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A novel self-organizing embryonic stem cell system reveals signaling logic underlying the patterning of human ectoderm.


ABSTRACT: During development, the ectoderm is patterned by a combination of BMP and WNT signaling. Research in model organisms has provided substantial insight into this process; however, there are currently no systems in which to study ectodermal patterning in humans. Further, the complexity of neural plate border specification has made it difficult to transition from discovering the genes involved to deeper mechanistic understanding. Here, we develop an in vitro model of human ectodermal patterning, in which human embryonic stem cells self-organize to form robust and quantitatively reproducible patterns corresponding to the complete medial-lateral axis of the embryonic ectoderm. Using this platform, we show that the duration of endogenous WNT signaling is a crucial control parameter, and that cells sense relative levels of BMP and WNT signaling in making fate decisions. These insights allowed us to develop an improved protocol for placodal differentiation. Thus, our platform is a powerful tool for studying human ectoderm patterning and for improving directed differentiation protocols.This article has an associated 'The people behind the papers' interview.

SUBMITTER: Britton G 

PROVIDER: S-EPMC6826045 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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A novel self-organizing embryonic stem cell system reveals signaling logic underlying the patterning of human ectoderm.

Britton George G   Heemskerk Idse I   Hodge Rachel R   Qutub Amina A AA   Warmflash Aryeh A  

Development (Cambridge, England) 20191017 20


During development, the ectoderm is patterned by a combination of BMP and WNT signaling. Research in model organisms has provided substantial insight into this process; however, there are currently no systems in which to study ectodermal patterning in humans. Further, the complexity of neural plate border specification has made it difficult to transition from discovering the genes involved to deeper mechanistic understanding. Here, we develop an <i>in vitro</i> model of human ectodermal patterni  ...[more]

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