Journal: Frontiers in Immunology

Article Title: Targeting Nuclear LSD1 to Reprogram Cancer Cells and Reinvigorate Exhausted T Cells via a Novel LSD1-EOMES Switch

doi: 10.3389/fimmu.2020.01228

Figure Lengend Snippet: LSD1 inhibition re-invigorates CD8 + T cell subsets in mouse models. (A) Schematic of the metastatic breast cancer mouse model. Tumor samples from 3 individual animals/group were collected on day 15, RNA was extracted, and gene expression measured using the nanostring pancancer immune profiling panel. (B) Bar chart of -log10 transformed p -values across cell types by nCounter advanced analysis. Characteristic genes of various immune cell populations measure each population's abundance within the tumor sample. Immune pathway scores against treatment conditions defined using the first principal component of each geneset's data and each sample's gene expression profile condensed into a small set of pathway scores including innate, adaptive, humoral, and inflammation pathways. Total number of induced and inhibited genes for immune-related pathways analyzed by nanostring. Statistically significantly differentially expressed genes are defined by 2-fold linear changes with p < 0.05 compared to control samples. Yellow bar plot represents phenelzine, red bar plot represents anti-PD-1. (C) 4T1 tumor-bearing mice were treated with vehicle control, phenelzine (40 mg/kg), or EPI-111 (20 mg/kg). Fifteen days post-treatment, the primary tumors were measured and harvested and collected for nanostring analysis. NanoString global significance scores for RNA isolated from whole tumors. Heatmap displaying each sample's directed global significance scores. Directed global significance statistics measure the extent to which a geneset's genes are up- or down-regulated with the variable. Red denotes genesets whose genes exhibit extensive over-expression with the covariate, blue denotes genesets with extensive under-expression. NanoString analysis was performed in triplicate. (D) Jurkat T cells were treated with phenelzine or GSK for 10 h followed by inhibition withdrawal and resting for different time points. After resting for 24 h, cells were re-inhibited with phenelzine or GSK followed by repeat inhibition (PMA/CaI for 2 h), withdrawal, and resting. IFN-γ expression levels were measured by RT-PCR and normalized to GAPDH. Data represent the fold changes in expression of stimulated samples compared to control non-stimulated samples. Expression values are the average of the RT-PCR (technical) replicates, and error bars indicate min-max. (E) T cells isolated from 4T1 tumors were stimulated with PMA/ionomycin for 4 h in the presence of brefeldin A, stained for IFN-γ, and analyzed by flow cytometry (* p < 0.05, n = 3). Data overlies total CD8 + T cell infiltration into the primary tumor ( n = 5 mice per group). Treatment groups are control, abraxane (30 mg/kg), anti-PD1 (10 mg/kg), phenelzine (40 mg/kg), anti-PD1 and phenelzine, or triple therapy. (F) 4T1 breast cancer treatment regimen. Treatment groups from left to right: Control, Abraxane (30 mg/kg), phenelzine (40 mg/kg), EPI-111 (1 mg/kg), EPI-111 (4 mg/kg), and EPI-111 (20 mg/kg), with 5 mice per group. (G) Cells were taken for FACS analysis from primary tumors from a 4T1 TNBC immunotherapy-resistant mouse model treated as in 3E and labeled with primary antibodies against CD45 and CD3 positive cells. Graphs plot the % cell population for each group ( n = 5 mice per group). Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns > 0.05. (H) FFPE sections were taken from primary tumors from a 4T1 TNBC immunotherapy-resistant mouse model treated as in 2D and labeled with primary antibodies against CD8, LSD1, TIGIT, LAG3, and TIM3. The CD8 + T cell population positive for these markers was analyzed using the ASI digital pathology system to enumerate % total cell population. Graphs plot the % cell population for either CD8 + T cell infiltration or CD8 + LSD1 + TIGIT + LAG3 + TIM3 + T cells ( N > 500 cells per group, 5 mice per group). Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns > 0.05. Treatment groups are control, abraxane (30 mg/kg), phenelzine (40 mg/kg), EPI-111 (1 mg/kg), EPI-111 (4 mg/kg), and EPI-111 (20 mg/kg), with 5 mice per group. (I) 4T1 breast cancer treatment regimen. Treatment groups from left to right. Control, abraxane (30 mg/kg), phenelzine (40 mg/kg), EPI-111 (4 mg/kg), and anti-PD1 (10 mg/kg). (J) FFPE sections were taken from primary tumors from a 4T1 TNBC immunotherapy-resistant mouse model treated as in 2D and labeled with primary antibodies against CD8. The CD8 + T cell population within the FFPE section was analyzed using the ASI digital pathology system to enumerate % total cell population. Graphs plot the % cell population for either CD8 + T cell infiltration ( N > 500 cells per group, n = 5 mice per group). Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns > 0.05. (K) FFPE sections were taken from primary tumors from a 4T1 TNBC immunotherapy-resistant mouse model treated as in 3J and labeled with primary antibodies against CD8 and IFN-γ. The CD8 + T cell population positive for both of these markers was analyzed using the ASI digital pathology system to enumerate % total double-positive cell population. Graphs plot the % cell population for CD8 + IFN-g + T cells ( n > 500 cells per group; n = 5 mice per group). Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns > 0.05.

