eLifeImmunologyPeer-reviewed journal article
Layilin Regulates Treg Motility and Suppressive Capacity in Skin
Victoire GouirandiD, Sean Clancy, Courtney E. MaconiD, Jose Valle, Mariela L. PauliiD, Hong-An Troung, Jarish N. CoheniD, Maxime KinetiD, Margaret M. LoweiD, Samuel J. LordiD, Kristen SkruberiD, Hobart W. HarrisiD, Esther KimiD, Isaac M. NeuhausiD, Karin ReifiD, Ali A. ZarriniD, R. Dyche MullinsiD, Michael D. RosenblumiD
Abstract
Regulatory T cells (Tregs) are essential for maintaining immune tolerance in both lymphoid and non-lymphoid tissues. We discovered that layilin, a C-type lectin receptor, is predominantly expressed on Tregs in skin. Layilin was highly expressed on a subset of clonally expanded effector Tregs in both healthy and psoriatic skin. Layilin expressing Tregs exhibited a transcriptional profile indicative of enhanced adhesion. Deletion of layilin in Tregs in vivo resulted in significantly attenuated skin inflammation. Mechanistically, layilin enhanced Treg adhesion via modulation of LFA-1, resulting in distinct cytoskeletal alterations consistent with enhanced focal adhesion and lamellipodia formation. Taken together, we define layilin as a critical regulator of Treg suppressive capacity through modulating motility and adhesion in a non-lymphoid tissue.
- organism: human
- assay: bulk RNA-seq
- research focus: host-pathogen & immune response
- research focus: cell signaling & trafficking
- approach: experimental assay
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 0th percentile
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