Journal: Cell Reports

Article Title: Aryl Hydrocarbon Receptor Contributes to the Transcriptional Program of IL-10-Producing Regulatory B Cells

doi: 10.1016/j.celrep.2019.10.018

Figure Lengend Snippet:

Article Snippet: Negative CD43- Isolation Kit , Miltenyi Biotec , Cat# 130-049-801.

Techniques: Western Blot, Recombinant, Methylation, Adjuvant, Enzyme-linked Immunosorbent Assay, Isolation, cDNA Synthesis, SYBR Green Assay, DNA Library Preparation, Purification, Bicinchoninic Acid Protein Assay, Microarray, Ex Vivo, Generated, Software, Red Blood Cell Lysis, Staining, Lysis

Journal: bioRxiv

Article Title: Altered X-chromosome inactivation predisposes to autoimmune manifestations in mice

doi: 10.1101/2023.04.20.537662

Figure Lengend Snippet: a. Spleen weight of wild-type (WT) and Ftx KO females at 3-months, 1-year and 2-years of age. Median values are shown. ( t-test , * p -values < 0.05). Underneath, representative images of WT and Ftx KO spleens from 3-month, 1-year and 2-year-old females. b. Representative images of hematoxylin-eosin staining on sections of spleens from 1-year-old WT and Ftx KO females. Scale bar; 100 μm. c. Representative flow cytometry analysis of splenic myeloid dendritic cells (m-DC) in WT and Ftx KO 1-year-old females. On the right, percentages of splenic m-DC (CD11b + CD11c + ) and splenic plasmacytoid dendritic cells (p-DC) (CD11c + B220 + SiglecH + ) in leucocytes. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05). d. Representative flow cytometry analysis of spontaneously activated B cells (B220 + CD69 + ) (upper panels) or of spontaneously activated T cells (CD4 + CD69 + ) (lower panels) in spleen from 1-year-old WT and Ftx KO females. Percentages in leucocytes are shown on the graphs beneath. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05). e. IgG2a natural antibody levels in sera of 1-year- and 2-year-old WT or Ftx KO females measured by ELISA. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05). f. Representative flow cytometry analysis of (B220 + CD138 + ) plasma cells in the spleen of 1-year-old WT and Ftx KO females. Percentages in leucocytes are shown on the graphs beneath. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05). g. Representative flow cytometry analysis of (CD19 + B220 lo CD5 + ) natural antibody producing B1a in the peritoneal cavity (PerC) of 1-year-old WT and Ftx KO females. Percentages in leucocytes are shown on the graphs beneath. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05). h. Cytokines levels in the blood analysed with CBA assays on sera from 3-month-, 1-year-, or 2-year-old WT and Ftx KO females. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05). i. Representative flow cytometry analysis of monocyte populations including non-classical (CD11b hi CD43 lo Ly6C + ) scavenger monocytes in the spleen of 1-year-old WT and Ftx KO females. Percentages in leucocytes are shown on the graphs beneath. Each triangle represents a mouse. Median values are shown. ( t-test , * p -values < 0.05).

Article Snippet: Bone marrow, spleen, blood and peritoneal cavity cells were stained using the following antibodies: CD3 PerCP-Vio770 (130-119-656, Miltenyi Biotec), CD4-APC (130-123-207, Miltenyi Biotec), CD5-APC-Vio770 (130-120-165, Miltenyi Biotec), CD8-FITC (130-118-468, Miltenyi Biotec), CD11b APC (553312, BD Pharmingen), CD11c PE-Vio770 (130-110-840, Miltenyi Biotec), CD19-FITC (557398, BD Pharmingen), CD21-APC-Vio770 (130-111-733, Miltenyi Biotec), CD23-PE-Vio770 (130-118-764, Miltenyi Biotec), CD38-PE (130-123-571, Miltenyi Biotec), CD43-PE (130-112-887, Miltenyi Biotec), CD69-PE (130-115-575, Miltenyi Biotec), CD138 PE-Vio615 (130-108-989, Miltenyi Biotec), F4/80 FITC (130-117-509, Miltenyi Biotec), Ter119 PE (130-112-909, Miltenyi Biotec), SiglecH APC-Vio770 (130-112-299, Miltenyi Biotec), B220-APC (130-110-847, Miltenyi Biotec), B220 VioBlue (130-110-851, Miltenyi Biotec), IgM-VioBlue (130-116-318, Miltenyi Biotec), IgD-PE (130-111-496, Miltenyi Biotec), GL7-PE-Cy7 (144619, BioLegend), Ly6C-FITC (130-111-915, Miltenyi Biotec) following recommendations of the manufacturers.

Techniques: Staining, Flow Cytometry, Enzyme-linked Immunosorbent Assay, Clinical Proteomics

Journal: Science Advances

Article Title: AFF3, a susceptibility factor for autoimmune diseases, is a molecular facilitator of immunoglobulin class switch recombination

doi: 10.1126/sciadv.abq0008

Figure Lengend Snippet: ( A ) Serum antibodies from Aff3 flox/flox Cd4cre and Cd19cre mice were measured by ELISA ( n = 5 in each group). ( B ) Flow cytometry analysis of class switching to IgG1. CD43 − B cells were harvested from Aff3 +/− (purple) or Aff3 −/− (red) mice and cultured with LPS and IL-4 (10 μg/ml). After 4 days, the cells were analyzed by flow cytometry. The panels show the IgG1 and IgG3 expression profiles and the statistical analysis ( n = 4 in each group). ( C ) Flow cytometry analysis of class switching to IgG2c. CD43 − B cells were cultured with LPS and IFN-γ (10 μg/ml). The panels show the IgG2c expression profiles and the statistical analysis ( n = 3 in each group). ( D ) Overexpression of the AFF3 compensated for the Aff3 −/− phenotype. CD43 − B cells were harvested from Aff3 −/− mice and cultured with LPS and IL-4. The cDNAs of Aff3 , Aff1 , and Aff4 were transduced with a retroviral vector carrying the green fluorescent protein (GFP) marker. The panel shows the percentage of IgG1 + cells in GFP + CD19 + cells ( n = 3 in each group). EV, empty vector. The data are shown as means ± SEM. * P < 0.05, *** P < 0.005, and **** P < 0.001. The P values were calculated using unpaired t test with Welch’s correction in (A to C) and via one-way ANOVA with Dunnett’s multiple comparisons test in (D). The data shown in this figure are representative of at least two experiments.

