4.8 Article

Systematic single-cell pathway analysis to characterize early T cell activation

Journal

CELL REPORTS
Volume 41, Issue 8, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2022.111697

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Funding

  1. Intramural Research Program of the NIH
  2. National Heart, Lung, and Blood Institute [zia/hl006223, Z99 HL999999, 5R01-HG006137-07, 1U2CCA233285-01]

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This study developed a statistical framework for single-cell pathway analysis, demonstrated its effectiveness compared to commonly used methods, and identified regulatory mechanisms and pathway activity in T cells.
Pathway analysis is a key analytical stage in the interpretation of omics data, providing a powerful method for detecting alterations in cellular processes. We recently developed a sensitive and distribution-free statistical framework for multisample distribution testing, which we implement here in the open-source R package single-cell pathway analysis (SCPA). We demonstrate the effectiveness of SCPA over commonly used methods, generate a scRNA-seq T cell dataset, and characterize pathway activity over early cellular activation. This reveals regulatory pathways in T cells, including an intrinsic type I interferon system regulating T cell survival and a reliance on arachidonic acid metabolism throughout T cell activation. A systems-level characterization of pathway activity in T cells across multiple tissues also identifies alpha-defensin expression as a hallmark of bone-marrow-derived T cells. Overall, this work provides a widely applicable tool for single-cell pathway analysis and highlights regulatory mechanisms of T cells.

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