دورية أكاديمية
Cellular, Molecular, and Immunological Characteristics of Langhans Multinucleated Giant Cells Programmed by IL-15.
العنوان: | Cellular, Molecular, and Immunological Characteristics of Langhans Multinucleated Giant Cells Programmed by IL-15. |
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المؤلفون: | Wang H; Department of Medicine, Division of Dermatology, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA; Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China., Jiang H; Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China., Teles RMB; Department of Medicine, Division of Dermatology, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA., Chen Y; Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China., Wu A; Suzhou Institute of Systems Medicine Center of Systems Medicine, Chinese Academy of Medical Sciences, Suzhou, China., Lu J; Department of Molecular, Cell and Developmental Biology, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA., Chen Z; Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China., Ma F; Department of Molecular, Cell and Developmental Biology, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA., Pellegrini M; Department of Molecular, Cell and Developmental Biology, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA., Modlin RL; Department of Medicine, Division of Dermatology, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA; Department of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California (UCLA), Los Angeles, California, USA. Electronic address: rmodlin@mednet.ucla.edu. |
المصدر: | The Journal of investigative dermatology [J Invest Dermatol] 2020 Sep; Vol. 140 (9), pp. 1824-1836.e7. Date of Electronic Publication: 2020 Feb 22. |
نوع المنشور: | Journal Article; Research Support, Non-U.S. Gov't |
اللغة: | English |
بيانات الدورية: | Publisher: Elsevier Country of Publication: United States NLM ID: 0426720 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1523-1747 (Electronic) Linking ISSN: 0022202X NLM ISO Abbreviation: J Invest Dermatol Subsets: MEDLINE |
أسماء مطبوعة: | Publication: 2016- : New York : Elsevier Original Publication: Baltimore, Williams & Wilkins. |
مواضيع طبية MeSH: | Macrophage Activation*, Giant Cells, Langhans/*immunology , Interleukin-15/*metabolism, Cell Communication/immunology ; Cells, Cultured ; Gene Regulatory Networks/immunology ; Giant Cells, Langhans/metabolism ; Humans ; Interferon-gamma/metabolism ; Primary Cell Culture ; RNA-Seq ; Signal Transduction/genetics ; Signal Transduction/immunology ; T-Lymphocytes/immunology ; T-Lymphocytes/metabolism ; Transcriptome/immunology |
مستخلص: | Langhans multinucleated giant cells (LGCs) are a specific type of multinucleated giant cell containing a characteristic horseshoe-shaped ring of nuclei that are present within granulomas of infectious etiology. Although cytokines that trigger macrophage activation (such as IFN-γ) induce LGC formation, it is not clear whether cytokines that trigger macrophage differentiation contribute to LGC formation. Here, we found that IL-15, a cytokine that induces M1 macrophage differentiation, programs human peripheral blood adherent cells to form LGCs. Analysis of the IL-15‒treated adherent cell transcriptome identified gene networks for T cells, DNA damage and replication, and IFN-inducible genes that correlated with IL-15 treatment and LGC-type multinucleated giant cell formation. Gene networks enriched for myeloid cells were anticorrelated with IL-15 treatment and LGC formation. Functional studies revealed that T cells were required for IL-15‒induced LGC formation, involving a direct contact with myeloid cells through CD40L-CD40 interaction and IFN-γ release. These data indicate that IL-15 induces LGC formation through the direct interaction of activated T cells and myeloid cells. (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.) |
References: | Blood. 1985 Dec;66(6):1241-6. (PMID: 3933591) J Immunol. 1997 Jan 15;158(2):800-6. (PMID: 8992997) Bioinformatics. 2009 Apr 15;25(8):1091-3. (PMID: 19237447) Cell Host Microbe. 2009 Oct 22;6(4):343-53. (PMID: 19837374) Infect Immun. 2001 Feb;69(2):810-5. (PMID: 11159972) J Immunol. 1993 Apr 1;150(7):3002-10. (PMID: 8454870) Science. 2013 Mar 22;339(6126):1448-53. (PMID: 23449998) Proc Natl Acad Sci U S A. 1984 Jul;81(14):4554-7. (PMID: 6431409) Int J Lepr Other Mycobact Dis. 1966 Jul-Sep;34(3):255-73. (PMID: 5950347) Lab Invest. 1994 Nov;71(5):737-44. (PMID: 7967525) J Immunol. 2007 Mar 1;178(5):3161-9. (PMID: 17312164) Am J Respir Cell Mol Biol. 1992 Jan;6(1):57-62. (PMID: 1728295) BMC Genomics. 2017 Oct 25;18(1):824. (PMID: 29070035) Curr Opin Hematol. 2009 Jan;16(1):53-7. (PMID: 19057205) J Pathol. 1978 Nov;126(3):125-48. (PMID: 370353) Am J Pathol. 1995 Nov;147(5):1487-99. (PMID: 7485411) Sci Transl Med. 2014 Aug 20;6(250):250ra114. (PMID: 25143364) Nat Med. 2005 Jun;11(6):653-60. (PMID: 15880118) J Immunol. 2007 Apr 15;178(8):5245-52. (PMID: 17404308) J Immunol. 2008 Nov 15;181(10):7115-20. (PMID: 18981132) Sci Immunol. 2018 Aug 31;3(26):. (PMID: 30171080) Proc Natl Acad Sci U S A. 2007 Sep 4;104(36):14436-41. (PMID: 17726108) Cell. 2016 Nov 17;167(5):1264-1280.e18. (PMID: 28084216) Immunobiology. 2007;212(9-10):785-93. (PMID: 18086379) J Leukoc Biol. 2001 Sep;70(3):386-94. (PMID: 11527988) Int Immunol. 2012 Jan;24(1):5-15. (PMID: 22058328) Science. 1991 Oct 11;254(5029):277-9. (PMID: 1925582) BMC Bioinformatics. 2008 Dec 29;9:559. (PMID: 19114008) Adv Exp Med Biol. 2011;713:97-111. (PMID: 21432016) J Exp Med. 1989 May 1;169(5):1565-81. (PMID: 2523952) |
معلومات مُعتمدة: | R01 AI022553 United States AI NIAID NIH HHS; R01 AR040312 United States AR NIAMS NIH HHS; R01 AR073252 United States AR NIAMS NIH HHS; R01 AR074302 United States AR NIAMS NIH HHS |
المشرفين على المادة: | 0 (IFNG protein, human) 0 (IL15 protein, human) 0 (Interleukin-15) 82115-62-6 (Interferon-gamma) |
تواريخ الأحداث: | Date Created: 20200225 Date Completed: 20210401 Latest Revision: 20210903 |
رمز التحديث: | 20221213 |
مُعرف محوري في PubMed: | PMC8223586 |
DOI: | 10.1016/j.jid.2020.01.026 |
PMID: | 32092350 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1523-1747 |
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DOI: | 10.1016/j.jid.2020.01.026 |