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Image Search Results
Journal: Chinese Medical Journal
Article Title: Role of the Ca 2+ -Calcineurin-Nuclear Factor of Activated T cell Pathway in Mitofusin-2-Mediated Immune Function of Jurkat Cells
doi: 10.4103/0366-6999.223855
Figure Lengend Snippet: Effect of MFN2 on intracellular calcium, calcineurin expression, and NFAT activity in Jurkat cells. Jurkat cells were transfected with LV-MFN2 and MFN2-RNAi and then stimulated with PMA (50 ng/ml) plus ionomycin (1 mmmol/L) for various lengths of time. (a and c) Intracellular calcium was measured by FACS with the fluorescent probe Fluo-3/AM. (b) Calcineurin activity was measured using a calcineurin assay kit. (d) NFAT activity in Jurkat cells was measured by ELISA. * P < 0.05, † P < 0.01 versus the control group; ‡ P < 0.05, § P < 0.01 versus the control-RNAi or LV-GFP group. LV: Lentiviral vector; MFN2: Mitofusin-2; GFP: Green fluorescent protein; NFAT: Nuclear factor of activated T cells; PMA: Phorbol myristate acetate.
Article Snippet: Nuclear extract and
Techniques: Expressing, Activity Assay, Transfection, Enzyme-linked Immunosorbent Assay, Control, Plasmid Preparation
Journal: Chinese Medical Journal
Article Title: Role of the Ca 2+ -Calcineurin-Nuclear Factor of Activated T cell Pathway in Mitofusin-2-Mediated Immune Function of Jurkat Cells
doi: 10.4103/0366-6999.223855
Figure Lengend Snippet: Regulation of calcineurin expression reverses MFN2-induced NFAT activation in Jurkat cells. After various pretreatments, Jurkat cells were stimulated with PMA plus ionomycin for 24 h. Jurkat cells were pretreated with MFN2-RNAi and then LV-calcineurin, and calcineurin activity was measured by commercial assay kit (a) and NFAT activity was determined by ELISA (c). Jurkat cells were pretreated with LV-MFN2 and then FK-506, and calcineurin activity (b) and NFAT activity (d) were measured. * P < 0.05 vs. the control group; † P < 0.05 vs. the control-RNAi or LV-GFP group; ‡ P < 0.05 vs. the LV-MFN2 or MFN2-RNAi group. LV: Lentiviral vector; MFN2: Mitofusin-2; GFP: Green fluorescent protein; NFAT: Nuclear factor of activated T-cell. P/I: PMA (phorbol myristate acetate)/ionomycin; ELISA: Enzyme-linked immunosorbent assay.
Article Snippet: Nuclear extract and
Techniques: Expressing, Activation Assay, Activity Assay, Enzyme-linked Immunosorbent Assay, Control, Plasmid Preparation
Journal: Free radical biology & medicine
Article Title: The HIV-Tat protein interacts with Sp3 transcription factor and inhibits its binding to a distal site of the sod2 promoter in human pulmonary artery endothelial cells
doi: 10.1016/j.freeradbiomed.2019.12.015
Figure Lengend Snippet: Using an Sp-specific oligonucleotide-binding ELISA (TransAm, Active Motif), we measured the levels of active Sp1 (Panel A) and Sp3 (Panel B) in the nucleus of mock transfected (Tat(−)) or pCP2-Tat101 transfected (Tat(+)) HPAEC. The signal was normalized to μg of nuclear protein. Mean ± SEM of biological replicates, n = 3, (***p ≤ 0.001 by unpaired student’s T-test).
Article Snippet: DNA-binding ELISAs for active Sp1 and Sp3 were carried out on nuclear extracts prepared as previously described [ 21 ] using Sp1 and Sp3-specific
Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay, Transfection