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The Human Dendritic Cell Atlas: An Integrated Transcriptional Tool to Study Human Dendritic Cell Biology. | LitMetric

The Human Dendritic Cell Atlas: An Integrated Transcriptional Tool to Study Human Dendritic Cell Biology.

J Immunol

Department of Anatomy and Physiology, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Parkville, Victoria, Australia.

Published: December 2022

AI Article Synopsis

  • Dendritic cells (DCs) play diverse roles in various tissues but are challenging to study due to their low circulation and short lifespan.
  • Researchers created a transcriptional atlas of human DCs using data from multiple studies, revealing gene expression variations based on tissue types and responses to infections.
  • The atlas highlights differences between DCs generated in lab environments and those found in the body, serving as a valuable resource for understanding DC biology and developing better in vitro models.

Article Abstract

Dendritic cells (DCs) are functionally diverse and are present in most adult tissues, but deep understanding of human DC biology is hampered by relatively small numbers of these in circulation and their short lifespan in human tissues. We built a transcriptional atlas of human DCs by combining samples from 14 expression profiling studies derived from 10 laboratories. We identified significant gene expression variation of DC subset-defining markers across tissue type and upon viral or bacterial stimulation. We further highlight critical gaps between in vitro-derived DC subsets and their in vivo counterparts and provide evidence that monocytes or cord blood progenitor in vitro-differentiated DCs fail to capture the repertoire of primary DC subsets or behaviors. In constructing a reference DC atlas, we provide an important resource for the community wishing to identify and annotate tissue-specific DC subsets from single-cell datasets, or benchmark new in vitro models of DC biology.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719841PMC
http://dx.doi.org/10.4049/jimmunol.2200366DOI Listing

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