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Transcriptional space-time mapping identifies concerted immune and stromal cell patterns and gene programs in wound healing and cancer. | LitMetric

Transcriptional space-time mapping identifies concerted immune and stromal cell patterns and gene programs in wound healing and cancer.

Cell Stem Cell

Department of Pathology, University of California, San Francisco, San Francisco, CA 94143, USA; ImmunoX Initiative, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address:

Published: June 2023

AI Article Synopsis

  • Scientists studied how different cells work together to heal skin wounds over time.
  • They discovered patterns in how genes are turned on and off during this healing process, which they called "movements."
  • They also found similar healing patterns in tumors, suggesting that tumors behave like wounds that don’t completely heal.

Article Abstract

Tissue repair responses in metazoans are highly coordinated by different cell types over space and time. However, comprehensive single-cell-based characterization covering this coordination is lacking. Here, we captured transcriptional states of single cells over space and time during skin wound closure, revealing choreographed gene-expression profiles. We identified shared space-time patterns of cellular and gene program enrichment, which we call multicellular "movements" spanning multiple cell types. We validated some of the discovered space-time movements using large-volume imaging of cleared wounds and demonstrated the value of this analysis to predict "sender" and "receiver" gene programs in macrophages and fibroblasts. Finally, we tested the hypothesis that tumors are like "wounds that never heal" and found conserved wound healing movements in mouse melanoma and colorectal tumor models, as well as human tumor samples, revealing fundamental multicellular units of tissue biology for integrative studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10843988PMC
http://dx.doi.org/10.1016/j.stem.2023.05.001DOI Listing

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