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Image Search Results
Journal: Communications Biology
Article Title: NUPR1 protects against hyperPARylation-dependent cell death
doi: 10.1038/s42003-022-03705-1
Figure Lengend Snippet: a OXPHOS metabolism, reflected by oxygen consumption rate (OCR) levels were measured in MiaPaCa-2 cells after 24 h treatments. b MiaPaCa-2 cells were treated with ZZW-115 (1.5 µM) and olaparib (25 µM) for 24 h, then, loaded with MitoTracker Deep-Red FM and, after fixation, stained with DAPI. Flow cytometry analysis were carried out using MitoProbe™ TMRM ( c ), MitoSOX™ Red ( d ), CellROX™ Orange Reagent ( e ) or Fluo-4-AM ( f ) for analysis of the mitochondrial membrane potential, mitochondrial superoxide levels, intracellular ROS levels and the cytosolic calcium concentration, respectively, after 24 h of incubation with the drugs. Data represent mean ± SEM. Two-way, Sidak was used, * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.001. g PLA was performed in MiaPaCa-2 cells in the presence or in the absence of ZZW-115 together or not with 5-FU in the presence or absence of olaparib. Mouse anti-PAR and rabbit anti-Mitofusin2 antibodies were used. A representative experiment is shown ( n = 3). ImageJ was used to count the number of green dots. Mean ± SEM of foci/nucleus are included.
Article Snippet: Finally, samples were mounted using the
Techniques: Staining, Flow Cytometry, Membrane, Concentration Assay, Incubation
Journal: Journal of Innate Immunity
Article Title: Prognostic Value and Therapeutic Potential of TREM-1 in Streptococcus pyogenes- Induced Sepsis
doi: 10.1159/000348283
Figure Lengend Snippet: S. pyogenes induces expression of TREM-1 in BMDM. a Expression of trem-1 mRNA on BMDM after infection with S. pyogenes at MOI of 1:1, 10:1 and 100:1 bacteria per macrophage. BMDM were exposed to S. pyogenes for 1 h, washed and further incubated in the presence of gentamicin for 4 h. Total RNA was isolated followed by RT-PCR analysis of trem-1 and β-actin gene expression. b Quantitative expression of trem-1 mRNA on BMDM after infection with S. pyogenes at MOI of 1:1, 10:1 and 100:1 bacteria per macrophage measured by real-time PCR. c Fluorescence microscope photographs of TREM-1 in BMDM infected with S. pyogenes at MOI of 1:1 (cii), 10:1 (ciii) and 100:1 (civ) bacteria per macrophage. TREM-1 expression on uninfected macrophages is also shown (ci). TREM-1 appears in red and S. pyogenes in green. Macrophage nuclei are stained by DAPI (blue). Bar = 25 µm.
Article Snippet: Coverslips were washed with PBS, mounted on glass slides with Mowiol containing
Techniques: Expressing, Infection, Bacteria, Incubation, Isolation, Reverse Transcription Polymerase Chain Reaction, Gene Expression, Real-time Polymerase Chain Reaction, Fluorescence, Microscopy, Staining