Supporting Information

Similar documents
The encephalitogenicity of TH17 cells is dependent on IL-1- and IL-23- induced production of the cytokine GM-CSF

Supplemental Figure 1. Signature gene expression in in vitro differentiated Th0, Th1, Th2, Th17 and Treg cells. (A) Naïve CD4 + T cells were cultured

Therapeutic effect of baicalin on experimental autoimmune encephalomyelitis. is mediated by SOCS3 regulatory pathway

IMMUNOTOOLS: EFFECT OF NOTCH-DEFICIENT MACROPHAGES TO AUTOIMMUNE DISEASE WIPAWEE WONGCHANA

Supplemental Materials for. Effects of sphingosine-1-phosphate receptor 1 phosphorylation in response to. FTY720 during neuroinflammation

Supplemental Information. T Cells Enhance Autoimmunity by Restraining Regulatory T Cell Responses via an Interleukin-23-Dependent Mechanism

SUPPLEMENTARY INFORMATION

4. Th1-related gene expression in infected versus mock-infected controls from Fig. 2 with gene annotation.

Intracellular MHC class II molecules promote TLR-triggered innate. immune responses by maintaining Btk activation

Supplementary. presence of the. (c) mrna expression. Error. in naive or

Eosinophils are required. for the maintenance of plasma cells in the bone marrow

Potential Rebalancing of the Immune System by Anti-CD52 Therapy

Supplementary Figure 1. Characterization of basophils after reconstitution of SCID mice

Nature Immunology: doi: /ni.3866

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION

effect on the upregulation of these cell surface markers. The mean peak fluorescence intensity

Cell isolation. Spleen and lymph nodes (axillary, inguinal) were removed from mice

SUPPLEMENTARY INFORMATION

L1 on PyMT tumor cells but Py117 cells are more responsive to IFN-γ. (A) Flow

Supplementary Figure 1: TSLP receptor skin expression in dcssc. A: Healthy control (HC) skin with TSLP receptor expression in brown (10x

Targeting tumour associated macrophages in anti-cancer therapies. Annamaria Gal Seminar Series on Drug Discovery Budapest 5 January 2018

Nature Immunology: doi: /ni Supplementary Figure 1. Production of cytokines and chemokines after vaginal HSV-2 infection.

Thomas HAIDER Journal Club

Integrin CD11b negatively regulates TLR-triggered inflammatory responses by. activating Syk and promoting MyD88 and TRIF degradation via cbl-b

% of live splenocytes. STAT5 deletion. (open shapes) % ROSA + % floxed

SUPPLEMENTARY INFORMATION

ECM1 controls T H 2 cell egress from lymph nodes through re-expression of S1P 1

Supplementary Figure S1. Flow cytometric analysis of the expression of Thy1 in NH cells. Flow cytometric analysis of the expression of T1/ST2 and

Supplementary Information:

CXCL11-dependent induction of FOXP3- negative regulatory T cells suppresses autoimmune encephalomyelitis

Cell-mediated Immunity

Supplementary Fig. 1 p38 MAPK negatively regulates DC differentiation. (a) Western blot analysis of p38 isoform expression in BM cells, immature DCs

Relevant Disclosures

Supplemental Materials

IL-12 family members in experimental colitis. Markus F. Neurath I. Medical Clinic Johannes Gutenberg-University Mainz, Germany

Blocking antibodies and peptides. Rat anti-mouse PD-1 (29F.1A12, rat IgG2a, k), PD-

Reviewers' comments: Reviewer #1 Expert in EAE and IL-17a (Remarks to the Author):

Supplementary Figure 1. mrna expression of chitinase and chitinase-like protein in splenic immune cells. Each splenic immune cell population was

B6/COLODR/SPL/11C/83/LAP/#2.006 B6/COLODR/SPL/11C/86/LAP/#2.016 CD11C B6/COLODR/SPL/11C/80/LAP/#2.011 CD11C

Supporting Information

Supplementary Figure 1 IL-27 IL

B220 CD4 CD8. Figure 1. Confocal Image of Sensitized HLN. Representative image of a sensitized HLN

Supplementary Figure S1. PTPN2 levels are not altered in proliferating CD8+ T cells. Lymph node (LN) CD8+ T cells from C57BL/6 mice were stained with

Lee et al. Molecular Neurodegeneration (2016) 11:54 DOI /s

Supplementary Figure 1.

SUPPLEMENTARY FIGURES

Supplemental Table I.

Supplementary table I. Real-time primers used in the study. The fold change was obtained by

IMO-8400, a novel TLR7, TLR8 and TLR9 antagonist, psoriasis

Supplementary Figure 1 Protease allergens induce IgE and IgG1 production. (a-c)

Regulatory functions of CD8 + CD28 T cells in an autoimmune disease model

SUPPLEMENTARY INFORMATION

PhD thesis. The role of complement in Experimental Autoimmune Encephalomyelitis, the mouse modell of Multiple Sclerosis

Factors Which Predispose to the Onset of Autoimmune Disease. A Senior Honors Thesis

Human Innate Lymphoid Cells: crosstalk with CD4 + regulatory T cells and role in Type 1 Diabetes

Adenovirus engineered human dendritic cell vaccine induces natural killer cell chemotaxis

A novel probiotic mixture exerts a therapeutic effect on experimental autoimmune encephalomyelitis mediated by IL-10 producing regulatory T cells.