Article Snippet: Liquid biopsies were pre-enriched using the RosetteSepTM method to isolate CD8 + T cells by employing the RosetteSepTM Human CD8 enrichment Kit (15063, Stemcell Technologies, Vancouver, Canada) to remove CD45 + cells and red blood cells using density gradient centrifugation with SepMateTM-15 (IVD) density gradient tubes (85420, Stemcell Technologies) and LymphoprepTM density gradient medium (07861, Stemcell Technologies).

Techniques: Inhibition, Gene Expression, Transformation Assay, Control, Isolation, Over Expression, Expressing, Reverse Transcription Polymerase Chain Reaction, Staining, Flow Cytometry, Labeling, MANN-WHITNEY

Journal: Frontiers in Immunology

Article Title: Targeting Nuclear LSD1 to Reprogram Cancer Cells and Reinvigorate Exhausted T Cells via a Novel LSD1-EOMES Switch

doi: 10.3389/fimmu.2020.01228

Figure Lengend Snippet: nLSD1p inhibition induces immune cell infiltration and re-invigoration and enhances Tm in CD8 + T cells in mouse models and humans. (A) CD8 + T cells from TNBC patients were untreated or treated with phenelzine, GSK, or control in vitro and stained with CCR7 and CD45RA antibodies to categorize them into naïve, T effector memory (Tem), and T effector memory RA (Temra). Cells were also stained with perforin and IFN-γ after stimulation with PMA/CaI for 4 h in the presence of brefeldin A. (B) t-distributed stochastic neighbor embedding (tSNE) analysis was performed on patient-derived TNBC CD8 + T cells either pre or post LSD1 therapy after PMA/ionomycin stimulation. Gated populations were divided into Naïve, Tscm, Tcm, Tem, and Temra phenotypes. (C) tSNE analysis was performed on patient-derived TNBC CD8 + T cells post LSD1 therapy or post 25 weeks LSD1 therapy after PMA/ionomycin stimulation. Gated populations (naïve, Tem, and Temra) of distinct phenotypes were overlaid onto a 2-dimensinal tSNE data space, revealing the differential expression of IFN-γ and perforin in total CD8 + T cells or different CD8 subsets.

Article Snippet: Liquid biopsies were pre-enriched using the RosetteSepTM method to isolate CD8 + T cells by employing the RosetteSepTM Human CD8 enrichment Kit (15063, Stemcell Technologies, Vancouver, Canada) to remove CD45 + cells and red blood cells using density gradient centrifugation with SepMateTM-15 (IVD) density gradient tubes (85420, Stemcell Technologies) and LymphoprepTM density gradient medium (07861, Stemcell Technologies).

Techniques: Inhibition, Control, In Vitro, Staining, Derivative Assay, Quantitative Proteomics

