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(A) Confocal Microscopy images of microglial <t>ASC</t> in brain sections from cortices of male 5XFAD mice injected with either Scr or Anti-17 MLNPs. Brain sections were stained with microglial marker IBA1 (Green) and ASC (red), and nuclei with DAPI (blue). N = 3 Scr MLNPs and 3 Anti-17 MLNPs injected mice. Unpaired t -test was used for statistical analysis. *P < 0.05 . (B &C) The volume of ASC in the cortex and ASC colocalized with microglia (IBA1) were measured using Imaris software from z-stack images of 5XFAD injected mice brains. N = 3, t -test was used for statistical analysis, *P < 0.05 . (D) ASC Immunoblot of microglia (CD11b+) isolated from male and female 5XFAD injected mice, β-Actin was used as a loading control. N = 3 males and N = 2 females. (E) Relative copy numbers (RCN) of Asc from brains of 5XFAD mice injected with either Scr or Anti-17 MLNPs. N = 3, unpaired t -test was used for statistical analysis, ***P < 0.001 , (F) Immunoblots for ASC from brain homogenates of WT and 5XFAD mice either Anti-17 or Scr MLNPs injected for 4 weeks. M (Male) and F (Female) (G) Densitometry for ASC in F was performed using ImageJ software and normalized to β-Actin. N = 3, One-way ANOVA was used for statistical analysis.
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(A) Confocal Microscopy images of microglial <t>ASC</t> in brain sections from cortices of male 5XFAD mice injected with either Scr or Anti-17 MLNPs. Brain sections were stained with microglial marker IBA1 (Green) and ASC (red), and nuclei with DAPI (blue). N = 3 Scr MLNPs and 3 Anti-17 MLNPs injected mice. Unpaired t -test was used for statistical analysis. *P < 0.05 . (B &C) The volume of ASC in the cortex and ASC colocalized with microglia (IBA1) were measured using Imaris software from z-stack images of 5XFAD injected mice brains. N = 3, t -test was used for statistical analysis, *P < 0.05 . (D) ASC Immunoblot of microglia (CD11b+) isolated from male and female 5XFAD injected mice, β-Actin was used as a loading control. N = 3 males and N = 2 females. (E) Relative copy numbers (RCN) of Asc from brains of 5XFAD mice injected with either Scr or Anti-17 MLNPs. N = 3, unpaired t -test was used for statistical analysis, ***P < 0.001 , (F) Immunoblots for ASC from brain homogenates of WT and 5XFAD mice either Anti-17 or Scr MLNPs injected for 4 weeks. M (Male) and F (Female) (G) Densitometry for ASC in F was performed using ImageJ software and normalized to β-Actin. N = 3, One-way ANOVA was used for statistical analysis.
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(A) Confocal Microscopy images of microglial ASC in brain sections from cortices of male 5XFAD mice injected with either Scr or Anti-17 MLNPs. Brain sections were stained with microglial marker IBA1 (Green) and ASC (red), and nuclei with DAPI (blue). N = 3 Scr MLNPs and 3 Anti-17 MLNPs injected mice. Unpaired t -test was used for statistical analysis. *P < 0.05 . (B &C) The volume of ASC in the cortex and ASC colocalized with microglia (IBA1) were measured using Imaris software from z-stack images of 5XFAD injected mice brains. N = 3, t -test was used for statistical analysis, *P < 0.05 . (D) ASC Immunoblot of microglia (CD11b+) isolated from male and female 5XFAD injected mice, β-Actin was used as a loading control. N = 3 males and N = 2 females. (E) Relative copy numbers (RCN) of Asc from brains of 5XFAD mice injected with either Scr or Anti-17 MLNPs. N = 3, unpaired t -test was used for statistical analysis, ***P < 0.001 , (F) Immunoblots for ASC from brain homogenates of WT and 5XFAD mice either Anti-17 or Scr MLNPs injected for 4 weeks. M (Male) and F (Female) (G) Densitometry for ASC in F was performed using ImageJ software and normalized to β-Actin. N = 3, One-way ANOVA was used for statistical analysis.

Journal: Brain, behavior, and immunity

Article Title: Microglia-targeted inhibition of miR-17 via mannose-coated lipid nanoparticles improves pathology and behavior in a mouse model of Alzheimer’s disease

doi: 10.1016/j.bbi.2024.05.006

Figure Lengend Snippet: (A) Confocal Microscopy images of microglial ASC in brain sections from cortices of male 5XFAD mice injected with either Scr or Anti-17 MLNPs. Brain sections were stained with microglial marker IBA1 (Green) and ASC (red), and nuclei with DAPI (blue). N = 3 Scr MLNPs and 3 Anti-17 MLNPs injected mice. Unpaired t -test was used for statistical analysis. *P < 0.05 . (B &C) The volume of ASC in the cortex and ASC colocalized with microglia (IBA1) were measured using Imaris software from z-stack images of 5XFAD injected mice brains. N = 3, t -test was used for statistical analysis, *P < 0.05 . (D) ASC Immunoblot of microglia (CD11b+) isolated from male and female 5XFAD injected mice, β-Actin was used as a loading control. N = 3 males and N = 2 females. (E) Relative copy numbers (RCN) of Asc from brains of 5XFAD mice injected with either Scr or Anti-17 MLNPs. N = 3, unpaired t -test was used for statistical analysis, ***P < 0.001 , (F) Immunoblots for ASC from brain homogenates of WT and 5XFAD mice either Anti-17 or Scr MLNPs injected for 4 weeks. M (Male) and F (Female) (G) Densitometry for ASC in F was performed using ImageJ software and normalized to β-Actin. N = 3, One-way ANOVA was used for statistical analysis.

Article Snippet: Membranes were incubated overnight with antibodies against human beta-amyloid (Cell signaling technology, 8243S), mouse ASC (Cell signaling technology, 67824), and GAPDH (Cell Signaling Technology, 2118).

Techniques: Confocal Microscopy, Injection, Staining, Marker, Software, Western Blot, Isolation, Control

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Journal: EMBO Molecular Medicine

Article Title: Navigating from cellular phenotypic screen to clinical candidate: selective targeting of the NLRP3 inflammasome

doi: 10.1038/s44321-024-00181-4

Figure Lengend Snippet: Reagents and tools table

Article Snippet: Rabbit anti-mouse ASC , Adipogen , AG-25B-0006-C100 (pAL177).

Techniques: Knock-Out, Expressing, Recombinant, Plasmid Preparation, Enzyme-linked Immunosorbent Assay, Western Blot, Software, Microscopy