of Medical Biology, Section Clinical Anatomy & Embryology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

PLoS One. 2018 Oct 22;13(10):e0205752. doi: 10.1371/journal.pone.0205752. eCollection 2018.

DOI:10.1371/journal.pone.0205752
PMID:30346967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6197658/
Abstract

The notochord is a major regulator of embryonic patterning in vertebrates and abnormal notochordal development is associated with a variety of birth defects in man. Proper knowledge of the development of the human notochord, therefore, is important to understand the pathogenesis of these birth defects. Textbook descriptions vary significantly and seem to be derived from both human and animal data whereas the lack of references hampers verification of the presented data. Therefore, a verifiable and comprehensive description of the development of the human notochord is needed. Our analysis and three-dimensional (3D) reconstructions of 27 sectioned human embryos ranging from Carnegie Stage 8 to 15 (17-41 days of development), resulted in a comprehensive and verifiable new model of notochordal development. Subsequent to gastrulation, a transient group of cells briefly persists as the notochordal process which is incorporated into the endodermal roof of the gut while its dorsal side attaches to the developing neural tube. Then, the notochordal process embeds entirely into the endoderm, forming the epithelial notochordal plate, which remains intimately associated with the neural tube. Subsequently, the notochordal cells detach from the endoderm to form the definitive notochord, allowing the paired dorsal aortae to fuse between the notochord and the gut. We show that the formation of the notochordal process and plate proceeds in cranio-caudal direction. Moreover, in contrast to descriptions in the modern textbooks, we report that the formation of the definitive notochord in humans starts in the middle of the embryo, and proceeds in both cranial and caudal directions.

摘要

脊索是脊椎动物胚胎模式形成的主要调节者,脊索发育异常与人类多种出生缺陷有关。因此,正确了解人类脊索的发育对于理解这些出生缺陷的发病机制非常重要。教科书的描述差异很大,似乎既有来自人类的也有来自动物的数据,而缺乏参考文献则阻碍了对所呈现数据的验证。因此,需要一个可验证和全面的人类脊索发育描述。我们对 27 个人类胚胎进行了分析和三维(3D)重建,这些胚胎从卡内基阶段 8 到 15 (17-41 天的发育),得到了一个全面和可验证的新脊索发育模型。原肠胚形成后,短暂地有一群细胞作为脊索原基存在,脊索原基被纳入肠道的内胚层顶,而其背侧附着在正在发育的神经管上。然后,脊索原基完全嵌入内胚层,形成上皮脊索板,与神经管紧密相连。随后,脊索细胞从内胚层分离,形成最终的脊索,使成对的背主动脉在脊索和肠道之间融合。我们表明,脊索原基和板的形成是从头至尾进行的。此外,与现代教科书中的描述相反,我们报告说,人类最终脊索的形成始于胚胎的中部,并向头侧和尾侧两个方向进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/63706a6c5167/pone.0205752.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/a80e2a7562fb/pone.0205752.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/b67ebef4b71c/pone.0205752.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/67fdd20dde0e/pone.0205752.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/bd1f06a0a876/pone.0205752.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/2c8c08044ca5/pone.0205752.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/63706a6c5167/pone.0205752.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/a80e2a7562fb/pone.0205752.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/b67ebef4b71c/pone.0205752.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/67fdd20dde0e/pone.0205752.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/bd1f06a0a876/pone.0205752.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/2c8c08044ca5/pone.0205752.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd03/6197658/63706a6c5167/pone.0205752.g006.jpg

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