دورية أكاديمية

Multiple receptors converge on H2-Q10 to regulate NK and γδT-cell development.

التفاصيل البيبلوغرافية
العنوان: Multiple receptors converge on H2-Q10 to regulate NK and γδT-cell development.
المؤلفون: Goodall KJ; Department of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia., Nguyen A; Department of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia., Matsumoto A; Baker Heart and Diabetes Institute, Melbourne, VIC, Australia., McMullen JR; Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.; Department of Medicine, Monash University, Clayton, VIC, Australia.; Department of Physiology, Monash University, Clayton, VIC, Australia., Eckle SB; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia., Bertolino P; Liver Immunology program Centenary Institute, AW Morrow Gastroenterology and Liver Centre and Royal Prince Alfred Hospital, University of Sydney, Sydney, NSW, Australia., Sullivan LC; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia., Andrews DM; Department of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.
المصدر: Immunology and cell biology [Immunol Cell Biol] 2019 Mar; Vol. 97 (3), pp. 326-339. Date of Electronic Publication: 2019 Jan 13.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8706300 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1440-1711 (Electronic) Linking ISSN: 08189641 NLM ISO Abbreviation: Immunol Cell Biol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2018- : [Hoboken, NJ] : Wiley
Original Publication: [Adelaide, South Australia] : University of Adelaide, [c1987-
مواضيع طبية MeSH: H-2 Antigens/*immunology , Killer Cells, Natural/*immunology , Killer Cells, Natural/*metabolism , Receptors, Antigen, T-Cell, gamma-delta/*metabolism , Receptors, Immunologic/*metabolism , T-Lymphocyte Subsets/*immunology , T-Lymphocyte Subsets/*metabolism, Animals ; Biomarkers ; CD8-Positive T-Lymphocytes/cytology ; CD8-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/metabolism ; Cell Differentiation/genetics ; Cell Differentiation/immunology ; H-2 Antigens/genetics ; H-2 Antigens/metabolism ; Immunomodulation/genetics ; Immunophenotyping ; Killer Cells, Natural/cytology ; Ligands ; Liver/immunology ; Liver/metabolism ; Mice ; Protein Binding ; T-Lymphocyte Subsets/cytology
مستخلص: Class Ib major histocompatibility complex (MHC) is an extended family of molecules, which demonstrate tissue-specific expression and presentation of monomorphic antigens. These characteristics tend to imbue class Ib MHC with unique functions. H2-Q10 is potentially one such molecule that is overexpressed in the liver but its immunological function is not known. We have previously shown that H2-Q10 is a ligand for the natural killer cell receptor Ly49C and now, using H2-Q10-deficient mice, we demonstrate that H2-Q10 can also stabilize the expression of Qa-1b. In the absence of H2-Q10, the development and maturation of conventional hepatic natural killer cells is disrupted. We also provide evidence that H2-Q10 is a new high affinity ligand for CD8αα and controls the development of liver-resident CD8αα γδT cells. These data demonstrate that H2-Q10 has multiple roles in the development of immune subsets and identify an overlap of recognition within the class Ib MHC that is likely to be relevant to the regulation of immunity.
(© 2018 Australasian Society for Immunology Inc.)
فهرسة مساهمة: Keywords: CD8αα; natural killer cells; non-classical MHC; γδT cells
المشرفين على المادة: 0 (Biomarkers)
0 (H-2 Antigens)
0 (Ligands)
0 (Receptors, Antigen, T-Cell, gamma-delta)
0 (Receptors, Immunologic)
تواريخ الأحداث: Date Created: 20181212 Date Completed: 20200116 Latest Revision: 20200116
رمز التحديث: 20221213
DOI: 10.1111/imcb.12222
PMID: 30537346
قاعدة البيانات: MEDLINE
الوصف
تدمد:1440-1711
DOI:10.1111/imcb.12222