Expression of E-cadherin by CD8 + T cells promotes their invasion into biliary epithelial cells.
Scott P DaviesVincenzo RoncaGrace E WoottonNatalia M KrajewskaAmber G BozwardRemi FiancetteDaniel A PattenKatharina YankouskayaGary M ReynoldsSofia PatDaniel-Clement Osei-BordomNaomi RichardsonLiam M GroverChristopher J WestonYe Htun OoPublished in: Nature communications (2024)
The presence of CD8 + T cells in the cytoplasm of biliary epithelial cells (BEC) has been correlated with biliary damage associated with primary biliary cholangitis (PBC). Here, we characterise the mechanism of CD8 + T cell invasion into BEC. CD8 + T cells observed within BEC were large, eccentric, and expressed E-cadherin, CD103 and CD69. They were also not contained within secondary vesicles. Internalisation required cytoskeletal rearrangements which facilitated contact with BEC. Internalised CD8 + T cells were observed in both non-cirrhotic and cirrhotic diseased liver tissues but enriched in PBC patients, both during active disease and at the time of transplantation. E-cadherin expression by CD8 + T cells correlated with frequency of internalisation of these cells into BEC. E-cadherin + CD8 + T cells formed β-catenin-associated interactions with BEC, were larger than E-cadherin - CD8 + T cells and invaded into BEC more frequently. Overall, we unveil a distinct cell-in-cell structure process in the liver detailing the invasion of E-cadherin + CD103 + CD69 + CD8 + T cells into BEC.
Keyphrases
- poor prognosis
- end stage renal disease
- single cell
- induced apoptosis
- gene expression
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- epithelial mesenchymal transition
- oxidative stress
- cell migration
- stem cells
- long non coding rna
- cell death
- cell proliferation
- bone marrow
- cell cycle arrest
- binding protein
- nk cells
- signaling pathway
- resistance training
- patient reported