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 beta-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.

Expression of E-cadherin by CD8+ T cells promotes their invasion into biliary epithelial cells

Ronca, Vincenzo
Conceptualization
;
2024-01-01

Abstract

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 beta-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.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11699/83563
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