Exploring the dynamics and influencing factors of CD4 T cell activation using single-cell RNA-seq
iScience, ISSN: 2589-0042, Vol: 26, Issue: 9, Page: 107588
2023
- 7Citations
- 11Captures
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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.
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Metrics Details
- Citations7
- Citation Indexes7
- CrossRef5
- Captures11
- Readers11
- 11
Article Description
T cell activation is a key event in adaptive immunity. However, the dynamics and influencing factors of T cell activation remain unclear. Here, we analyzed CD4 T cells that were stimulated with anti-CD3/CD28 under several conditions to explore the factors affecting T cell activation. We found a stimulated T subset (HSP hi T) highly expressing heat shock proteins, which was derived from stimulated naive T. We identified and characterized inert T, a stimulated T cell subset in transitional state from resting T to activated T. Interestingly, resting CXCR4 low T responded to stimulation more efficiently than resting CXCR4 hi T. Furthermore, stimulation of CD4 T in the presence of CD8 T resulted in more effector T and more homogeneous expressions of CD25, supporting that presence of CD8 T reduces the extreme response of T cells, which can be explained by regulation of CD4 T activation through CD8 T-initiated cytokine signaling and FAS/FASLG signaling.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2589004223016656; http://dx.doi.org/10.1016/j.isci.2023.107588; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85168821200&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37646019; https://linkinghub.elsevier.com/retrieve/pii/S2589004223016656; https://dx.doi.org/10.1016/j.isci.2023.107588
Elsevier BV
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