Nature Immunology: doi: /ni Supplementary Figure 1

Similar documents
HHS Public Access Author manuscript Nat Immunol. Author manuscript; available in PMC 2015 March 01.

Nature Immunology: doi: /ni Supplementary Figure 1. Id2 and Id3 define polyclonal T H 1 and T FH cell subsets.

Supplementary Information. Tissue-wide immunity against Leishmania. through collective production of nitric oxide

SUPPLEMENTARY INFORMATION

Supplemental Figure 1

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

BMDCs were generated in vitro from bone marrow cells cultured in 10 % RPMI supplemented

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

Control GST GST-RAP. α2-mg. 170 kda. b-actin. 42 kda LRP-1

Spleen. mlns. E Spleen 4.1. mlns. Spleen. mlns. Mock 17. Mock CD8 HIV-1 CD38 HLA-DR. Ki67. Spleen. Spleen. mlns. Cheng et al. Fig.

Supplemental Table I.

days days and gbt-i.cd Recipient 20

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

a 10 4 Link et al. Supplementary Figure 1 Nature Immunology: doi: /ni.1842 Cells per mouse ( 10 5 ) TRPV2KO anti-gr1 anti-gr anti-f4/80

Akt and mtor pathways differentially regulate the development of natural and inducible. T H 17 cells

<10. IL-1β IL-6 TNF + _ TGF-β + IL-23

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

Supplementary Figure 1. IL-12 serum levels and frequency of subsets in FL patients. (A) IL-12

Phenotype Determines Nanoparticle Uptake by Human

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

Nature Medicine: doi: /nm.3922

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

Supplementary Figure S I: Effects of D4F on body weight and serum lipids in apoe -/- mice.

Supplementary Figure 1

Supplemental Information. CD4 + CD25 + Foxp3 + Regulatory T Cells Promote. Th17 Cells In Vitro and Enhance Host Resistance

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

Supplementary Figures

SUPPLEMENT Supplementary Figure 1: (A) (B)

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

Therapeutic PD L1 and LAG 3 blockade rapidly clears established blood stage Plasmodium infection

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

pro-b large pre-b small pre-b CCCP (µm) Rag1 -/- ;33.C9HCki

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

Supplementary Materials for

Supplemental Materials

Supplementary Figure 1.

LPS LPS P6 - + Supplementary Fig. 1.

Grade of steatosis. group Case No. Supplementary Figure 1:

Type of file: PDF Title of file for HTML: Supplementary Information Description: Supplementary Figures

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

SUPPLEMENTARY INFORMATION. Supp. Fig. 1. Autoimmunity. Tolerance APC APC. T cell. T cell. doi: /nature06253 ICOS ICOS TCR CD28 TCR CD28

SUPPLEMENTARY INFORMATION

Supplementary Figure 1. Efficiency of Mll4 deletion and its effect on T cell populations in the periphery. Nature Immunology: doi: /ni.

Nature Immunology doi: /ni.3268

CD44

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

NK cell flow cytometric assay In vivo DC viability and migration assay

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

Peli1 negatively regulates T-cell activation and prevents autoimmunity

Nature Medicine doi: /nm.3957

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

SUPPLEMENTARY MATERIAL

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

Supplementary Materials for

Lipid (Oil Red O) staining Kit

Tbk1-TKO! DN cells (%)! 15! 10!

ONLINE SUPPLEMENT MATERIAL. CD70 limits atherosclerosis and promotes macrophage function.

Supplementary Figure 1. Double-staining immunofluorescence analysis of invasive colon and breast cancers. Specimens from invasive ductal breast

Supplementary Fig. 1 eif6 +/- mice show a reduction in white adipose tissue, blood lipids and normal glycogen synthesis. The cohort of the original

Supporting Information

Supplemental Information. Aryl Hydrocarbon Receptor Controls. Monocyte Differentiation. into Dendritic Cells versus Macrophages

Nature Immunology: doi: /ni Supplementary Figure 1. RNA-Seq analysis of CD8 + TILs and N-TILs.

SUPPLEMENTARY INFORMATION

genome edited transient transfection, CMV promoter

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 IL-27 IL

Nature Immunology: doi: /ni.3866

Pathologic Stage. Lymph node Stage

Quantitative PPARγ expression affects the balance between tolerance and immunity

Supplementary Figure 1. Antibiotic partially rescues mice from sepsis. (ab) BALB/c mice under CLP were treated with antibiotic or PBS.

