Figure 5.
CNS cGVHD is associated with resident microglia proliferation and activation and donor-derived macrophage infiltration. (A) Allogeneic transplantation model for the delivery of 5 × 106 TCD BM from C57Bl/6 (H2b) donors expressing eGFP under the Csf1r promoter (B6.Csf1r-eGFP) with no T cells or with 0.5 × 106 CD3+ T cells into lethally irradiated B6D2F1 (H2b/d) recipients. (B-F) Representative confocal images of parenchymal brain regions of interest in GVHD and TCD mice, showing Iba1+ microglia/macrophages, GFP+ donor BMDMs, and merged images counterstained with 4’,6-diamidino-2-phenylindole (DAPI; cell nuclei). Green arrows identify donor-derived (GFP+) macrophages, and white arrows indicate resident (GFP−) microglia. Stereological quantification of each region shows the total Iba1+ cell population alongside the number of GFP+ donor BMDMs. (B) Meninges at days 35 and 100 after transplant. Original magnification ×40; scale bar, 30 μm. (C) Choroid plexus at days 35 and 100 posttransplantation. Original magnification ×40; scale bar, 30 μm. Dashed lines outline choroid plexus in the lateral ventricle adjacent to surrounding tissue. (D) Cortex at days 35 and 100 after transplant. Original magnification ×20; scale bar, 50 μm. (E) Hippocampal dentate gyrus at days 35 and 100 after transplant. Original magnification ×20; scale bar, 50 μm. (F) Habenula at days 35 and 100 after transplant. Original magnification ×40; scale bar, 30 μm. Data presented as mean ± standard error of the mean (n = 4-5 mice per group). Statistical differences calculated with unpaired Student t test. *P < .05, **P < .01, ***P < .001, ****P < .0001.

CNS cGVHD is associated with resident microglia proliferation and activation and donor-derived macrophage infiltration. (A) Allogeneic transplantation model for the delivery of 5 × 106 TCD BM from C57Bl/6 (H2b) donors expressing eGFP under the Csf1r promoter (B6.Csf1r-eGFP) with no T cells or with 0.5 × 106 CD3+ T cells into lethally irradiated B6D2F1 (H2b/d) recipients. (B-F) Representative confocal images of parenchymal brain regions of interest in GVHD and TCD mice, showing Iba1+ microglia/macrophages, GFP+ donor BMDMs, and merged images counterstained with 4’,6-diamidino-2-phenylindole (DAPI; cell nuclei). Green arrows identify donor-derived (GFP+) macrophages, and white arrows indicate resident (GFP) microglia. Stereological quantification of each region shows the total Iba1+ cell population alongside the number of GFP+ donor BMDMs. (B) Meninges at days 35 and 100 after transplant. Original magnification ×40; scale bar, 30 μm. (C) Choroid plexus at days 35 and 100 posttransplantation. Original magnification ×40; scale bar, 30 μm. Dashed lines outline choroid plexus in the lateral ventricle adjacent to surrounding tissue. (D) Cortex at days 35 and 100 after transplant. Original magnification ×20; scale bar, 50 μm. (E) Hippocampal dentate gyrus at days 35 and 100 after transplant. Original magnification ×20; scale bar, 50 μm. (F) Habenula at days 35 and 100 after transplant. Original magnification ×40; scale bar, 30 μm. Data presented as mean ± standard error of the mean (n = 4-5 mice per group). Statistical differences calculated with unpaired Student t test. *P < .05, **P < .01, ***P < .001, ****P < .0001.

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