NgR1 is an NK cell inhibitory receptor that destabilizes the immunological synapse

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dc.contributor.authorSe-Chan Oh-
dc.contributor.authorS E Kim-
dc.contributor.authorIn Hwan Jang-
dc.contributor.authorSeok-Min Kim-
dc.contributor.authorSoo Yun Lee-
dc.contributor.authorSunyoung Lee-
dc.contributor.authorIn-Sun Chu-
dc.contributor.authorSuk Ran Yoon-
dc.contributor.authorHaiyoung Jung-
dc.contributor.authorIn Pyo Choi-
dc.contributor.authorJ Doh-
dc.contributor.authorTae-Don Kim-
dc.date.accessioned2023-03-06T16:33:13Z-
dc.date.available2023-03-06T16:33:13Z-
dc.date.issued2023-
dc.identifier.issn1529-2908-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/31340-
dc.description.abstractThe formation of an immunological synapse (IS) is essential for natural killer (NK) cells to eliminate target cells. Despite an advanced understanding of the characteristics of the IS and its formation processes, the mechanisms that regulate its stability via the cytoskeleton are unclear. Here, we show that Nogo receptor 1 (NgR1) has an important function in modulating NK cell-mediated killing by destabilization of IS formation. NgR1 deficiency or blockade resulted in improved tumor control of NK cells by enhancing NK-to-target cell contact stability and regulating F-actin dynamics during IS formation. Patients with tumors expressing abundant NgR1 ligand had poor prognosis despite high levels of NK cell infiltration. Thus, our study identifies NgR1 as an immune checkpoint in IS formation and indicates a potential approach to improve the cytolytic function of NK cells in cancer immunotherapy.-
dc.publisherSpringer-Nature Pub Group-
dc.titleNgR1 is an NK cell inhibitory receptor that destabilizes the immunological synapse-
dc.title.alternativeNgR1 is an NK cell inhibitory receptor that destabilizes the immunological synapse-
dc.typeArticle-
dc.citation.titleNature Immunology-
dc.citation.number3-
dc.citation.endPage473-
dc.citation.startPage463-
dc.citation.volume24-
dc.contributor.affiliatedAuthorSe-Chan Oh-
dc.contributor.affiliatedAuthorIn Hwan Jang-
dc.contributor.affiliatedAuthorSeok-Min Kim-
dc.contributor.affiliatedAuthorSoo Yun Lee-
dc.contributor.affiliatedAuthorSunyoung Lee-
dc.contributor.affiliatedAuthorIn-Sun Chu-
dc.contributor.affiliatedAuthorSuk Ran Yoon-
dc.contributor.affiliatedAuthorHaiyoung Jung-
dc.contributor.affiliatedAuthorIn Pyo Choi-
dc.contributor.affiliatedAuthorTae-Don Kim-
dc.contributor.alternativeName오세찬-
dc.contributor.alternativeName김성은-
dc.contributor.alternativeName장인환-
dc.contributor.alternativeName김석민-
dc.contributor.alternativeName이수연-
dc.contributor.alternativeName이선영-
dc.contributor.alternativeName추인선-
dc.contributor.alternativeName윤석란-
dc.contributor.alternativeName정해용-
dc.contributor.alternativeName최인표-
dc.contributor.alternativeName도준상-
dc.contributor.alternativeName김태돈-
dc.identifier.bibliographicCitationNature Immunology, vol. 24, no. 3, pp. 463-473-
dc.identifier.doi10.1038/s41590-022-01394-w-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Aging Convergence Research Center > 1. Journal Articles
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