Cited time in webofscience Cited time in scopus

Full metadata record

DC Field Value Language
dc.contributor.author Lee, Minji -
dc.contributor.author Lee, Eun Min -
dc.contributor.author Han, Seong Kyu -
dc.contributor.author Choi, Yoon Ha -
dc.contributor.author Kwon, Dong-il -
dc.contributor.author Choi, Hyobeen -
dc.contributor.author Lee, Kwanghwan -
dc.contributor.author Park, Eun Seo -
dc.contributor.author Rha, Min-Seok -
dc.contributor.author Joo, Dong Jin -
dc.contributor.author Shin, Eui-Cheol -
dc.contributor.author Kim, Sanguk -
dc.contributor.author Kim, Jong Kyoung -
dc.contributor.author Lee, You Jeong -
dc.date.accessioned 2021-01-22T07:10:42Z -
dc.date.available 2021-01-22T07:10:42Z -
dc.date.created 2020-09-16 -
dc.date.issued 2020-08 -
dc.identifier.issn 2041-1723 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/12693 -
dc.description.abstract Invariant natural killer T (iNKT), mucosal-associated invariant T (MAIT), and γδ T cells are innate T cells that acquire memory phenotype in the thymus and share similar biological characteristics. However, how their effector differentiation is developmentally regulated is still unclear. Here, we identify analogous effector subsets of these three innate T cell types in the thymus that share transcriptional profiles. Using single-cell RNA sequencing, we show that iNKT, MAIT and γδ T cells mature via shared, branched differentiation rather than linear maturation or TCR-mediated instruction. Simultaneous TCR clonotyping analysis reveals that thymic maturation of all three types is accompanied by clonal selection and expansion. Analyses of mice deficient of TBET, GATA3 or RORγt and additional in vivo experiments corroborate the predicted differentiation paths, while human innate T cells from liver samples display similar features. Collectively, our data indicate that innate T cells share effector differentiation processes in the thymus. © 2020, The Author(s). -
dc.language English -
dc.publisher Nature Research -
dc.title Single-cell RNA sequencing identifies shared differentiation paths of mouse thymic innate T cells -
dc.type Article -
dc.identifier.doi 10.1038/s41467-020-18155-8 -
dc.identifier.scopusid 2-s2.0-85089997110 -
dc.identifier.bibliographicCitation Nature Communications, v.11, no.1, pp.4367 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus GAMMA-DELTA T -
dc.subject.keywordPlus SEQ DATA -
dc.subject.keywordPlus DIVERSITY -
dc.subject.keywordPlus RECOGNITION -
dc.subject.keywordPlus REPERTOIRE -
dc.subject.keywordPlus REARRANGEMENT -
dc.subject.keywordPlus EXPRESSION -
dc.subject.keywordPlus MOLECULES -
dc.subject.keywordPlus IMMUNITY -
dc.subject.keywordPlus GATA-3 -
dc.citation.number 1 -
dc.citation.startPage 4367 -
dc.citation.title Nature Communications -
dc.citation.volume 11 -
Files in This Item:
000569862400012.pdf

000569862400012.pdf

기타 데이터 / 3.89 MB / Adobe PDF download
Appears in Collections:
Department of New Biology Laboratory of Single-Cell Genomics 1. Journal Articles

qrcode

  • twitter
  • facebook
  • mendeley

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

BROWSE