BROWSE

ITEM VIEW & DOWNLOAD

Identification of a distinct NK-like hepatic T-cell population activated by NKG2C in a TCR-independent manner

DC Field Value Language
dc.contributor.authorKoh, June-Young-
dc.contributor.authorRha, Min-Seok-
dc.contributor.authorChoi, Seong Jin-
dc.contributor.authorLee, Ha Seok-
dc.contributor.authorHan, Ji Won-
dc.contributor.authorNam, Heejin-
dc.contributor.authorKim, Dong-Uk-
dc.contributor.authorLee, Jae Geun-
dc.contributor.authorKim, Myoung Soo-
dc.contributor.authorPark, Jun Yong-
dc.contributor.authorPark, Su-Hyung-
dc.contributor.authorJoo, Dong Jin-
dc.contributor.authorEui-Cheol Shin-
dc.date.accessioned2023-01-27T00:39:06Z-
dc.date.available2023-01-27T00:39:06Z-
dc.date.created2022-08-01-
dc.date.issued2022-10-
dc.identifier.issn0168-8278-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/12831-
dc.description.abstractBackground & Aims: The liver provides a unique niche of lymphocytes enriched with a large proportion of innate-like T cells. However, the heterogeneity and functional characteristics of the hepatic T-cell population remain to be fully elucidated. Methods: We obtained liver sinusoidal mononuclear cells from the liver perfusate of healthy donors and recipients with HBV-associated chronic liver disease (CLD) during liver transplantation. We performed a CITE-seq analysis of liver sinusoidal CD45+ cells in combination with T cell receptor (TCR)-seq and flow cytometry to examine the phenotypes and functions of liver sinusoidal CD8+ T cells. Results: We identified a distinct CD56hiCD161-CD8+ T-cell population characterized by natural killer (NK)-related gene expression and a uniquely restricted TCR repertoire. The frequency of these cells among the liver sinusoidal CD8+ T-cell population was significantly increased in patients with HBV-associated CLD. Although CD56hiCD161-CD8+ T cells exhibit weak responsiveness to TCR stimulation, CD56hiCD161-CD8+ T cells highly expressed various NK receptors, including CD94, killer immunoglobulin-like receptors, and NKG2C, and exerted NKG2C-mediated NK-like effector functions even in the absence of TCR stimulation. In addition, CD56hiCD161-CD8+ T cells highly respond to innate cytokines, such as IL-12/18 and IL-15, in the absence of TCR stimulation. We validated the results from liver sinusoidal CD8+ T cells using intrahepatic CD8+ T cells obtained from liver tissues. Conclusions: In summary, the current study found a distinct CD56hiCD161-CD8+ T-cell population characterized by NK-like activation via TCR-independent NKG2C ligation. Further studies are required to elucidate the roles of liver sinusoidal CD56hiCD161-CD8+ T cells in immune responses to microbial pathogens or liver immunopathology. Lay summary: The role of different immune cell populations in the liver is becoming an area of increasing interest. Herein, we identified a distinct T-cell population that had features similar to those of natural killer (NK) cells – a type of innate immune cell. This distinct population was expanded in the livers of patients with chronic liver disease and could thus have pathogenic relevance.-
dc.language영어-
dc.publisherElsevier B.V.-
dc.titleIdentification of a distinct NK-like hepatic T-cell population activated by NKG2C in a TCR-independent manner-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000868321600020-
dc.identifier.scopusid2-s2.0-85134624263-
dc.identifier.rimsid78670-
dc.contributor.affiliatedAuthorEui-Cheol Shin-
dc.identifier.doi10.1016/j.jhep.2022.05.020-
dc.identifier.bibliographicCitationJournal of Hepatology, v.77, no.4, pp.1059 - 1070-
dc.relation.isPartOfJournal of Hepatology-
dc.citation.titleJournal of Hepatology-
dc.citation.volume77-
dc.citation.number4-
dc.citation.startPage1059-
dc.citation.endPage1070-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusNATURAL-KILLER-CELLS-
dc.subject.keywordPlusSURFACE EXPRESSION-
dc.subject.keywordPlusHUMAN LIVER-
dc.subject.keywordPlusIMMUNE-RESPONSES-
dc.subject.keywordPlusMEMORY-
dc.subject.keywordPlusIL-15-
dc.subject.keywordPlusLYMPHOCYTES-
dc.subject.keywordPlusCYTOKINE-
dc.subject.keywordPlusSUBSETS-
dc.subject.keywordPlusINJURY-
dc.subject.keywordAuthorCD8+ T cell-
dc.subject.keywordAuthorCITE-seq-
dc.subject.keywordAuthorliver-
dc.subject.keywordAuthorNK cell receptor-
dc.subject.keywordAuthorNK-like T cell-
dc.subject.keywordAuthorNKG2C-
Appears in Collections:
Korea Virus Research Institute(한국바이러스기초연구소) > Center for Viral Immunology(바이러스 면역 연구센터) > 1. Journal Papers (저널논문)
Files in This Item:
There are no files associated with this item.

qrcode

  • facebook

    twitter

  • Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse