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  4. An automated do-it-yourself system for dynamic stem cell and organoid culture in standard multi-well plates
 
research article

An automated do-it-yourself system for dynamic stem cell and organoid culture in standard multi-well plates

Tischler, Julia  
•
Swank, Zoe  
•
Hsiung, Hao-An  
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July 18, 2022
Cell Reports Methods

We present a low-cost, do-it-yourself system for complexmammalian cell culture under dynamically changing medium formulations by integrating conventional multi-well tissue culture plates with simple microfluidic control and system automation. We demonstrate the generation of complex concentration profiles, enabling the investigation of sophisticated input-response relations. We further apply our automated cell-culturing platform to the dynamic stimulation of two widely employed stem-cell-based in vitro models for early mammalian development: the conversion of naivemouse embryonic stemcells into epiblast-like cells andmouse 3Dgastruloids. Performing automatedmedium-switch experiments, we systematically investigate cell fate commitment along the developmental trajectory toward mouse epiblast fate and examine symmetry-breaking, germ layer formation, and cardiac differentiation in mouse 3D gastruloids as a function of time-varyingWnt pathway activation. With these proof-of-principle examples, we demonstrate a highly versatile and scalable tool that can be adapted to specific research questions, experimental demands, and model systems.

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Type
research article
DOI
10.1016/j.crmeth.2022.100244
Web of Science ID

WOS:000907944100004

Author(s)
Tischler, Julia  
Swank, Zoe  
Hsiung, Hao-An  
Vianello, Stefano  
Lutolf, Matthias P.  
Maerkl, Sebastian J.  
Date Issued

2022-07-18

Published in
Cell Reports Methods
Volume

2

Issue

7

Article Number

100244

Subjects

Biochemical Research Methods

•

Cell Biology

•

Biochemistry & Molecular Biology

•

Cell Biology

•

ground-state

•

generation

•

specification

•

pluripotency

•

entrainment

•

gastruloids

•

transition

•

pathway

•

signals

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LBNC  
Available on Infoscience
February 13, 2023
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/194808
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