Single-cell analysis reveals isotype-specific autoreactive B cell repertoires in Sjögren's syndrome

Microengraving is a novel technology that uses an array of microfabricated subnanoliter wells to isolate and characterize secreted proteins from larger number of single cells. This printing technique permits the capture and characterization of secreted antibodies on glass slides. Here, we profiled t...

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Veröffentlicht in:PloS one 2013-03, Vol.8 (3), p.e58127-e58127
Hauptverfasser: Nguyen, Cuong Q, Ogunniyi, Adebola O, Karabiyik, Afife, Love, J Christopher
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Ogunniyi, Adebola O
Karabiyik, Afife
Love, J Christopher
description Microengraving is a novel technology that uses an array of microfabricated subnanoliter wells to isolate and characterize secreted proteins from larger number of single cells. This printing technique permits the capture and characterization of secreted antibodies on glass slides. Here, we profiled the antigenic repertoires of B cells reacting against salivary gland tissues in Sjögren's syndrome (SjS), an autoimmune disease targeting the exocrine glands. Single-cell suspensions of spleen and cervical lymph node cells prepared from normal C57BL/6 and SjS-susceptible (SjS(s)) C57BL/6.NOD-AecAec2 mice were dispersed into subnanoliter wells (nanowells). Capture slides preincubated with mouse immunoglobulins were used for printing. Detection antibodies included fluorescence conjugated anti-IgG1, salivary gland lysates of C57BL/6 and SjS(s) mice. Results indicate an increase in the frequency of IgG1-secreting cells in the spleen of SjS(s) mice compared to C57BL/6 mice. Cells from the lymph node of SjS(s) mice yield higher instances of IgG1 reactive against salivary gland antigens than cells from the lymph nodes of C57BL/6 mice. These data demonstrate the isotype-specific reactivity of antibodies during the autoimmune process, and further reveals significant differences in the non-autoimmune and autoimmune antibody repertoires. These results support the generation of self-reactive B cell repertoires during the autoimmune process, at the same time, verifying that microengraving of single cells might allow for identification of novel biomarkers in SjS.
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This printing technique permits the capture and characterization of secreted antibodies on glass slides. Here, we profiled the antigenic repertoires of B cells reacting against salivary gland tissues in Sjögren's syndrome (SjS), an autoimmune disease targeting the exocrine glands. Single-cell suspensions of spleen and cervical lymph node cells prepared from normal C57BL/6 and SjS-susceptible (SjS(s)) C57BL/6.NOD-AecAec2 mice were dispersed into subnanoliter wells (nanowells). Capture slides preincubated with mouse immunoglobulins were used for printing. Detection antibodies included fluorescence conjugated anti-IgG1, salivary gland lysates of C57BL/6 and SjS(s) mice. Results indicate an increase in the frequency of IgG1-secreting cells in the spleen of SjS(s) mice compared to C57BL/6 mice. Cells from the lymph node of SjS(s) mice yield higher instances of IgG1 reactive against salivary gland antigens than cells from the lymph nodes of C57BL/6 mice. These data demonstrate the isotype-specific reactivity of antibodies during the autoimmune process, and further reveals significant differences in the non-autoimmune and autoimmune antibody repertoires. 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This printing technique permits the capture and characterization of secreted antibodies on glass slides. Here, we profiled the antigenic repertoires of B cells reacting against salivary gland tissues in Sjögren's syndrome (SjS), an autoimmune disease targeting the exocrine glands. Single-cell suspensions of spleen and cervical lymph node cells prepared from normal C57BL/6 and SjS-susceptible (SjS(s)) C57BL/6.NOD-AecAec2 mice were dispersed into subnanoliter wells (nanowells). Capture slides preincubated with mouse immunoglobulins were used for printing. Detection antibodies included fluorescence conjugated anti-IgG1, salivary gland lysates of C57BL/6 and SjS(s) mice. Results indicate an increase in the frequency of IgG1-secreting cells in the spleen of SjS(s) mice compared to C57BL/6 mice. Cells from the lymph node of SjS(s) mice yield higher instances of IgG1 reactive against salivary gland antigens than cells from the lymph nodes of C57BL/6 mice. 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subjects Animal tissues
Animals
Antibodies
Antibody Specificity - immunology
Antigens
Arthritis
Autoantibodies - immunology
Autoantigens - immunology
Autoimmune diseases
Autoimmunity
B-Lymphocytes - immunology
B-Lymphocytes - metabolism
Bioindicators
Biology
Biomarkers
Cell suspensions
Chemical engineering
Classification
Disease Models, Animal
Exocrine glands
Female
Fluorescence
Immunoglobulin G
Immunoglobulin G - immunology
Immunoglobulin G - metabolism
Immunoglobulin Isotypes - immunology
Immunoglobulin Isotypes - metabolism
Immunoglobulins
Infectious diseases
Lymph nodes
Lymph Nodes - immunology
Lymphatic system
Lymphocytes B
Lysates
Male
Mathematics
Medical research
Medicine
Mice
Pathogenesis
Printing
Proteins
Rheumatism
Rheumatology
Ribonucleoproteins - immunology
Salivary gland
Salivary Glands - immunology
Signal transduction
Single-Cell Analysis - methods
Sjogren's syndrome
Sjogren's Syndrome - immunology
Spleen
Spleen - immunology
Studies
Thyroid gland
Veterinary colleges
Veterinary medicine
title Single-cell analysis reveals isotype-specific autoreactive B cell repertoires in Sjögren's syndrome
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