Nature Immunology: doi: /ni Supplementary Figure 1. Transcriptional program of the TE and MP CD8 + T cell subsets.

AMDCC Progress Report Duke/UNC/Stanford Unit. Program Director Thomas M. Coffman, MD

Peer review correspondence

SUPPLEMENTARY INFORMATION

STAT5 programs a distinct subset of GM-CSF-producing T helper cells that is essential for autoimmune neuroinflammation

Innate immune regulation of T-helper (Th) cell homeostasis in the intestine

ACTIVATION AND EFFECTOR FUNCTIONS OF CELL-MEDIATED IMMUNITY AND NK CELLS. Choompone Sakonwasun, MD (Hons), FRCPT

Effector T Cells and

activation with anti-cd3/cd28 beads and 3d following transduction. Supplemental Figure 2 shows

Title of file for HTML: Supplementary Information Description: Supplementary Figures and Supplementary Table

well for 2 h at rt. Each dot represents an individual mouse and bar is the mean ±

TITLE: MODULATION OF T CELL TOLERANCE IN A MURINE MODEL FOR IMMUNOTHERAPY OF PROSTATIC ADENOCARCINOMA

SUPPLEMENTARY INFORMATION

Eosinophils! 40! 30! 20! 10! 0! NS!

sequences of a styx mutant reveals a T to A transversion in the donor splice site of intron 5

Effector mechanisms of cell-mediated immunity: Properties of effector, memory and regulatory T cells

Nature Medicine: doi: /nm.3922

Supplemental Information. Gut Microbiota Promotes Hematopoiesis to Control Bacterial Infection. Cell Host & Microbe, Volume 15

Supporting Information

Supplementary Figure 1 Chemokine and chemokine receptor expression during muscle regeneration (a) Analysis of CR3CR1 mrna expression by real time-pcr

MATERIALS AND METHODS. Neutralizing antibodies specific to mouse Dll1, Dll4, J1 and J2 were prepared as described. 1,2 All

Supplementary Information

Supplementary Figure 1. Successful excision of genes from WBM lysates and

Supplementary Figure 1. Normal T lymphocyte populations in Dapk -/- mice. (a) Normal thymic development in Dapk -/- mice. Thymocytes from WT and Dapk

03/24/2017. The intrarenal RAS and blood pressure. The Renin-Angiotensin-Aldosterone System. The Renin-Angiotensin-Aldosterone System

Supplemental Table 1. Primer sequences for transcript analysis

Anti IL-23 therapy inhibits multiple inflammatory pathways and ameliorates autoimmune encephalomyelitis

Nature Immunology: doi: /ni Supplementary Figure 1. Cellularity of leukocytes and their progenitors in naive wild-type and Spp1 / mice.

Supplemental Figure 1

SUPPLEMENTARY FIGURE 1

IL-22 mediates mucosal host defense against gram negative bacterial pneumonia

Supplementary Information

Supplementary Figure 1. ETBF activate Stat3 in B6 and Min mice colons

and follicular helper T cells is Egr2-dependent. (a) Diagrammatic representation of the

Regulatory B cells inhibit EAE initiation in mice while other B cells promote disease progression

Supplementary fig. 1. Crystals induce necroptosis does not involve caspases, TNF receptor or NLRP3. A. Mouse tubular epithelial cells were pretreated

INTRODUCTION. Induction of Monocyte Chemoattractant Protein-1 (MCP-1) Expression by Angiotensin II (AngII) in the Pancreatic Islets and Beta Cells

A new Rag2/Il2rg SCID rat. Enabling cell line xenografts. Accelerating PDX establishment. Humanizing the immune system

Peli1 negatively regulates T-cell activation and prevents autoimmunity

Immunological alterations in mice irradiated with low doses

Endocannabinoid-activated Nlrp3 inflammasome in infiltrating macrophages mediates β- cell loss in type 2 diabetes

IL-17 in health and disease. March 2014 PSO13-C051n

Transcription:

Supporting Information Stegbauer et al. 10.1073/pnas.0903602106 SI Methods Analysis of Plasma Renin Activity (PRA) and ACE Activity. PRA and serum ACE activity levels were determined by RIA (RENCTK, DiaSorin; Bühlmann Laboratories). Renin activity was assayed via AngI production. ACE activity was measured using the ACE-REA kit and defined via inhibition by lisinopril. In short, the synthetic substrate [ 3 H]hippuryl-glycyl-glycine was added and cleaved by angiotensin-converting enzyme to [ 3 H]hippuric acid. Cell Transfer Experiments. In vivo transfer of T cells was performed according to a protocol described in Beyersdorf et al. (1). On day 10 p.i., pan T cells were isolated via MACS (Miltenyi) from the spleens of losartan- or vehicle-treated mice (treatment start on day 3 before immunization). Fifteen mio cells were transferred intraveniously into recipient wild-type mice on day 1 p.i. 1. Beyersdorf N, et al. (2005) Selective targeting of regulatory T cells with CD28 superagonists allow effective therapy of experiental autoimmune encephalomyelitis. J Exp Med 202:445 455. 1of6

