دورية أكاديمية
Natural killer-like B cells are a distinct but infrequent innate immune cell subset modulated by SIV infection of rhesus macaques.
العنوان: | Natural killer-like B cells are a distinct but infrequent innate immune cell subset modulated by SIV infection of rhesus macaques. |
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المؤلفون: | Manickam C; Division of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University, Durham, North Carolina, United States of America.; Department of Surgery, Duke University, Durham, North Carolina, United States of America., Upadhyay AA; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, United States of America.; Division of Microbiology and Immunology, Emory National Primate Research Center, Atlanta, Georgia, United States of America., Woolley G; Division of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University, Durham, North Carolina, United States of America.; Department of Surgery, Duke University, Durham, North Carolina, United States of America., Kroll KW; Division of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University, Durham, North Carolina, United States of America.; Department of Surgery, Duke University, Durham, North Carolina, United States of America., Terry K; Division of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University, Durham, North Carolina, United States of America.; Department of Surgery, Duke University, Durham, North Carolina, United States of America., Broedlow CA; Division of Surgical Outcomes and Precision Medicine Research, Department of Surgery, University of Minnesota, Minneapolis, Minnesota, United States of America., Klatt NR; Division of Surgical Outcomes and Precision Medicine Research, Department of Surgery, University of Minnesota, Minneapolis, Minnesota, United States of America., Bosinger SE; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, United States of America.; Division of Microbiology and Immunology, Emory National Primate Research Center, Atlanta, Georgia, United States of America., Reeves RK; Division of Innate and Comparative Immunology, Center for Human Systems Immunology, Duke University, Durham, North Carolina, United States of America.; Department of Surgery, Duke University, Durham, North Carolina, United States of America. |
المصدر: | PLoS pathogens [PLoS Pathog] 2024 May 13; Vol. 20 (5), pp. e1012223. Date of Electronic Publication: 2024 May 13 (Print Publication: 2024). |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101238921 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7374 (Electronic) Linking ISSN: 15537366 NLM ISO Abbreviation: PLoS Pathog Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: San Francisco, CA : Public Library of Science, c2005- |
مواضيع طبية MeSH: | Macaca mulatta* , Simian Acquired Immunodeficiency Syndrome*/immunology , Simian Acquired Immunodeficiency Syndrome*/virology , Simian Immunodeficiency Virus*/immunology , Immunity, Innate* , Killer Cells, Natural*/immunology, Animals ; B-Lymphocytes/immunology |
مستخلص: | Natural killer-like B (NKB) cells are unique innate immune cells expressing both natural killer (NK) and B cell receptors. As first responders to infection, they secrete IL-18 to induce a critical cascade of innate and adaptive immune cell infiltration and activation. However, limited research exists on the role of NKB cells in homeostasis and infection, largely due to incomplete and erroneous evaluations. To fill this knowledge gap, we investigated the expression of signaling and trafficking proteins, and the in situ localization and transcriptome of naïve NKB cells compared to conventionally-defined NK and B cells, as well as modulations of these cells in SIV infection. Intracellular signaling proteins and trafficking markers were expressed differentially on naïve NKB cells, with high expression of CD62L and Syk, and low expression of CD69, α4β7, FcRg, Zap70, and CD3z, findings which were more similar to B cells than NK cells. CD20+NKG2a/c+ NKB cells were identified in spleen, mesenteric lymph nodes (MLN), colon, jejunum, and liver of naïve rhesus macaques (RM) via tissue imaging, with NKB cell counts concentrated in spleen and MLN. For the first time, single cell RNA sequencing (scRNAseq), including B cell receptor (BCR) sequencing, of sorted NKB cells confirmed that NKB cells are unique. Transcriptomic analysis of naïve splenic NKB cells by scRNAseq showed that NKB cells undergo somatic hypermutation and express Ig receptors, similar to B cells. While only 15% of sorted NKB cells showed transcript expression of both KLRC1 (NKG2A) and MS4A1 (CD20) genes, only 5% of cells expressed KLRC1, MS4A1, and IgH/IgL transcripts. We observed