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自上而下抑制(TDi)与基线激活(BLa):当内源性细胞因子破坏你的分化时对信号转导的控制

Top-Down Inhibition (TDi) and Baseline Activation (BLa): Controlling Signal Transduction When Endogenous Cytokines are Ruining Your Differentiation.

作者信息

Hackland James

机构信息

Developmental Biology, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

Curr Protoc Stem Cell Biol. 2019 Dec;51(1):e98. doi: 10.1002/cpsc.98.

Abstract

In the 20 years since the first human pluripotent stem cell (hPSC) lines were established, there have been a plethora of protocols developed that allow us to generate a wide range of human cell types in vitro. Efforts to achieve a greater degree of specificity and efficiency in generating desired cell types have resulted in increasingly complex approaches. The magnitude and timing of signals has become key, and the concept of a "fully defined" system is a forever sought-after goal with shifting goalposts. This overview discusses two related approaches that can be used to deliver a tightly regulated, intermediate-strength signal, and which can also manage the impact of endogenous signaling variation and enable a switch away from bovine serum albumin-containing medium to a better-defined system without suffering a subsequent loss of robustness or efficiency. The approaches, referred to as top-down inhibition and baseline activation, were developed to deliver intermediate levels of BMP and WNT signaling during neural crest induction from hPSC, but could be applied to a variety of other signals and differentiation systems. © 2019 by John Wiley & Sons, Inc.

摘要

自首批人类多能干细胞(hPSC)系建立以来的20年里,已开发出大量方案,使我们能够在体外生成多种人类细胞类型。为了在生成所需细胞类型时实现更高程度的特异性和效率,人们采用了越来越复杂的方法。信号的强度和时机已成为关键,而“完全确定”系统的概念是一个目标不断变化、永远追求的目标。本综述讨论了两种相关方法,可用于传递严格调控的中等强度信号,还能管理内源性信号变化的影响,并能从含牛血清白蛋白的培养基转换到定义更明确的系统,而不会在后续出现稳健性或效率损失。这两种方法分别称为自上而下抑制和基线激活,最初是为了在从hPSC诱导神经嵴的过程中传递中等水平的BMP和WNT信号而开发的,但也可应用于多种其他信号和分化系统。© 2019约翰威立父子公司版权所有

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