001     299797
005     20250511020436.0
024 7 _ |a 10.1093/jimmun/vkaf001
|2 doi
024 7 _ |a pmid:40079843
|2 pmid
024 7 _ |a 0022-1767
|2 ISSN
024 7 _ |a 1047-7381
|2 ISSN
024 7 _ |a 1048-3233
|2 ISSN
024 7 _ |a 1550-6606
|2 ISSN
024 7 _ |a altmetric:175246265
|2 altmetric
037 _ _ |a DKFZ-2025-00552
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Abe, Shinya
|b 0
245 _ _ |a The transcription factor RORα is required for the development of type 1 innate lymphoid cells in adult bone marrow.
260 _ _ |a Rockville, Md.
|c 2025
|b American Association of Immunologists
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1746619280_3746
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
500 _ _ |a 2025 Apr 1;214(4):575-581
520 _ _ |a Type 1 innate lymphoid cells (ILC1s) respond to infections and tumors by producing IFN-γ. Although RAR-related orphan receptor α (RORα) is required for ILC2s and some ILC3s, its role in ILC1 development remains controversial. To investigate the role of RORα in ILC1s, we analyzed bone marrow (BM) chimeras of RORα-deficient mice. ILC1s derived from RORα-deficient BM cells were significantly reduced in various tissues, including the intestine, indicating a hematopoietic cell-intrinsic need for RORα in ILC1 development. Developmental stage-specific RORα-deficient mice showed a decrease in adult liver and BM IL-7R+ ILC1s and an increase in BM NK cells, whereas fetal liver ILC1s and adult liver IL-7R- ILC1s remained unchanged. Furthermore, RORα is primarily required for IL-7R+ precursor stages and partially affects small intestine ILC1 after differentiation. This study suggests that RORα promotes ILC1 differentiation while suppressing NK cell differentiation at the ILC precursor stage in the adult BM.
536 _ _ |a 314 - Immunologie und Krebs (POF4-314)
|0 G:(DE-HGF)POF4-314
|c POF4-314
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |a RORα
|2 Other
650 _ 7 |a group 1 ILC
|2 Other
650 _ 7 |a innate lymphoid precursor
|2 Other
650 _ 7 |a type 1 innate lymphoid cell
|2 Other
700 1 _ |a Kagao, Moe
|b 1
700 1 _ |a Asahi, Takuma
|0 0000-0001-6372-7563
|b 2
700 1 _ |a Kato, Ryoma
|b 3
700 1 _ |a Tani-Ichi, Shizue
|0 0000-0003-2388-776X
|b 4
700 1 _ |a Shimba, Akihiro
|b 5
700 1 _ |a Ishibashi, Riki
|b 6
700 1 _ |a Miyachi, Hitoshi
|0 0000-0002-4855-3857
|b 7
700 1 _ |a Kitano, Satsuki
|b 8
700 1 _ |a Miyazaki, Masaki
|0 0000-0002-9543-624X
|b 9
700 1 _ |a Rodewald, Hans-Reimer
|0 P:(DE-He78)86fa3316b7be0d661065d02b3baec3d6
|b 10
|u dkfz
700 1 _ |a Toyoshima, Fumiko
|0 0000-0002-3698-0034
|b 11
700 1 _ |a Ikuta, Koichi
|0 0000-0003-1319-1021
|b 12
773 _ _ |a 10.1093/jimmun/vkaf001
|g p. vkaf001
|0 PERI:(DE-600)1475085-5
|n 4
|p 575-581
|t The journal of immunology
|v 214
|y 2025
|x 0022-1767
909 C O |p VDB
|o oai:inrepo02.dkfz.de:299797
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 10
|6 P:(DE-He78)86fa3316b7be0d661065d02b3baec3d6
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-314
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Immunologie und Krebs
|x 0
914 1 _ |y 2025
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2025-01-07
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2025-01-07
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b J IMMUNOL : 2022
|d 2025-01-07
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
|d 2025-01-07
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
|d 2025-01-07
915 _ _ |a IF < 5
|0 StatID:(DE-HGF)9900
|2 StatID
|d 2025-01-07
920 1 _ |0 I:(DE-He78)D110-20160331
|k D110
|l Zelluläre Immunologie
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)D110-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21