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Image Search Results
Journal: Frontiers in Immunology
Article Title: Inhibition of complement activation by CD55 overexpression in human induced pluripotent stem cell derived kidney organoids
doi: 10.3389/fimmu.2022.1058763
Figure Lengend Snippet: iPSCs are vulnerable to complement activation. (A) HLA-ABC surface protein expression measured by flow cytometry in unstained (US), unstimulated (–) and IFN-γ stimulated (+) iPSCs. A representative histogram is shown of three independent experiments (n=3). (B) mRNA expression of CD46, CD55 and CD59 in iPSCs measured by RT-qPCR (n=3). (C) Complement inhibitor CD46, CD55 and CD59 protein surface expression in iPSCs measured by flow cytometry. Representative histograms are shown of three independent experiments (n=3). (D) Schematic of the experimental procedure to measure complement deposition on iPSCs in vitro . (E) C3 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C3 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C3 + proportion. (F) C5b-9 deposition on iPSCs incubated with heat-inactivated (dNHS) or active normal human serum (NHS) measured by flow cytometry. Results are presented as relative mean fluorescence intensity (MFI) and C5b-9 + proportion. A representative histogram of three independent experiments (n=3) is shown and indicates the gate for the C5b-9 + proportion. Error bars show standard deviation and significance (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001) was evaluated using T-test.
Article Snippet: For flow cytometry the following antibodies were used:
Techniques: Activation Assay, Expressing, Flow Cytometry, Quantitative RT-PCR, In Vitro, Incubation, Fluorescence, Standard Deviation