Journal: Frontiers in Immunology

Article Title: Targeting Nuclear LSD1 to Reprogram Cancer Cells and Reinvigorate Exhausted T Cells via a Novel LSD1-EOMES Switch

doi: 10.3389/fimmu.2020.01228

Figure Lengend Snippet: Global transcriptome analysis shows that phenelzine-mediated gene signatures are common to reinvigoration phenotypes in different model systems. (A) Volcano plot of the difference in gene expression before and after phenelzine treatment in TNBC and HER2 − donor CD8 + T cell transcriptomes. Significance was determined in DeSeq2, FDR < 0.1, n = 4. Three hundred fifty genes were downregulated with phenelzine (PHE) treatment and 314 were upregulated. (B) Enrichment of the down (PHE_Down) and up (PHE_UP) PHE signatures in different models of T cell exhaustion, activation, and memory. For x vs. y comparisons, a positive normalized enrichment score (NSE) indicates enrichment in x, a negative score enrichment in y. * p < 0.05 ** p < 0.01 *** p < 0.001. (C) Enrichment plots for GSE72752 and GSE24081 showing individual genes from the two phenelzine signatures distributed across the ranking in expression from chronic to resolver or progressor to controller. (D) Expression profiles of the genes up- and downregulated by phenelzine in the two donors (TNBC and HER2 − ). Averages of the duplicate isolations and treatments are shown ( n = 2). The number of SMAD (S) and HIC2 (H) or EOMES (E) and RUNX1 (R) motifs in nearby enhancers are marked. Upregulated genes with at least 5 SMAD motifs in nearby enhancers or that are negative regulators of the TGF-b pathway are named. Downregulated genes with at least 5 EOMES motifs in nearby enhancers are named (red: direct (bound) EOMES targets upregulated by EOMES overexpression; blue: direct (bound) targets downregulated by EOMES overexpression).

Article Snippet: Liquid biopsies were pre-enriched using the RosetteSepTM method to isolate CD8 + T cells by employing the RosetteSepTM Human CD8 enrichment Kit (15063, Stemcell Technologies, Vancouver, Canada) to remove CD45 + cells and red blood cells using density gradient centrifugation with SepMateTM-15 (IVD) density gradient tubes (85420, Stemcell Technologies) and LymphoprepTM density gradient medium (07861, Stemcell Technologies).

Techniques: Gene Expression, Activation Assay, Expressing, Over Expression

Journal: Frontiers in Immunology

Article Title: Targeting Nuclear LSD1 to Reprogram Cancer Cells and Reinvigorate Exhausted T Cells via a Novel LSD1-EOMES Switch

doi: 10.3389/fimmu.2020.01228

Figure Lengend Snippet: The EOMES:LSD1p nuclear complex is enriched in PD-1 + CD8 + T cells from resistant, high disease burden patients. (A) CD8 + T cells were isolated from healthy donors, melanoma patient cohorts, or metastatic breast cancer patient (ER + /PR + /HER2- or TNBC) liquid biopsies and labeled with primary antibodies targeting T-bet, EOMES, and PD-1. ASI Digital Pathology Analysis was carried out to calculate the percentage population of T-bet Low EOMES Hi PD-1 + T cells. Patient cohorts included n = 5 healthy donors, n = 20 patients in the responder cohort, and n = 15 patients in the resistant cohort, with sampling as in with 4 samples per patient. (B) Primary antibodies against LSD1 and EOMES were used to label PD-1 + CD8 + T cells from healthy donors or melanoma patients with different immunotherapy susceptibility profiles. Samples were processed by ASI Digital Pathology Analysis based on >500 cells (patient cohorts included n = 5 healthy donors, n = 20 patients in the responder cohort, and n = 15 patients in the resistant cohort, with sampling as in with 4 samples per patient). The % EOMES Hi LSD1 + PD-1 + CD8 + T cell population was analyzed for each group as well as the TNFI of LSD1 and EOMES. Representative images for each dataset are shown with scale bar = 10 mm. Graphs represent either the % cell population (positive for EOMES/LSD1) or the TNFI for LSD1 and EOMES measured using digital pathology (ASI) minus background ( n > 500 cells/patient sample for 40 patient samples). The EOMES:LSD1 PCC was determined for at least 40 individual cells ± SEM. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns p > 0.05. (C) Primary antibodies against LSD1 and EOMES were used to label PD-1 + CD8 + T cells from healthy donors or metastatic breast cancer patients (ER + /PR + /HER2 − or TNBC). Samples were processed by ASI digital pathology analysis based on >500 cells. Patient cohorts included n = 5 healthy donors, n = 20 patients in the responder cohort, and n = 15 patients in the resistant cohort, with sampling as in with 4 samples per patient. The % EOMES Hi LSD1 + PD-1 + CD8 + T cell population was analyzed for each group. Graphs represent the mean % positive cell population measured using digital pathology (ASI) minus background ( n > 500 cells/patient sample for 40 patient samples). The EOMES:LSD1 PCC was determined for at least 40 individual cells ± SEM. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns p > 0.05. (D) Proximity ligation assay (DuoLink) for EOMES and LSD1 in CD8 + T cells from melanoma patients with different immunotherapy susceptibility profiles. Representative images shown with scale bar = 10 mm. Graph plotted measures the PLA (ligation intensity measured by high-resolution microscopy) protein interaction. Patient cohorts = 3 patients per group and 4 repeat samples per patient. (E) Melanoma primary tumor baseline tissue biopsies for either responder or resistant melanoma patient cohorts were stained for LSD1, EOMES, and CD8 with DAPI. Representative images for each dataset are shown. Graphs represent either the % population of EOMES + LSD1 + CD8 + T cells or the mean TNFI for LSD1 and EOMES measured using ASI Digital Pathology minus background ( n > 50 cells/patient sample for 20 patient samples). The EOMES:LSD1 PCC was determined for at least 20 individual cells ± SEM. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns p > 0.05. n = 20 patient samples total; n = 10 responder patient samples, n = 10 resistant patient samples (with 4 repeat samples per patient). (F) Metastatic brain cancer lesions from a metastatic breast cancer patient were stained for LSD1, EOMES, and CD8 with DAPI. Representative images for each dataset are shown. Graphs represent the mean TNFI for LSD1 and EOMES measured using ASI Digital Pathology minus background ( n > 50 cells/patient sample for 30 patient samples). The EOMES:LSD1 PCC was determined for at least 20 individual cells ± SEM. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, * p = 0.033, ns p > 0.05.