Supplementary information to: Mechanism of lipopolysaccharide-induced skin edema formation in the mouse

a surface permeabilized

Supplementary Figures

Hua Tang, Weiping Cao, Sudhir Pai Kasturi, Rajesh Ravindran, Helder I Nakaya, Kousik

Supporting Information

Loss of Calreticulin Uncovers a Critical Role for Calcium in Regulating Cellular Lipid Homeostasis

Fig. S1. REGN1500 reduces plasma levels of cholesterol, TG and NEFA in WT and Ldlr -/- mice. (A) WT

Supplementary Figure 1 IMQ-Induced Mouse Model of Psoriasis. IMQ cream was

Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration Athanasiou et al

Supplementary material. VAMP7 controls T cell activation by regulating recruitment and phosphorylation of vesicular

CD4 + T cells recovered in Rag2 / recipient ( 10 5 ) Heart Lung Pancreas

SUPPLEMENTARY FIGURES

glucose glucose 6-phospho fructose 6-phosphate fructose 1,6-bisphosphate glyceraldehyde 3-phosphate 1,3-bisphosphoglycerate 3-phosphoglycerate

Supplementary Figures

A Slfn2 mutation causes lymphoid and myeloid immunodeficiency due to loss of immune cell quiescence

SUPPLEMENTARY INFORMATION

Suppl. Table 1: CV of pooled lipoprotein fractions analysed by ESI-MS/MS

(A) RT-PCR for components of the Shh/Gli pathway in normal fetus cell (MRC-5) and a

Supplementary Figure 1: Expression of NFAT proteins in Nfat2-deleted B cells (a+b) Protein expression of NFAT2 (a) and NFAT1 (b) in isolated splenic

a. b. c. d. e. f. g. h. i. j. k. l. m. n. o. p.

SUPPLEMENTARY INFORMATION

Fig. S1 A. week 4 week 6

Crucial role for human Toll-like receptor 4 in the development of contact allergy to nickel

SUPPLEMENTARY INFORMATION

Supplementary Figure 1. BMS enhances human T cell activation in vitro in a

Human and mouse T cell regulation mediated by soluble CD52 interaction with Siglec-10. Esther Bandala-Sanchez, Yuxia Zhang, Simone Reinwald,

W/T Itgam -/- F4/80 CD115. F4/80 hi CD115 + F4/80 + CD115 +

Serafino et al. Thymosin α1 activates complement receptor-mediated phagocytosis in human monocyte-derived macrophages. SUPPLEMENTARY FIGURES

Supplementary Figure 1. Immune profiles of untreated and PD-1 blockade resistant EGFR and Kras mouse lung tumors (a) Total lung weight of untreated

Transcription:

Supplementary Figure 1 Fatty acid oxidation is emphasized in 1 macrophages compared with that in macrophages. Gene expression of mitochondrial OXPHOS (Atp5j, Cox4i1, Uqcrc1/2, Ndufs1, Sdhb) and β-oxidation (Acadm, Acox1, Crot, CPT2, Acadl, Crat) pathways in and macrophages. (b) Relative expression in vs. macrophages of key activation indicator genes used for the analysis in a. (c) Expression levels of genes used in this study (GSE5353). Data shown are from two independent RNA-Seq analyses. Nature Immunology: doi:1.138/ni.2956

Supplementary Figure 2 macrophages survive longer than or macrophages do. Cell survival, measured by lack of staining with 7-AAD, in cultured macrophages over time. Tissue culture medium and activation signals (IL-4 for, IFN-γ and LPS for ) were replaced every 2 days. Data points are mean values + SEM for 3 replicate conditions per time point from 1 experiment representative of 2. Nature Immunology: doi:1.138/ni.2956

a b + orlistat Pnpla2 +/+ + PBS Pnpla2 +/+ + IL-4c Pnpla2 -/- + IL-4c 92.5 ± 3.5% 91.7 ± 3.8% 1 2 1 3 1 4 1 5 RELMα c + Lipa shrna 5 nm US + orlistat + CLQ 1 2 1 3 1 4 1 5 1 2 1 3 1 4 1 5 BODIPY 493/53 2 µm d TG(16:,16:,18:1) TG(16:,18:1,18:1) CE16: CE16:1.25.5.8.5.2.15.1.5. + orlistat.4.3.2.1. + orlistat.6.4.2. + orlistat.4.3.2.1. + orlistat TG(18:1,18:,18:) TG(18:1,18:1,18:) CE18:1 CE18:2.15.15.8.25.1.5. + orlistat.1.5. + orlistat.6.4.2. + orlistat.2.15.1.5. + orlistat Nature Immunology: doi:1.138/ni.2956

