Cell metabolism: Functional and phenotypic single cell approaches
Methods in Cell Biology, ISSN: 0091-679X, Vol: 186, Page: 151-187
2024
- 1Citations
- 2Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations1
- Citation Indexes1
- Captures2
- Readers2
Article Description
Several metabolic pathways are essential for the physiological regulation of immune cells, but their dysregulation can cause immune dysfunction. Hypermetabolic and hypometabolic states represent deviations in the magnitude and flexibility of effector cells in different contexts, for example in autoimmunity, infections or cancer. To study immunometabolism, most methods focus on bulk populations and rely on in vitro activation assays. Nowadays, thanks to the development of single-cell technologies, including multiparameter flow cytometry, mass cytometry, RNA cytometry, among others, the metabolic state of individual immune cells can be measured in a variety of samples obtained in basic, translational and clinical studies. Here, we provide an overview of different single-cell approaches that are employed to investigate both mitochondrial functions and cell dependence from mitochondria metabolism. Moreover, besides the description of the appropriate experimental settings, we discuss the strengths and weaknesses of different approaches with the aim to suggest how to study cell metabolism in the settings of interest.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0091679X24000554; http://dx.doi.org/10.1016/bs.mcb.2024.02.024; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85188937378&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38705598; https://linkinghub.elsevier.com/retrieve/pii/S0091679X24000554; https://dx.doi.org/10.1016/bs.mcb.2024.02.024
Elsevier BV
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