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The co-inhibitory receptor TIGIT regulates NK cell function and is upregulated in human intrahepatic CD56 bright NK cells.

Authors :
Ziegler AE
Fittje P
Müller LM
Ahrenstorf AE
Hagemann K
Hagen SH
Hess LU
Niehrs A
Poch T
Ravichandran G
Löbl SM
Padoan B
Brias S
Hennesen J
Richard M
Richert L
Peine S
Oldhafer KJ
Fischer L
Schramm C
Martrus G
Bunders MJ
Altfeld M
Lunemann S
Source :
Frontiers in immunology [Front Immunol] 2023 Feb 09; Vol. 14, pp. 1117320. Date of Electronic Publication: 2023 Feb 09 (Print Publication: 2023).
Publication Year :
2023

Abstract

The crosstalk between NK cells and their surrounding environment is enabled through activating and inhibitory receptors, which tightly control NK cell activity. The co-inhibitory receptor TIGIT decreases NK cell cytotoxicity and is involved in NK cell exhaustion, but has also been associated with liver regeneration, highlighting that the contribution of human intrahepatic CD56 <superscript>bright</superscript> NK cells in regulating tissue homeostasis remains incompletely understood. A targeted single-cell mRNA analysis revealed distinct transcriptional differences between matched human peripheral blood and intrahepatic CD56 <superscript>bright</superscript> NK cells. Multiparameter flow cytometry identified a cluster of intrahepatic NK cells with overlapping high expression of CD56, CD69, CXCR6, TIGIT and CD96. Intrahepatic CD56 <superscript>bright</superscript> NK cells also expressed significantly higher protein surface levels of TIGIT, and significantly lower levels of DNAM-1 compared to matched peripheral blood CD56 <superscript>bright</superscript> NK cells. TIGIT <superscript>+</superscript> CD56 <superscript>bright</superscript> NK cells showed diminished degranulation and TNF-α production following stimulation. Co-incubation of peripheral blood CD56 <superscript>bright</superscript> NK cells with human hepatoma cells or primary human hepatocyte organoids resulted in migration of NK cells into hepatocyte organoids and upregulation of TIGIT and downregulation of DNAM-1 expression, in line with the phenotype of intrahepatic CD56 <superscript>bright</superscript> NK cells. Intrahepatic CD56 <superscript>bright</superscript> NK cells represent a transcriptionally, phenotypically, and functionally distinct population of NK cells that expresses higher levels of TIGIT and lower levels of DNAM-1 than matched peripheral blood CD56 <superscript>bright</superscript> NK cells. Increased expression of inhibitory receptors by NK cells within the liver environment can contribute to tissue homeostasis and reduction of liver inflammation.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Ziegler, Fittje, Müller, Ahrenstorf, Hagemann, Hagen, Hess, Niehrs, Poch, Ravichandran, Löbl, Padoan, Brias, Hennesen, Richard, Richert, Peine, Oldhafer, Fischer, Schramm, Martrus, Bunders, Altfeld and Lunemann.)

Details

Language :
English
ISSN :
1664-3224
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
36845105
Full Text :
https://doi.org/10.3389/fimmu.2023.1117320