Article Snippet: Naïve B cells were purified by negative selection using a biotin-conjugated anti-CD43 antibody (Miltenyi Biotec, 130-101-954) and anti-biotin magnetic beads (Miltenyi Biotec, 130-090-485) according to the manufacturer’s protocol.

Techniques: Enzyme-linked Immunosorbent Assay, Flow Cytometry, Cell Culture, Expressing, Over Expression, Transduction, Retroviral, Plasmid Preparation, Marker

Journal: Science Advances

Article Title: AFF3, a susceptibility factor for autoimmune diseases, is a molecular facilitator of immunoglobulin class switch recombination

doi: 10.1126/sciadv.abq0008

Figure Lengend Snippet: ( A ) CD43 − B cells were stained with CFSE and cultured. The cells were analyzed by flow cytometry. ( B ) Transcriptome analysis of Aff3 -deficient B cells. CD43 − B cells were cultured with LPS and IL-4. After 3 days of culture, total RNA was prepared and analyzed on a cDNA microarray. ( C ) Quantitative reverse transcription polymerase chain reaction (qRT-PCR) and Western blotting analyses of Aicda ( n = 3 in each group for RT-PCR). CD43 − B cells were cultured with LPS (10 μg/ml) and IL-4 (10 ng/ml). Western blotting was performed with anti-AID antibody, and the membrane was reprobed with anti–extracellular signal–regulated kinase 1/2 (ERK1/2) antibody to assess the loading amounts. nt, nucleotide. ( D ) AFF3 binds to switch regions. CD43 − B cells were cultured with LPS (10 μg/ml) and IL-4 (10 ng/ml) for 3 days. Empty (purple) or 3xFLAG-tagged cDNA of the C-terminal half of Aff3 (red) was transduced. The efficiency of transduction was estimated on the basis of the expression of enhanced GFP (EGFP), which was coexpressed with AFF3 by IRES (internal ribosomal entry site) insertion. Then, the cells were analyzed by ChIP with an anti-FLAG antibody. The amount of DNA precipitated was measured by real-time PCR ( n = 3 in each group), with primers specific to the switch regions or the Acta (encoding α-actin) gene serving as a negative control. Sμ-SR indicates the switch region of IgM (table S4) . Sγ1-c and Sγ1-d indicate the switch region of IgG1 (fig. S7 and table S4). In (C and D), the data are shown as means ± SEM. **** P < 0.001. The P values were calculated using unpaired t tests with Welch’s correction. The data shown in this figure are representative of at least two experiments except for those in (B). The primers used in the experiments are listed in table S4.

Article Snippet: Naïve B cells were purified by negative selection using a biotin-conjugated anti-CD43 antibody (Miltenyi Biotec, 130-101-954) and anti-biotin magnetic beads (Miltenyi Biotec, 130-090-485) according to the manufacturer’s protocol.

Techniques: Staining, Cell Culture, Flow Cytometry, Microarray, Reverse Transcription, Polymerase Chain Reaction, Quantitative RT-PCR, Western Blot, Reverse Transcription Polymerase Chain Reaction, Membrane, Transduction, Expressing, Real-time Polymerase Chain Reaction, Negative Control

Journal: Science Advances

Article Title: AFF3, a susceptibility factor for autoimmune diseases, is a molecular facilitator of immunoglobulin class switch recombination

doi: 10.1126/sciadv.abq0008

Figure Lengend Snippet: ( A ) qRT-PCR was used to analyze the germline and postswitch transcript levels of IgG1 ( n = 3 in each group). Aff3 +/− (purple) or Aff3 −/− (red) CD43 − B cells were cultured with LPS (10 μg/ml) and the indicated amount of IL-4. After 3 days of culture, total RNA was extracted from the cells and analyzed. ( B ) Semiquantitative PCR was performed to analyze CSR. CD43 B cells were cultured as described in (A), and genomic DNA was extracted. PCR of the IgM and IgG1 switch regions in combination was performed with the indicated primers. The genomic DNA was serially diluted and used as the template for PCR. Primers for CD19 were used as an internal control. ( C ) Genomic DNA was prepared as described in (B). Fragments of IgM-IgG1 chimeric switch regions were amplified by nested PCR. The fragments were sequenced, and the mutation rates per nucleotide were plotted ( n = 3 in each group). The detailed data are shown in table S1. In (A and C), the data are shown as means ± SEM. * P < 0.05 and *** P < 0.005. The P values were calculated using unpaired t tests with Welch’s correction. The data in (A and B) are representative of at least two experiments. The primers used are listed in table S4.

Article Snippet: Naïve B cells were purified by negative selection using a biotin-conjugated anti-CD43 antibody (Miltenyi Biotec, 130-101-954) and anti-biotin magnetic beads (Miltenyi Biotec, 130-090-485) according to the manufacturer’s protocol.

Techniques: Quantitative RT-PCR, Cell Culture, Control, Amplification, Nested PCR, Mutagenesis