Fig. 2From: Intracerebral transplantation of interleukin 13-producing mesenchymal stem cells limits microgliosis, oligodendrocyte loss and demyelination in the cuprizone mouse modelPhenotypic analysis of the different macrophage and microglia populations in BFP-MSC and IL13-MSC grafts in the CNS of eGFP+ bone marrow chimaeras. a Overview of a BFP-MSC and IL13-MSC graft, showing MHCII-expressing (blue) and Arg1-expressing (red) microglia and macrophages. Scale bars indicate 200Ā Ī¼m. Details of the BFP-MSC and IL13-MSC implant and border are provided, showing graft-infiltrating macrophages (green) in combination with Arg1- (red) and MHCII-expressing (blue) microglia and macrophages. Scale bars indicate 50Ā Ī¼m. The following cell populations can be distinguished: eGFP+MHCII+Arg1ā macrophages (cyan), eGFP+MHCIIāArg1+ macrophages (yellow), eGFP+MHCII+Arg1+ macrophages (white), eGFP+MHCIIāArg1ā macrophages (green), eGFPāMHCII+Arg1ā microglia (blue), eGFPāMHCIIāArg1+ microglia (red), eGFPāMHCII+Arg1+ microglia (magenta). eGFPāMHCIIāArg1ā microglia (black background) cannot be visualised using this setup. Dotted lines delineate the actual implants. The border area is an area extending 85Ā Ī¼m from the implant. b Cell densities of all different cellular phenotypes characterised within the implant site (upper graph) and in the implant border (lower graph) of BFP-MSC and IL13-MSC grafts. Values are given as meanā+āstandard deviation. Significant differences are indicated with one (p value <0.05), two (p value ā¤0.01) or three (p value ā¤0.001) asterisks. c Pie graphs showing mean representation of each microglia and macrophage phenotype within the BFP-MSC and IL13-MSC graft and border. For the graft site, the fraction of BFP-MSC or IL13-MSC is indicated. For the border, the fraction of other cells is indicated (*neurons, oligodendrocytes and/or astrocytes). The colours of differentially activated microglia and macrophage correspond to those in Fig.Ā 2a Back to article page