Article Snippet: Liquid biopsies were pre-enriched using the RosetteSepTM method to isolate CD8 + T cells by employing the RosetteSepTM Human CD8 enrichment Kit (15063, Stemcell Technologies, Vancouver, Canada) to remove CD45 + cells and red blood cells using density gradient centrifugation with SepMateTM-15 (IVD) density gradient tubes (85420, Stemcell Technologies) and LymphoprepTM density gradient medium (07861, Stemcell Technologies).

Techniques: Isolation, Labeling, Sampling, MANN-WHITNEY, Proximity Ligation Assay, Ligation, Microscopy, Staining

Journal: Frontiers in Immunology

Article Title: Targeting Nuclear LSD1 to Reprogram Cancer Cells and Reinvigorate Exhausted T Cells via a Novel LSD1-EOMES Switch

doi: 10.3389/fimmu.2020.01228

Figure Lengend Snippet: An EOMES methylation/acetylation switch regulated by LSD1 in CD8 + T cells indicates immunotherapy responsiveness. (A) Jurkat T cells transfected with either VO, LSD1 wildtype (LSD1-WT), or LSD1 NLS mutant plasmids (LSD1-NLSmut) were probed with primary antibodies targeting EOMES and screened by IF. Graphs represent the TNFI and Fn/c for n = 20 or more cells ( n = 3 experiments). Mean NFI and Fn/c are shown. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, ns >0.05. (B) Schematic of EOMES plasmids and 641k motif. (C) Jurkat T cells transfected with either VO, EOMES-WT, EOMES-Mut1, or EOMES-Mut2 plasmids and probed with primary antibodies targeting EOMES and screened by IF. Graphs represent the TNFI and Fn/c for n = 20 or more cells ( n = 3 experiments). Representative images for each dataset are shown; scale bar indicates 10 μM. Mean NFI and Fn/c are shown. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, ns >0.05. (D) Nuclear extracts from jurkat T cells transfected with LSD1 WT or mutant plasmids and subjected to half-way CHIP using LSD1 pull down or a no antibody control. Samples were subject to immunoblot analysis and probed with a primary rabbit antibody to human EOMES; representative bands are shown. EOMES band intensity was plotted using ImageJ software minus background for n = 3 with mean ± SEM. Group 1, EOMES WT; Group 2, EOMES-Mut2; Group 3, LSD1 WT; Group 4, LSD1 NLS mutant. (E) EOMES plasmids and Jurkat T cells transfected with either VO, EOMES-WT, EOMES-Mut1, or EOMES-Mut2 plasmids and probed with antibodies targeting Ki67, IFN-γ, and TNF-α. Graphs show the percentage of cells calculated from ≥ 500 cells in 3 experiments ( n = 3) and the mean TFI of markers ( n ≥ 20 cells). Representative images for each dataset are shown; scale bar indicates 10 μM. Mean TFI and the population % are shown. Mann-Whitney test, **** p < 0.0001, *** p = 0.0002, ** p = 0.0021, ns >0.05. (F) EOMES protein structure showing the NLS and DNA-binding domain and the custom antibodies raised against specific PTMs. (G) Primary melanoma baseline biopsies classified as responder or resistant and processed for 3D high-resolution digital pathology with primary antibodies to CD8, EOMES-Ac, or EOMES-Me2 with DAPI. Representative images for each dataset are shown ( n ≥ 90 cells/sample). The % population of each target is plotted along with scale bar = 15 mm. n = 20 patient samples total; n = 10 responder patient samples, n = 10 resistant patient samples. (H) CD8 + T cells were isolated from healthy donors (HD) and immunotherapy resistant or responsive melanoma patients and screened by IF microscopy for (H) EOMES-641k-Ac or (I) EOMES-641k-Me2 or (J) EOMES-373k-Me2 and LSD1. For each LSD1:EOMES pair, the PCC was determined ( n = 10 patients, ≥20 cells/patient). Both the nuclear and cytoplasmic fluorescence intensity of each marker are plotted with significant differences indicated as well as the Fn/c; Mann-Whitney test, **** p < 0.0001, ** p = 0.0021, ns>0.05. IF microscopy patient cohorts included n = 5 healthy donors, n = 15 patients in the responder cohort, and n = 15 patients in the resistant cohort, with sampling as in with 4 samples per patient. (I) CD8 + T cells were isolated from healthy donors (HD), immunotherapy resistant or responsive melanoma patients and screened by IF microscopy for EOMES-641k-Me2 and LSD1. For each LSD1:EOMES-641k-Me2 pair, the PCC was determined ( n = 10 patients per group, ≥20 cells/patient). Both the nuclear and cytoplasmic fluorescence intensities of each marker are plotted with significant differences indicated as well as the Fn/c; Mann-Whitney test, **** p < 0.0001, ** p = 0.0021, * p < 0.05, ns>0.05. IF microscopy patient cohorts included n = 5 healthy donors, n = 15 patients in the responder cohort, and n = 15 patients in the resistant cohort, with sampling as in with 4 samples per patient. (J) CD8 + T cells were isolated from healthy donors (HD) and immunotherapy resistant or responsive melanoma patients and screened by IF microscopy for EOMES-373k-Me2 and LSD1. For each LSD1:EOMES-373k-Me2 pair, the PCC was determined ( n = 10 patients per group, ≥20 cells/patient). Both the nuclear and cytoplasmic fluorescence intensities of each marker are plotted with significant differences indicated as well as the Fn/c; Mann-Whitney test, **** p < 0.0001, ** p = 0.0021, * p < 0.05, ns>0.05. IF microscopy patient cohorts included n = 5 healthy donors, n = 15 patients in the responder cohort, and n = 15 patients in the resistant cohort, with sampling as in with 4 samples per patient. (K) IF microscopy was performed on 4T1 syngeneic metastatic cancer model-derived CD8 + T cells fixed and probed with antibodies targeting EOMES-641k-Ac and CD8 or EOMES-641k-Me2 and CD8 with DAPI. >10,000 cells/group were scanned to profile the % positive population of infiltrating CD8 + T cells in the primary tumor microenvironment for each EOMES marker ( n = 5 mice per group). Significant differences between groups are indicated as per the Mann-Whitney test, **** p < 0.0001, ** p = 0.0021, ns>0.05.

Article Snippet: Liquid biopsies were pre-enriched using the RosetteSepTM method to isolate CD8 + T cells by employing the RosetteSepTM Human CD8 enrichment Kit (15063, Stemcell Technologies, Vancouver, Canada) to remove CD45 + cells and red blood cells using density gradient centrifugation with SepMateTM-15 (IVD) density gradient tubes (85420, Stemcell Technologies) and LymphoprepTM density gradient medium (07861, Stemcell Technologies).