Supplementary Figure 3 Lack of ATGL does not affect activation in vivo, and lipid droplets accumulate in macrophages when lipolysis is inhibited. (a) activation in peritoneal macrophages from wild-type (Pnpla2 +/+ ) and Pnpla2 -/- mice injected with PBS (wild-type only) or IL-4c was measured by RELMα expression using flow cytometry. Numbers indicate mean ± SEM values for % macrophages positive for RELM in 3 technical replicates per condition. Data are from peritoneal macrophages pooled from 2 mice per group from 1 experiment representative of 3. (b) Representative electron micrographs of macrophages cultured in IL-4 in the presence of orlistat for 24 h ( + orlistat) and of Lipa shrna-transduced macrophages cultured in IL-4 for 24 h ( + Lipa shrna); These images from 1 experiment representative of 2. c) Neutral lipid accumulation in macrophages cultured in complete medium in the absence or presence of orlistat or chloroquine (CLQ). Neutral lipids were detected by BODIPY staining followed by flow cytometry. Fluorescence staining was compared to unstained cells (US), cells, and to cells cultured without orlistat or CLQ. Data are from 1 experiment representative of 2. (d) Mass spectrometric quantitation of different triacylglycerol (TG) and cholesterol ester (CE) species in.,, and orlistat treated macrophages. Ratios reflect fatty acid chain length to double bonds for the species detected in TGs, or for CEs. In d, data are mean ± SEM values from 2 replicate samples from one experiment. Numbers above graph bars show actual mean values per condition. Nature Immunology: doi:1.138/ni.2956

a US Cd36 + + Cd36 BODIPY-Palmitate (gmfi) 6 1 3 5 1 3 4 1 3 3 1 3 2 1 3 1 1 3 Cd36 + + Cd36 b US + SSO 1 2 1 3 1 4 1 5 BODIPY-Palmitate 1 2 1 3 1 4 1 5 BODIPY-LDL c OCR (pmol/min) 2 15 1 5 *** OCR/ECAR (pmol/mph) 8 *** 6 4 2 + SSO SRC (%) 15 1 5 ** + SSO d OCR (pmol/min) 12 9 6 3 OCR/ECAR (pmol/mph) 6 5 4 3 2 1 + SSO e f CD31 PD-L2 + SSO 1 5 1.5 ±.4 29.4 ± 5. 5.3 ±.1 1 4 1 3 1 2 1 2 1 3 1 4 1 5 CD26 1 5 1.1 ±.1 45.7 ± 3.6 19.9 ± 4.4 1 4 1 3 1 2 1 2 1 3 1 4 1 5 RELMα 1 2 1 3 1 4 1 5 inos + SSO 62.8 ± 11.7% 64.4 ± 8.4% Supplementary Figure 4 CD36 is not required for increased palmitate uptake by macrophages but is important for LDL uptake and activation. (a) BODIPY-palmitate uptake by WT and Cd36 -/- and macrophages, as measured by flow cytometry. (b-g) The effect of the CD36 inhibitor sulfo-n-succinimidyl oleate (SSO) on (b) the uptake of LDL by macrophages, (c) basal OCR, the ratio of basal OCR to basal ECAR, and SRC in macrophages, (d) basal OCR and the ratio of basal OCR to basal ECAR in macrophages, (e) CD26 and CD31 expression and PD-L2 and RELMα expression by macrophages, (f) inos expression by macrophages. In b-g macrophages were pre-treated with SSO for 3 minutes prior to the addition of polarizing stimuli, and data were collected 24 h later. Data in b-g from macrophages are shown for comparison. Data in the histograms in a and b are from 1 experiment representative of 2. Data in the bar graph in a are means ± SEM of data from 2 independent experiments. Data in c and d are means ± SEM of 3 technical replicates from one experiment representative of 3. Numbers in e refer to the percentages of macrophages that fall within the indicated gates. Plots are from one representative experiment, numbers are means ± SEM of data from 3 independent experiments. In f, histograms showing expression of inos are from one experiment representative of 2, numbers are means ± SEM from 2 independent experiments of % of cells expressing inos. P values are from Student s t-test (*P <.1; **P < Nature Immunology: doi:1.138/ni.2956

