多能状态转换协调小鼠和人类胚胎的形态发生
Marta N Shahbazi1, Antonio Scialdone2, Natalia Skorupska1
1Mammalian Embryo and Stem Cell Group, University of Cambridge, Department of Physiology, Development and Neuroscience, Downing Street, Cambridge CB2 3EG, UK.
Nature
|November 30, 2017
概括
在哺乳动物胚胎发育过程中, 脱离纯粹的多能性至关重要. 这种转变使表皮质上皮质化和基本腔的形成成为可能,比如小鼠的亲胎腔和人类的胎腔.
科学领域:
- 发育生物学
- 干细胞生物学
- 细胞生物学
背景情况:
- 哺乳动物的发育源于经历表皮化过程的表皮细胞.
- 多能状态具有分子特征,但它们的发育作用尚不清楚.
- 表皮化和腔腔形成是早期发育的基本事件.
研究的目的:
- 研究哺乳动物胚胎发育过程中的多能状态的生物学意义.
- 确定退出纯粹多能状态在表皮质上皮质化和腔腔形成中的作用.
- 阐明分子机制,将多能性退出与光生成联系起来.
主要方法:
- 使用小鼠胚胎和培养后的人类胚胎.
- 使用胚胎干细胞来模拟纯粹的多能性.
- 分析了基因表达,蛋白质定位和组织形态.
主要成果:
- 在小鼠胚胎中,脱离原始多能性对于表皮质和亲胎腔形成至关重要.
- 胚胎干细胞在原始状态下可以两极分化,但不能形成光线.
- 从纯粹的多能性退出激活一个Oct4依赖的转录程序,导致氨酸表达和发光.
- 在人类胚胎中,出生的幼稚多能性会触发胚胎腔的形成和发育.
结论:
- 在哺乳动物发育过程中,多能状态之间的过渡对于建立组织结构至关重要.
- 多能性退出是发光和发展进展的先决条件.
- 组织层架构为定义多能状态提供了一个新的标准.
相关概念视频
Gastrulation
67.7K
Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of intricate cellular movements, which in humans transforms a flat, “bilaminar disc” composed of two cell sheets into a three-tiered structure. In the resulting embryo, the endoderm serves as the bottom layer, and stacked directly above it is the intermediate mesoderm, and then the uppermost ectoderm. Respectively, these tissue strata...
67.7K
Maintenance of the ES Cell State
2.8K
The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...
2.8K
Somatic to iPS Cell Reprogramming
2.7K
Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.7K
Forced Transdifferentiation
2.4K
Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
Artificial...
2.4K