Techniques: Methylation, Transfection, Mutagenesis, MANN-WHITNEY, Control, Western Blot, Software, Binding Assay, Isolation, Microscopy, Fluorescence, Marker, Sampling, Derivative Assay

Journal: Scientific Reports

Article Title: LSD1 activation promotes inducible EMT programs and modulates the tumour microenvironment in breast cancer

doi: 10.1038/s41598-017-17913-x

Figure Lengend Snippet: LSD1 correlates with MBC CTC mesenchymal- and CSC-like characteristics. ( a ) CTCs were isolated from MBC patient liquid biopsies through double expression of cytokeratin (CK) and vimentin (VIM) and absence of CD45 expression on the DEPArray. Representative image from DEPArray and workflow shown. ( b ) CD45 − /VIM + /CK + CTC cell counts were determined in two samples collected six weeks apart (sample 1 and sample 2, respectively) (n = 10). ( c ) Immunofluorescence microscopy was performed on all fixed CTCs collected from 10 MBC patients at each time point and compared to normal donors. Representative images showing DAPI staining in CTCs is shown (n = 5 healthy donors and 10 MBC patients). ( d ) CTCs were separated based on LSD1-s111p TNFI relative to negative controls, primary and secondary antibody controls as well as healthy donor expression into phenotypes 1, 2 and 3 (high, moderate and low expression, respectively) and Snail TNFI and CSV TCFI were determined (n = 10). Representative images are shown for each dataset. ( e ) Average percentage of phenotype 1, 2 and 3 cells (n = 10). ( f ) CTCs were separated based on LSD1 TNFI relative to negative controls, primary and secondary antibody controls as well as healthy donor expression into phenotypes 1, 2 and 3 (high, moderate and low expression, respectively) and ALDH1A TNFI and ABCB5 TNFI were determined (n = 10). Representative image is shown for each dataset. ( g ) Average percentage of phenotype 1, 2 and 3 cells (n = 10). ( h ) Graph depicts the PCC for LSD1 and ALDH1A (n = 10). −1 = inverse of colocalization; 0 = no colocalization; +1 = perfect colocalization. ( i ) Graph depicts LSD1-s111p TNFI, CSV TCFI and CD45 − /VIM + /CK + CTC cell count in five samples collected at indicated time points. Representative images are shown for each time point (n = 1 patient). Isolated CTCs were treated with either vehicle alone, pargyline or phenelzine and then immunofluorescence microscopy or qPCR was performed. Total florescence intensity of CSV and LSD1-s111p and Snail after treatment with ( j ) pargyline; or ( k ) phenelzine (n > 75 cells from 10 patients). ( l ) ALDH1 TNFI after treatment with pargyline or phenelzine (n = 20 cells from 10 patients). ( m ) VIM and CD44 mRNA transcript levels after treatment with pargyline or phenelzine (n = 10 pooled). Scale bars = 10 μM. ns = p > 0.05; *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001, Mann-Whitney test.

Article Snippet: Liquid biopsies were pre-enriched using the RosetteSepTM method to isolate CTCs by employing the RosetteSepTM Human CD45 Depletion Kit (15162, Stemcell Technologies) to remove CD45 + cells and red blood cells, using density gradient centrifugation with SepMateTM-15 (IVD) density gradient tubes (85420, Stemcell Technologies) and LymphoprepTM density gradient medium (07861, Stemcell Technologies).

Techniques: Isolation, Expressing, Immunofluorescence, Microscopy, Staining, Cell Counting, MANN-WHITNEY

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: IL13-eGFP mice were treated with 3 doses of rIL-33 (1μg per dose), Alt (10μg) or PBS (25μl) over 1 week and culled 24h after the final dose. The frequency of ILC2 (GFP+ CD45+ Linneg CD3-NKp46-CD127+CD90.2+KLRG1+CD25varIL-13+IL-5+) in the (A) airways (BAL fluid), (B) lung and (C) lung draining lymph nodes (mediastinal). Live viable precision cut lung slices of 200μm thickness were obtained and stained for CD31 (Magenta, the lung structure and blood vessels), CD4 (cyan, T cells, orange arrow), EpCAM (Red, to visualise bronchial epithelium) and GFP (ILC2, white arrow). Images of 1024μm x 1024μm field of view (FOV) were taken under a 20x objective using an inverted confocal microscope. (D) Images showing ILC2 (GFP+CD4-) CD4+ T cells (CD4+GFP-) location in PBS, rIL-33 and Alt treated mice, scale bar, 150 μm. (E) Number of ILC2 (GFP+CD4-) in lung sections per FOV taken under a 10x objective. (F) Schematic illustration of the lung depicting the anatomical location in the lung where precision cut lung slices were prepared. Representative images show two regions of the lung slice from a rIL-33 treated mouse showing distribution of ILC2 and CD4+ T cells, scale bar 150 μm. n = 4 mice per group (Mock(PBS)), n= 6 mice per group (Alt or rIL-33 treatment). Data representative of 4 experiments. *p < 0.05, **p < 0.01, ***p <0.001 and, **** p < 0.0001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: Staining, Microscopy