Fig. S1. Expression of plasma ACE in autoimmune inflammation of the CNS. Analysis of serum ACE activities in mice suffering from MOG-EAE (day 31 p.i., n 6 15 per group) and matched healthy control mice. While the induction of EAE did not influence ACE levels, there was a significant gender effect, with higher ACE activities in male mice (white and black bars). 2of6

Fig. S2. Expression of RAS components during MOG-EAE (day 31 p.i.) in spinal cord, spleen, T cells, and peritoneal macrophages, as well as in myeloid DCs prepared from bone marrow of naive mice, which were differentiated and matured in vitro for 9 days (d9). Naive control mice (black bars) are compared to EAEdiseased mice (white bars) and EAE-diseased mice with AT1R blockade via losartan (gray bars). Induction of MOG-EAE leads to an (a) up to 3-fold increase in ACE expression in the spinal cord, whereas (b) losartan treatment reduced ACE expression in the spleen compared to vehicle-treated control mice. In macrophages (MP), (c) ACE and (d) ACE2 expression are up-regulated after MOG-EAE induction, without modulating effects of losartan treatment. In differentiated myeloid DCs after 9 days in culture (DC d9), ACE and ACE2 expression is also detectable, with a clear preponderance of ACE. The analysis of T cells from MOG-EAE-diseased mice reveals (e) an AT1aR expression that is not detected in naive controls and (f) an over 10-fold increase in AT1bR expression, while (g) ACE expression and (h) ACE2 expression in T cells are down-regulated after induction of MOG-EAE. AT1R blockade in MOG-EAE leads to a reduced expression of AT1aR and AT1bR in T cells, while levels of ACE and ACE2 are preserved. Data are presented as relative expression with the respective gene expression in EAE control (white bars) set to 1 (n 5 6 per group). n.d. not detectable. 3of6

Fig. S3. (a) Clinical course of MOG-EAE in female C57BL/6 mice after treatment with losartan. AT1R blockade leads to a significantly ameliorated disease course. Data are pooled from 2 experiments (n 12 vs.11 mice per group, P 0.05 on day 14 p.i.). (b) Preventive AT1R blockade with a daily dose of 30 mg/kg body weight losartan (gray curve) leads to a later onset of MOG-EAE and an ameliorated later disease phase. Data are pooled from 2 independent experiments (n 13 vs. 16 mice; P 0.05 on day 16 p.i.). Black bar above graphs in (a) and (b) indicates duration of therapy. (c) In AT1aR knockout (agtr1 / ) mice, there is no compensatory up-regulation of AT1b receptors in spinal cord and spleen. (d)inagtr1 / mice, renin expression is highly up-regulated in (d) spinal cord and (e) spleen as compared to wild-type (agtr1 / ) mice. In wild-type mice, induction of MOG-EAE increases renin expression in (d) spinal cord and (e) spleen. Data are presented as relative expression with the respective gene expression in wild-type mice (black bars) set to 1 (n 4 7 per group). n.d. not detectable. 4of6

Fig. S4. AT1R blockade does not alter the T-cell response in MOG-EAE. (a) Analysis of cytokine production in supernatants from splenocyte primary culture derived from losartan- or vehicle-treated mice. There was no difference in the production of the cytokines IFN-, IL-17, or IL-5, as well as IL-10 and TGF- between losartan- and vehicle-treated mice. Data from a representative experiment with 4 mice per group are shown. (b) Clinical course of MOG-EAE after transfer of T cells from mice treated with losartan from day 3 before immunization ( LOS T cell, gray curve) as compared to vehicle-treated controls ( ctrl T cell, black curve). Preparation of cells on day 10 p.i. and transfer of 15 mio cells into recipient mice on the day before immunization does not alter their course of MOG-EAE (n 8 mice per group). (c) FACS analyses of T cell and natural killer (NK) cell subsets in the spleen on day 10 of MOG-EAE. In comparison to vehicle application (black bars), losartan treatment (white bars) does not significantly change numbers of CD4 or CD8 T cells, NK1.1 CD3 and NK1.1 CD3 cells. 5of6

Fig. S5. AT1R blockade impairs chemokine production in macrophages on the mrna level. Macrophages were prepared on day 16 p.i. of MOG-EAE after in vivo treatment with losartan or vehicle as control, starting 3 days before immunization. In a RT-PCR analysis, there was a significant reduction of CCL2 and a clear trend toward a reduction of CXCL10 after losartan treatment. Data are presented as relative expression with the gene expression in a wild-type mouse set to 1(n 4 vs. 3 mice per group). 6of6