scholarly journals High-Throughput Screening Enhances Kidney Organoid Differentiation from Human Pluripotent Stem Cells and Enables Automated Multidimensional Phenotyping

2018 ◽  
Vol 22 (6) ◽  
pp. 929-940.e4 ◽  
Author(s):  
Stefan M. Czerniecki ◽  
Nelly M. Cruz ◽  
Jennifer L. Harder ◽  
Rajasree Menon ◽  
James Annis ◽  
...  
2012 ◽  
Vol 9 (3) ◽  
pp. 192-195 ◽  
Author(s):  
Riikka J. Lund ◽  
Tuomas Nikula ◽  
Nelly Rahkonen ◽  
Elisa Närvä ◽  
Duncan Baker ◽  
...  

2016 ◽  
Vol 16 (3) ◽  
pp. 640-650 ◽  
Author(s):  
Arnaud Carpentier ◽  
Ila Nimgaonkar ◽  
Virginia Chu ◽  
Yuchen Xia ◽  
Zongyi Hu ◽  
...  

2020 ◽  
Vol 7 (3) ◽  
pp. 92
Author(s):  
Mariana A. Branco ◽  
Joaquim M.S. Cabral ◽  
Maria Margarida Diogo

The knowledge acquired throughout the years concerning the in vivo regulation of cardiac development has promoted the establishment of directed differentiation protocols to obtain cardiomyocytes (CMs) and other cardiac cells from human pluripotent stem cells (hPSCs), which play a crucial role in the function and homeostasis of the heart. Among other developments in the field, the transition from homogeneous cultures of CMs to more complex multicellular cardiac microtissues (MTs) has increased the potential of these models for studying cardiac disorders in vitro and for clinically relevant applications such as drug screening and cardiotoxicity tests. This review addresses the state of the art of the generation of different cardiac cells from hPSCs and the impact of transitioning CM differentiation from 2D culture to a 3D environment. Additionally, current methods that may be employed to generate 3D cardiac MTs are reviewed and, finally, the adoption of these models for in vitro applications and their adaptation to medium- to high-throughput screening settings are also highlighted.


2021 ◽  
Vol 30 (161) ◽  
pp. 210042
Author(s):  
Pien A. Goldsteen ◽  
Christina Yoseif ◽  
Amalia M. Dolga ◽  
Reinoud Gosens

Respiratory diseases are among the leading causes of morbidity and mortality worldwide, representing a major unmet medical need. New chemical entities rarely make it into the clinic to treat respiratory diseases, which is partially due to a lack of adequate predictive disease models and the limited availability of human lung tissues to model respiratory disease. Human pluripotent stem cells (hPSCs) may help fill this gap by serving as a scalable human in vitro model. In addition, human in vitro models of rare genetic mutations can be generated using hPSCs. hPSC-derived epithelial cells and organoids have already shown great potential for the understanding of disease mechanisms, for finding new potential targets by using high-throughput screening platforms, and for personalised treatments. These potentials can also be applied to other hPSC-derived lung cell types in the future. In this review, we will discuss how hPSCs have brought, and may continue to bring, major changes to the field of respiratory diseases by understanding the molecular mechanisms of the pathology and by finding efficient therapeutics.


2013 ◽  
Vol 137 (1) ◽  
pp. 76-90 ◽  
Author(s):  
Sei Kameoka ◽  
Joshua Babiarz ◽  
Kyle Kolaja ◽  
Eric Chiao

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