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Image Search Results
Journal: Cell death & disease
Article Title: RhoA balances microglial reactivity and survival during neuroinflammation.
doi: 10.1038/s41419-023-06217-w
Figure Lengend Snippet: Fig. 5 Inflammation disrupts Ca2+, pH, and mitochondrial homeostasis in RhoA-deficient microglia. A Lifeact fluorescence labeling in RhoA WT, RhoA T19N, or RhoA KO HMC3 microglia (n = 3 independent experiments). B Cell counting in RhoA WT, RhoA Q63L, RhoA T19N, or RhoA KO HMC3 microglia (n = 8 independent experiments). Graph displays mean with SD. ****p < 0.0001 (Two-way ANOVA). RhoA WT, RhoA T19N, or RhoA KO HMC3 microglia expressing a global Ca2+ biosensor (C), mitochondrial Ca2+ biosensor (D), endoplasmic reticulum Ca2+ biosensor (E), pH biosensor (F), MitoTimer biosensor (G), or mitophagy biosensor (H) and exposed to LPS (1 µg/ml; 20 min (C-F) or 60 min (G and H)). Graphs (mean and SD) display fluorescence changes (n = 15 cells per group from 3 independent experiments for each biosensor). *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 (Two-way ANOVA). Scale bars: 20 µm.
Article Snippet: Raichu-RhoA (provided by M. Matsuda [27]), pTriEx-RhoA FLARE.sc Biosensor WT (RRID:Addgene_12150), pTriEx-RhoA FLARE.sc Biosensor Q63L (RRID:Addgene_12151),
Techniques: Labeling, Cell Counting, Expressing
Journal: Cell death & disease
Article Title: RhoA balances microglial reactivity and survival during neuroinflammation.
doi: 10.1038/s41419-023-06217-w
Figure Lengend Snippet: Fig. 2 RhoA regulates microglial metabolic reprogramming during inflammation. HMC3 microglia expressing the ATP biosensor (A), Glucose biosensor (B), Lactate biosensor (C), or Pyruvate biosensor (D) were transfected with RhoA Q63L (red) or RhoA WT (blue) and exposed to LPS (1 µg/ml; 20 min) (n = 15-30 cells per group from 3 independent experiments for each biosensor). Primary cortical microglia expressing the ATP biosensor (E) or Lactate biosensor (F) were transfected with the RhoA Q63L (red) or RhoA WT (blue) and exposed to LPS (1 µg/ml; 20 min) (n = 6 cells per group from 3 independent experiments for each biosensor). Panels are time-lapse ratio images coded according to the pseudocolor ramps. Graphs (means and SD) display F490/F435 (A and E), FRET/Donor (B), and Donor/FRET (C, D, and F) ratio change at 0 (CT) and 20 min. G Seahorse measurements of bioenergetic parameters in HCM3 microglia expressing RhoA Q63L or RhoA WT. The parameters were calculated based on the OCR following the sequential addition of LPS, oligomycin, FCCP, rotenone, and antimycin A. Results are from at least 3 independent experiments. Graphs show the mean with SD. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 (Two-way ANOVA). Scale bars: 20 µm.
Article Snippet: Raichu-RhoA (provided by M. Matsuda [27]), pTriEx-RhoA FLARE.sc Biosensor WT (RRID:Addgene_12150),
Techniques: Expressing, Transfection
Journal: Cell death & disease
Article Title: RhoA balances microglial reactivity and survival during neuroinflammation.
doi: 10.1038/s41419-023-06217-w
Figure Lengend Snippet: Fig. 3 RhoA regulates microglial proinflammatory reactivity. HMC3 microglia expressing a ROS biosensor (A), AMPK biosensor (B), ERK biosensor (C), Src biosensor (D), and GFP-tagged p65 NFkB subunit (E) were transfected with the RhoA Q63L construct or with RhoA WT and then exposed to LPS (1 µg/ml for 20 min) (n = 18–100 cells per group from 3 independent experiments for each biosensor). Panels show time- lapse ratio images or mean fluorescent intensity (MFI) coded according to the pseudocolor ramps. F ELISA (TNF-α or IL-1ß) from culture supernatants of primary cortical microglia transfected with RhoA Q63L or RhoA WT and exposed to LPS (1 µg/ml) for 3 h (n = 4 independent experiments). Graphs are means with SD. *p < 0.05, ***p < 0.001, ****p < 0.0001 (Two-way ANOVA). Scale bars: 20 µm.
Article Snippet: Raichu-RhoA (provided by M. Matsuda [27]), pTriEx-RhoA FLARE.sc Biosensor WT (RRID:Addgene_12150),
Techniques: Expressing, Transfection, Construct, Enzyme-linked Immunosorbent Assay
Journal: Cell death & disease
Article Title: RhoA balances microglial reactivity and survival during neuroinflammation.
doi: 10.1038/s41419-023-06217-w
Figure Lengend Snippet: Fig. 5 Inflammation disrupts Ca2+, pH, and mitochondrial homeostasis in RhoA-deficient microglia. A Lifeact fluorescence labeling in RhoA WT, RhoA T19N, or RhoA KO HMC3 microglia (n = 3 independent experiments). B Cell counting in RhoA WT, RhoA Q63L, RhoA T19N, or RhoA KO HMC3 microglia (n = 8 independent experiments). Graph displays mean with SD. ****p < 0.0001 (Two-way ANOVA). RhoA WT, RhoA T19N, or RhoA KO HMC3 microglia expressing a global Ca2+ biosensor (C), mitochondrial Ca2+ biosensor (D), endoplasmic reticulum Ca2+ biosensor (E), pH biosensor (F), MitoTimer biosensor (G), or mitophagy biosensor (H) and exposed to LPS (1 µg/ml; 20 min (C-F) or 60 min (G and H)). Graphs (mean and SD) display fluorescence changes (n = 15 cells per group from 3 independent experiments for each biosensor). *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 (Two-way ANOVA). Scale bars: 20 µm.
Article Snippet: Raichu-RhoA (provided by M. Matsuda [27]), pTriEx-RhoA FLARE.sc Biosensor WT (RRID:Addgene_12150),
Techniques: Labeling, Cell Counting, Expressing