.1). Nature Immunology: doi:1.138/ni.2956

a PD-L2 + Serum + 5-L/V + 5-L/V Serum 1 5 1.4 ±.1 3.9 ± 1.4 27.9 ± 1.4 17.4 ± 3.1 14.3 ±.9 1 4 1 3 1 2 1 2 1 3 1 4 1 5 RELMα b 1.2 ±.2 + orlistat + TOFA + orlistat + TOFA 37.3 ± 7. 18.7 ± 5.3 21.8 ± 9.4 13.3 ± 6.2 + Serum Serum PD-L2 1 5 1 4 1 3 1.3 ±.3 16.1 ± 8.5 7.1 ± 2.1.1 ±.3.3 ±.1 1 2 1 2 1 3 1 4 1 5 RELMα Supplementary Figure 5 activation can occur in serum-free conditions but is increased by the addition of serum or LDL and VLDL. (a) Macrophages were cultured with IL-4 () for 24 h in medium containing (+Serum) or lacking serum (-Serum), or in serum free medium with added 5 or 5 μg/ml of LDL/VLDL (5-L/V or 5-L/V). PD-L2 and RELMα expression were measured by flow cytometry, (b) Macrophages were cultured with IL-4 for 24 h in the absence () or presence of inhibitors of lipolysis (orlistat) or fatty acid synthesis (TOFA), in medium containing (+Serum) or lacking (-Serum) serum. In both a and b, cells destined to be tested in serum-free medium were pre-cultured under these conditions for 24 h prior to the addition of IL-4. Numbers refer to the percentages of macrophages that fall within the indicated gates. Plots are from one experiment representative of 2, numbers are means ± SEM of data from 2 independent experiments. Nature Immunology: doi:1.138/ni.2956

a b total cells (x1 7 ) 12 1 8 6 4 NS NS Naive 1 Hp 1 Hp + orlistat 2 Hp 2 Hp + orlistat hucd2 1 5 1 4 1 3 1 2 Naïve.3 1 Hp 12 1 Hp + orlistat 1 2 1 2 1 3 1 4 1 5 GFP 2 Hp 2 Hp + orlistat 1 5 1 4 1 3 1 1 hucd2 1 2 1 2 1 3 1 4 1 5 GFP Supplementary Figure 6 Inhibition of lipolysis does not prevent IL-4 production by T H 2 cells during H. polygyrus infection. 4get/KN2 IL-4 reporter mice were infected with H. polygyrus and treated with the anti-helminthic pyrantel pamoate prior to receiving a secondary infection (2ºHp). At the time of secondary infection, additional groups of mice were infected for the first time to provide primary H. polygyrus infection controls (1ºHp). Infected mice were treated with Orlistat, or remained untreated, as indicated. At day 9 post infection, mice were sacrificed and mesenteric lymph nodes were removed. (a) Cellularity of mesenteric lymph nodes in naïve 4get/KN2 mice and in infected mice mice treated variously as shown. (b) IL-4 production, as measured by flow cytometric analysis of expression of hucd2 and GFP immediately ex vivo, in gated CD4 + T cells from mesenteric lymph nodes of 4get/KN2 mice under the conditions shown (see Fig. 7 legend for more details). In these plots, GPF expression reflects transcription of the Il4 gene, and hucd2 expression reflects IL-4 protein production. Data in a represent mean values ± SEM from 3 or more individually assessed mice from 1 experiment representative of 2. Data in b are from lymph nodes pooled from 3 or more mice per group from 1 experiment representative of 2. Numbers in b represent percentages of CD4 + T cells falling within indicated gates. NS = not significant according to Student s t-test. Nature Immunology: doi:1.138/ni.2956