| Literature DB >> 26986202 |
Zhenying Han, Fanxia Shen, Yue He, Vincent Degos, Marine Camus, Mervyn Maze, William L Young, Hua Su.
Abstract
Entities:
Year: 2016 PMID: 26986202 PMCID: PMC4795596 DOI: 10.1371/journal.pone.0152218
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 5PHA decreased pro-inflammatory microglia/macrophages (M1).
A: Representative images of M1 (CD11b+Iba-1+) staining. The nuclei were counterstained with DAPI. Scale bar: 50 μm. B: Quantification of M1 in the peri-infarct region. *: p<0.001, vs. saline group at corresponding time points. C: Representative images of M2 (CD206+Iba-1+) staining. The nuclei were counterstained with DAPI. Scale bar: 50 μm. D: Quantification of M2 microglia/macrophages in the peri-infarct region. *: p<0.001 vs. saline group on D3 after pMCAO. E: The ratios of M1 and M2 cells. *: p<0.001, #: p = 0.018 vs. saline group 3 days after pMCAO; and &: p = 0.015, δ: p = 0.009 vs. saline group 14 days after pMCAO.
Fig 3PHA reduced lesion volume and TUNEL+ neurons.
A: Representative images of cresyl violet-stained sections on D3 and D14 after pMCAO. Scale bar: 1 mm. B: Quantification of infarct volume on D3. *: p = 0.009, #: p = 0.001 vs. saline group. C: Quantification of atrophy volume on D14 after pMCAO. *: p = 0.008 vs. corresponding saline groups. D: A cresyl violet-stained coronal section (bregma 1.3 mm, top, scale bar: 1 mm) and a TUNEL-stained section (bottom, scale bar: 50 um). Black squares in the cresyl violet-stained section show the areas used for quantification of NeuN+/TUNEL+ cells. Infarct border is shown in the TUNEL-stained section. E: Representative images of NeuN and TUNEL-stained sections. F: Quantification of NeuN and TUNEL double positive cells. *: p = 0.001, #: p<0.001 vs. saline group.