Hackland James
Developmental Biology, Memorial Sloan Kettering Cancer Center, New York, New York.
Curr Protoc Stem Cell Biol. 2019 Dec;51(1):e98. doi: 10.1002/cpsc.98.
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.
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