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: IL13-eGFP mice were treated with 3 doses of rIL-33 (1μg per dose), over 1 week and culled 24h after the final dose. Live viable precision cut lung slices (PCLS) of 200μm thickness were obtained and stained for CD31 (Magenta, the lung structure and blood vessels), CD4 (cyan, T cells, orange arrow), EpCAM (Red, to visualise bronchial epithelium) and GFP (ILC2, white arrow), and time-lapse video taken (1024μm x 1024μm field of view (FOV), 45 min duration under a 20x objective using an inverted confocal microscope) (A) Static image depicting the location of ILC2 and CD4+ T cells, scale bar 100 μm. (B) Zoomed in section of the blood vessel in figure 2A, scale bar 20 μm. (C) High power images of boxed cells in figure 2B showing differences in pattern of cell movement (oscillatory vs amoeboid movement). ILC2 and CD4+ T cells dynamics were tracked and plotted as (D) individual tracks or (E) tracks commencing from centroid and overlaid. (F) Track speed, (G) track length and (H) track displacement were quantified. Representative images shown in (A-C) are from rIL-33 treated mice, where n = 6 mice per treatment (3 slices per mouse were imaged). For (F-H) in box and whiskers plots, each dot represents an individual cell. Data are representative from 4 experiments where n = 6 mice per treatment. *p < 0.05, **p < 0.01, ***p < 0.001 and, **** p < 0.0001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: Staining, Microscopy

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: IL13-eGFP mice were treated with 3 doses of rIL-33 (1μg per dose) or Alt (10μg) over 1 week. Live precision cut lung slices were obtained and ILC2 dynamics were compared between the two and the differences were plotted as (A) individual tracks and (B) tracks commencing from centroid and overlaid. Differences in tracks between treatments were quantified as (C) track speed, (D) track length and (E) track displacement. Intravital microscopy (IVM) was performed in live IL-13eGFP mice after rIL-33 treatment (one 512μm x 512μm field of view (FOV) in a 1-hour-duration video). (F) Static images of different frames captured during the course of the video depicting amoeboid shape changes of ILC2 at separate time-points, scale bar 20 μm. n ≥ 4 mice per group. Data representative of 4 experiments. *p < 0.05, **p < 0.01, ***p < 0.001 and, **** p < 0.0001. Quantifications from (A-E) are representative of 4 experiments, where n = 6 mice per treatment (3 slices per mouse were imaged). For (F) IVM images are representative of 6 individual IL-33 treated mice. *p < 0.05, **p < 0.01, ***p < 0.001, and, **** p < 0.0001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: Intravital Microscopy

