DAPI (Invitrogen) was used at 300 nM to identify cellular nuclei. Sections were mounted by using Fluorogel (Electron Microscopy Services). selleck chemicals All sections were imaged using either a Nikon Eclipse 80i microscope or an Olympus BX-51

microscope. Three TBI animals were analyzed and at least five sections per animal were analyzed. For gene expression profiling of macrophages from YARG mice, Arg1+ (YFP+ CD45hi CD11b+ Ly6G− SYTOX Blue−) and Arg1− macrophages (YFP− CD45hi CD11b+ Ly6G− SYTOX Blue−) were isolated by flow cytometry from ipsilateral brain hemispheres at day 1 following TBI (n = 4 for each cell sample). Monocytes (CD11b+ F4/80+) from peripheral blood were also collected. Sorted cells were immediately lysed in denaturation buffer and frozen. RNA was isolated by using an RNAqueous Micro kit (Ambion). Further sample preparation, labeling, and array hybridizations were performed according to standard protocols from the UCSF Shared Microarray Core Facilities and Agilent Technologies. RNA quality was assessed using a Pico Chip on an Agilent 2100 Bioanalyzer (Agilent Technologies), and RNA was amplified by use of a whole transcriptome

amplification kit (Sigma-Aldrich). Ceritinib datasheet Subsequent Cy3-CTP labeling was performed by using a NimbleGen one-color labeling kit (Roche-NimbleGen, Inc.). The quality of the amplified products was assessed by using an Agilent 2100 Bioanalyzer and Nanodrop ND-8000 (Nanodrop Technologies, Inc.). Fossariinae The products were hybridized to Agilent whole mouse genome 4×44K microarrays according to the manufacturer’s protocol. Arrays were scanned with an Agilent microarray scanner, and raw signal intensities were extracted with Feature Extraction v10.5 software. Data were normalized by using the quantile normalization method [54]. No background subtraction was performed,

and the median feature pixel intensity was used as the raw signal before normalization. A one-way ANOVA linear model was fitted to the comparison to estimate the false discovery rate for each gene for the comparison of interest, and genes with a false discovery rate < 0.05 were considered significant. Scatter plots compared averaged log2 gene expression from each group. PCA was performed using the top 15% of genes exhibiting the most variance across all samples, using the PopulationDistances module of GenePattern (PMID: 16642009). For heatmaps, data were log2 transformed and median centered across genes. Replicates were hierarchically clustered (PMID: 16939791). Heatmaps of genes selected from the top 15% most variable genes that exhibited interesting pairwise comparisons were visualized using Java Treeview (http://sourceforge.net/projects/jtreeview/files/) (PMID: 15180930). Meta-analysis of transcriptional responses of brain wound macrophages to BMDMs stimulated by either IFN-γ or IL-4 was performed using previously published tables [38].