scholarly journals Multiplexing Spheroid Volume, Resazurin and Acid Phosphatase Viability Assays for High-Throughput Screening of Tumour Spheroids and Stem Cell Neurospheres

PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e103817 ◽  
Author(s):  
Delyan P. Ivanov ◽  
Terry L. Parker ◽  
David A. Walker ◽  
Cameron Alexander ◽  
Marianne B. Ashford ◽  
...  
Marine Drugs ◽  
2020 ◽  
Vol 18 (4) ◽  
pp. 192
Author(s):  
Pietro Marchese ◽  
Nipun Mahajan ◽  
Enda O’Connell ◽  
Howard Fearnhead ◽  
Maria Tuohy ◽  
...  

Worldwide diffused diseases such as osteoarthritis, atherosclerosis or chronic kidney disease are associated with a tissue calcification process which may involve unexpected local stem cell differentiation. Current pharmacological treatments for such musculoskeletal conditions are weakly effective, sometimes extremely expensive and often absent. The potential to develop new therapies is represented by the discovery of small molecules modulating resident progenitor cell differentiation to prevent aberrant tissue calcification. The marine environment is a rich reserve of compounds with pharmaceutical potential and many novel molecules are isolated from macro and microorganisms annually. The potential of small molecules synthetized by marine filamentous fungi to influence the osteogenic and chondrogenic differentiation of human mesenchymal stem/stromal cells (hMSCs) was investigated using a novel, high-throughput automated screening platform. Metabolites synthetized by the marine-derived fungus Penicillium antarcticum were evaluated on the platform. Itaconic acid derivatives were identified as inhibitors of calcium elaboration into the matrix of osteogenically differentiated hMSCs and also inhibited hMSC chondrogenic differentiation, highlighting their capacity to impair ectopic calcification. Bioactive small molecule discovery is critical to address ectopic tissue calcification and the use of biologically relevant assays to identify naturally occurring metabolites from marine sources represents a strategy that can contribute to this effort.


2020 ◽  
Vol 335 ◽  
pp. 108627 ◽  
Author(s):  
Madel Durens ◽  
Jonathan Nestor ◽  
Madeline Williams ◽  
Kevin Herold ◽  
Robert F. Niescier ◽  
...  

2015 ◽  
Vol 28 (7) ◽  
pp. 1472-1476 ◽  
Author(s):  
Yacoub Y. I. Amin ◽  
Kasper Runager ◽  
Fabio Simoes ◽  
Adam Celiz ◽  
Vincenzo Taresco ◽  
...  

2008 ◽  
Vol 36 (11) ◽  
pp. 1909-1921 ◽  
Author(s):  
Alice H. Huang ◽  
Nuzhat A. Motlekar ◽  
Ashley Stein ◽  
Scott L. Diamond ◽  
Eileen M. Shore ◽  
...  

2013 ◽  
Vol 236 ◽  
pp. 35-47 ◽  
Author(s):  
Brittni A. Scruggs ◽  
Annie C. Bowles ◽  
Xiujuan Zhang ◽  
Julie A. Semon ◽  
Evan J. Kyzar ◽  
...  

2020 ◽  
Author(s):  
Naoya Kase ◽  
Madoka Terashima ◽  
Akira Ohta ◽  
Akira Niwa ◽  
Fumiko Honda-Ozaki ◽  
...  

AbstractNakajo-Nishimura syndrome (NNS) is an autoinflammatory disorder caused by a homozygous mutations in PSMB8 gene. The administration of systemic corticosteroids is partially effective, but continuous treatment causes severe side effects. We previously established a pluripotent stem cell (PSC)-derived NNS disease model that reproduces several inflammatory phenotypes including the overproduction of monocyte chemoattractant protein-1 (MCP-1) and interferon gamma-induced protein-10 (IP-10). Here we performed high-throughput compound screening (HTS) using this PSC-derived NNS model to find potential therapeutic candidates and identified CUDC-907 as an effective inhibitor of the release of MCP-1 and IP-10. CUDC-907 did not induce cell death within therapeutic concentrations and was also effective on primary patient cells. Further analysis indicated that the inhibitory effect was post-transcriptional. These findings suggest that HTS with PSC-derived disease models is useful for finding drug candidates for autoinflammatory diseases.Significance statementIn this study, we identified a histone deacetylase inhibitor CUDC-907 as a potential effective compound for ameliorating overproduction of inflammatory chemokines in an autoinflammatory disease named Nakajo-Nishimura syndrome. We performed high-throughput screening using pluripotent stem cell-derived monocytic cell lines. Our data prove the validity of screening system as a versatile platform for seeking candidate compounds for the treatment of congenital immunological disorders associated with monocytic lineage cells.


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