expanded NKB frequencies in RM gut and buccal mucosa as early as 14 and 35 days post-SIV infection, respectively. Further, mucosal and peripheral NKB cells were associated with colorectal cytokine milieu and oral microbiome changes, respectively. Our studies indicate that NKB cells gated on CD3-CD14-CD20+NKG2A/C+ cells were inclusive of transcriptomically conventional B and NK cells in addition to true NKB cells, confounding accurate phenotyping and frequency recordings that could only be resolved using genomic techniques. Although NKB cells were clearly elevated during SIV infection and associated with inflammatory changes during infection, further interrogation is necessary to acurately identify the true phenotype and significance of NKB cells in infection and inflammation. Competing Interests: The authors have declared that no competing interests exist. (Copyright: © 2024 Manickam et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.) |
References: | Mucosal Immunol. 2016 May;9(3):677-88. (PMID: 26376368) Heliyon. 2023 Feb 03;9(2):e13475. (PMID: 36820037) Cell Mol Immunol. 2013 Mar;10(2):113-21. (PMID: 23396472) Int J Mol Sci. 2023 Mar 09;24(6):. (PMID: 36982305) Nat Methods. 2012 Jul;9(7):671-5. (PMID: 22930834) Microbiome. 2020 Nov 6;8(1):154. (PMID: 33158452) Nat Med. 2006 Dec;12(12):1365-71. (PMID: 17115046) Immunity. 2016 Jul 19;45(1):8-10. (PMID: 27438761) Chin Med J (Engl). 2021 Oct 20;134(23):2788-2798. (PMID: 34670249) Genome Med. 2018 Mar 20;10(1):20. (PMID: 29558968) AIDS. 2018 Jul 31;32(12):1571-1578. (PMID: 29734222) Front Immunol. 2017 Oct 27;8:1407. (PMID: 29163486) Front Immunol. 2018 May 16;9:1064. (PMID: 29868023) J Virol. 2022 Apr 13;96(7):e0023522. (PMID: 35311549) Immunity. 2017 Aug 15;47(2):201-202. (PMID: 28813648) Immunol Res. 2016 Dec;64(5-6):1118-1132. (PMID: 27590022) Int Immunopharmacol. 2021 Dec;101(Pt B):107598. (PMID: 34233864) J Leukoc Biol. 2019 May;105(5):843-856. (PMID: 30457676) Sci Rep. 2020 Sep 21;10(1):15363. (PMID: 32958790) Am J Pathol. 2006 Mar;168(3):835-46. (PMID: 16507899) Cold Spring Harb Perspect Med. 2012 Jul;2(7):a007070. (PMID: 22762020) Nat Rev Immunol. 2013 Feb;13(2):118-32. (PMID: 23348416) Springer Semin Immunopathol. 2005 Mar;26(4):377-83. (PMID: 15645296) Growth Factors. 2005 Mar;23(1):33-41. (PMID: 16019425) Immunol Rev. 2009 Jan;227(1):234-47. (PMID: 19120488) Nat Biotechnol. 2018 Jun;36(5):411-420. (PMID: 29608179) Front Immunol. 2021 Feb 18;12:641562. (PMID: 33679805) Sci Immunol. 2019 Mar 1;4(33):. (PMID: 30824527) Cell Death Discov. 2022 May 6;8(1):251. (PMID: 35523778) Sci Rep. 2021 Jul 15;11(1):14507. (PMID: 34267278) Front Immunol. 2022 Aug 11;13:919973. (PMID: 36032110) Int Immunopharmacol. 2019 May;70:477-485. (PMID: 30870678) F1000Res. 2019 May 3;8:616. (PMID: 31448103) Clin Rev Allergy Immunol. 2020 Feb;58(1):92-106. (PMID: 31183788) Immunity. 2016 Jul 19;45(1):131-44. (PMID: 27421702) Clin Oral Investig. 2022 Feb;26(2):2187-2195. (PMID: 34601633) Oral Surg Oral Med Oral Pathol. 1992 Feb;73(2):145-50. (PMID: 1532235) Bioinformatics. 2013 Jan 1;29(1):15-21. (PMID: 23104886) mSphere. 2020 Feb 5;5(1):. (PMID: 32024706) Front Microbiol. 2019 May 22;10:1104. (PMID: 31191468) Immunity. 2017 Aug 15;47(2):199-200. (PMID: 28813647) Nat Immunol. 2015 Jun;16(6):554-62. (PMID: 25988887) FEBS Lett. 1992 Jul 27;307(1):97-101. (PMID: 1639201) J Interferon Cytokine Res. 2009 Jun;29(6):313-26. (PMID: 19441883) Curr Opin Immunol. 2018 Feb;50:9-13. (PMID: 29078198) Mucosal Immunol. 2008 Jan;1(1):23-30. (PMID: 19079157) Nucleic Acids Res. 2013 Jul;41(Web Server issue):W34-40. (PMID: 23671333) Biol Direct. 2014 Oct 14;9(1):20. (PMID: 25319552) Int J Syst Evol Microbiol. 2013 Apr;63(Pt 4):1214-1218. (PMID: 22753527) Pediatr Nephrol. 1999 Sep;13(7):586-93. (PMID: 10460507) Front Immunol. 2022 Nov 03;13:972435. (PMID: 36405684) Genome Biol. 2015 Dec 10;16:278. (PMID: 26653891) Immunity. 2021 Feb 9;54(2):355-366.e4. (PMID: 33484642) Immunol Rev. 2013 Jul;254(1):10-33. (PMID: 23772612) Cell. 2019 May 16;177(5):1153-1171.e28. (PMID: 31080066) |
معلومات مُعتمدة: | P51 OD011132 United States OD NIH HHS; R01 AI161010 United States AI NIAID NIH HHS; R01 AI143457 United States AI NIAID NIH HHS; P01 AI162242 United States AI NIAID NIH HHS; R21 AI145678 United States AI NIAID NIH HHS; S10 OD026799 United States OD NIH HHS |
تواريخ الأحداث: | Date Created: 20240513 Date Completed: 20240523 Latest Revision: 20240525 |
رمز التحديث: | 20240525 |
مُعرف محوري في PubMed: | PMC11115201 |
DOI: | 10.1371/journal.ppat.1012223 |
PMID: | 38739675 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1553-7374 |
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DOI: | 10.1371/journal.ppat.1012223 |