scholarly journals Is the time right for in vitro neurotoxicity testing using human iPSC-derived neurons?

ALTEX ◽  
2016 ◽  
Author(s):  
Anke Tukker
Keyword(s):  
2021 ◽  
Vol 52 ◽  
pp. 102206
Author(s):  
Alexandra Haase ◽  
Tim Kohrn ◽  
Veronika Fricke ◽  
Maria Elena Ricci Signorini ◽  
Merlin Witte ◽  
...  

2021 ◽  
Vol 111 ◽  
pp. 107050
Author(s):  
Michelangelo Paci ◽  
Jussi T. Koivumäki ◽  
Elisa Passini ◽  
Blanca Rodriguez
Keyword(s):  

Author(s):  
Felix Schmieder ◽  
Rouhollah Habibey ◽  
Volker Busskamp ◽  
Lars Büttner ◽  
Jürgen W. Czarske
Keyword(s):  

Author(s):  
Dinah Misner ◽  
Chelsea Snyder ◽  
Tin Ngo ◽  
Lanlan Yu ◽  
Nicola Stagg ◽  
...  
Keyword(s):  

2017 ◽  
Vol 25 ◽  
pp. 72-82 ◽  
Author(s):  
Maxi Hofrichter ◽  
Laura Nimtz ◽  
Julia Tigges ◽  
Yaschar Kabiri ◽  
Friederike Schröter ◽  
...  

2019 ◽  
Author(s):  
Ayshwarya Subramanian ◽  
Eriene-Heidi Sidhom ◽  
Maheswarareddy Emani ◽  
Nareh Sahakian ◽  
Katherine Vernon ◽  
...  

AbstractHuman iPSC-derived kidney organoids have the potential to revolutionize discovery, but assessing their consistency and reproducibility across iPSC lines, and reducing the generation of off-target cells remain an open challenge. Here, we used single cell RNA-Seq (scRNA-Seq) to profile 415,775 cells to show that organoid composition and development are comparable to human fetal and adult kidneys. Although cell classes were largely reproducible across iPSC lines, time points, protocols, and replicates, cell proportions were variable between different iPSC lines. Off-target cell proportions were the most variable. Prolonged in vitro culture did not alter cell types, but organoid transplantation under the mouse kidney capsule diminished off-target cells. Our work shows how scRNA-seq can help score organoids for reproducibility, faithfulness and quality, that kidney organoids derived from different iPSC lines are comparable surrogates for human kidney, and that transplantation enhances their formation by diminishing off-target cells.


Author(s):  
Subashika Govindan ◽  
Laura Batti ◽  
Samira F. Osterop ◽  
Luc Stoppini ◽  
Adrien Roux

Minibrain is a 3D brain in vitro spheroid model, composed of a mixed population of neurons and glial cells, generated from human iPSC derived neural stem cells. Despite the advances in human 3D in vitro models such as aggregates, spheroids and organoids, there is a lack of labeling and imaging methodologies to characterize these models. In this study, we present a step-by-step methodology to generate human minibrain nurseries and novel strategies to subsequently label projection neurons, perform immunohistochemistry and 3D imaging of the minibrains at large multiplexable scales. To visualize projection neurons, we adapt viral transduction and to visualize the organization of cell types we implement immunohistochemistry. To facilitate 3D imaging of minibrains, we present here pipelines and accessories for one step mounting and clearing suitable for confocal microscopy. The pipelines are specifically designed in such a way that the assays can be multiplexed with ease for large-scale screenings using minibrains and other organoid models. Using the pipeline, we present (i) dendrite morphometric properties obtained from 3D neuron morphology reconstructions, (ii) diversity in neuron morphology, and (iii) quantified distribution of progenitors and POU3F2 positive neurons in human minibrains.


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