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: IL13-eGFP mice were treated with 3 doses of rIL-33 (1μg per dose) or PBS (25μl), over 1 week and culled 24h after the final dose. (A) The percentage of murine ILC2 (CD45+LinnegNKp46-CD3-) expressing CCR1, CCR4 and CCR8. CCL8 levels in murine (B) BAL and (C) lung. (D) Location of CCL8 expression and ILC2 and (E) quantified CCL8 deposits in PCLS stained for CD31 (Magenta, the lung structure and blood vessels), CCL8 (cyan, yellow arrow), EpCAM (Red, to visualise bronchial epithelium) and GFP (ILC2, white arrow), images of 1024μm x 1024μm FOV, scale bar 150 μm. Human ILC2 lines were generated and migration to varying concentrations of (F) PGD2 and (G) CCL8 were determined. (H) Peak migratory responses of a human ILC2 cell line to IL-25, TGF-β, rIL-33, CCL8 and PGD2. IL13-eGFP mice treated with rIL-33 were also treated with 5μg purified anti-mouse CCR8 antibody i.p., rCCL8 i.n. or an isotype control and PCLS obtained and stained. (I) Localisation of ILC2 in live PCLS. (J) Number of ILC2 per FOV under 10x objective. Time-lapse imaging of 45 min duration was performed and ILC2 (K) track from centroid, (L) track length and (M) track speed and (N) track displacement were quantified. In box and whiskers graphs each data point represents an individual cell. Balb/c mice treated with rIL-33 were further treated with rCCL8, αCCR8 or Isotype control antibody. (O) Percentage of IL-13+IL-5+ILC2 (CD45+lin-NKp46-CD3-GATA-3+). (P) Representation Histogram of MFI of IL-13 and IL-5 and quantification of MFI for (Q) IL-13 and (R) IL-5 from GATA+ ILC2. For panels A-E n ≥ 4 mice per group. Data representative of 4 experiments. For panels F-H n = 3 individual donors. Data representative of 3 experiments. For panels I-R, n = 5 mice per group. Data representative of 2 experiments *p < 0.05, **p < 0.01, ***p < 0.001 and,**** p < 0.0001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: Expressing, Staining, Generated, Migration, Purification, Control, Imaging

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: Human ILC2 lines were seeded on tissue culture plates coated with either 10% FBS, fibronectin, collagen-I, collagen-IV or serum free coating (control) for 24h. Cell movement was imaged via the JuLI imaging system and plotted as (A) individual tracks, (B) track speed dot plots and (C) track speed spider plot. IL13-eGFP mice were treated with 3 doses of rIL-33 (1μg per dose) or PBS (25μl), over 1 week and culled 24h after the final dose PCLS obtained. (D) SHG imaging of PCLS revealing collagen fibres, representative maximum intensity projections, scale bar 50μm. (E) GLCM analysis of SHG imaging. (F) Images of Fibronectin expression and localisation. PCLS stained for CD31 (Magenta, the lung structure and blood vessels), Fibronectin (cyan, yellow arrow), EpCAM (Red, to visualise bronchial epithelium) and GFP (ILC2, white arrow) and images of 1024μm x 1024μm field of view (FOV) were taken, scale bar 150μm. For panels A-C, n = 3 donors (in triplicate). Data representative of 3 experiments. For panels D-F n = 6 (in triplicate). *p < 0.05, **p < 0.01, ***p < 0.001 and,****, ****P < 0.0001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: Control, Imaging, Expressing, Staining

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: Human ILC2 lines were seeded on tissue culture plates coated with either 10% FBS, fibronectin, collagen-I, collagen-IV or serum free coating (control) and imaged after 12 hours. (A) Bright field images depicting change in shape. (B) Actin remodelling following staining with Phalloidin (green) and DAPI (cyan) and imaging using Airyscan detection (maximum intensity projections), scale bar 5μm. (C) Cell area. (D) Cell perimeter. n = 3 donors. Data representative of 2 experiments. *** P < 0.001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: Control, Staining, Imaging

Journal: Science immunology

Article Title: Pulmonary environmental cues drive group 2 innate lymphoid cell dynamics in mice and humans

doi: 10.1126/sciimmunol.aav7638

Figure Lengend Snippet: IL13-eGFP mice treated with rIL-33 were further treated with (BAPN) along with controls were culled 24 hours after the final dose. ILC2 dynamics from live PCLS were plotted as either (A) individual tracks or (B) tracks commencing from centroid and overlaid. Differences in tracks between treatments were quantified as (C) track speed, (D) track length and (E) track displacement. Total ILC2 () in (F) Lungs, (G) BAL and (H) Blood were enumerated. For panels A-E n ≥ 4 mice per group. Data representative of 4 experiments. For panels F-H n = 6 mice per group. Data representative of 2 experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001.

Article Snippet: ILC2 were enriched from whole blood using RosetteSepTM Human ILC2 Enrichment Kit (STEMCELL Technologies) and further sorted by FACs using CD45 + Lineage neg (CD1a, CD3, CD4, CD5, CD8, CD11c, CD14, CD16, CD19, CD20, CD34, FcγRI and CD123) (Biolegend), CD161 + , CD127 + , CRTH2 + and C-Kit var (Biolegend).

Techniques: