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DC Field | Value | Language |
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dc.contributor.author | Kumar, Ashish | - |
dc.contributor.author | Naik, Lincoln | - |
dc.contributor.author | Patel, Salina | - |
dc.contributor.author | Das, Mousumi | - |
dc.contributor.author | Nayak, Dev Kiran | - |
dc.contributor.author | Mishra, Abtar | - |
dc.contributor.author | Mishra, Amit | - |
dc.contributor.author | Singh, Ramandeep | - |
dc.contributor.author | Behura, Assirbad | - |
dc.contributor.author | Dhiman, Rohan | - |
dc.date.accessioned | 2022-12-14T06:24:54Z | - |
dc.date.available | 2022-12-14T06:24:54Z | - |
dc.date.issued | 2022-11 | - |
dc.identifier.citation | 49th Annual Conference of Indian Immunology Society (Immunocon-2022), PGIMER, Chandigarh, 23-26 November 2022 | en_US |
dc.identifier.uri | http://hdl.handle.net/2080/3799 | - |
dc.description | Copyright belongs to proceeding publisher | en_US |
dc.description.abstract | Introduction: Ac-93253 iodide induces apoptosis in NSCLC cancer cells. Our study found that it is bactericidal against Mycobacterium tuberculosis (M.tb), and it induces apoptosis upon treatment of non-cytotoxic concentration. Due to the primary finding, we want to decipher the mechanism of apoptosis and its effect on the survival of intracellular mycobacteria human macrophages. Methods: We have checked the expression of apoptosis-inducing genes and proteins through qRT-PCR and western blotting in Ac-93253 treated and mycobacterial-infected dTHP-1 cells. To confirm the apoptosis, We isolate DNA fragments and analyze them through agarose gel electrophoresis. To validate the above findings, we have used Annexin V and propidium iodide staining to check the accumulation of phosphatidylserine in the plasma membrane's outer leaflet. To quantify the loss of ∆ m we used Rhodamine 123 staining, and stained cells were analyzed through flow cytometry. To validate the role of ∆ m, we used cyclosporine A1 and checked its effect on apoptosis and anti-mycobacterial activity. To understand the canonical pathway of apoptosis, we checked the secretion of TNFα through sandwich ELISA. Result: Through MTT and trypan blue exclusion assay, 0.5 μM of Ac-93253 was found to be non-cytotoxic even after 72 hours of treatment in phorbol 12-myristate 13-acetate (PMA) differentiated THP-1 (dTHP-1) cells. Significant up-regulation in the expression of various pro-apoptotic genes like Bcl-2, Bax, and Bad and the cleaved caspase 3 was observed upon treatment with a non-cytotoxic dose of Ac93253. Ac-93253 treatment also leads to DNA fragmentation and increased phosphatidylserine accumulation in the outer leaflet of the plasma membrane. Ac-93253 treatment also effectively reduced the intracellular growth of mycobacteria in infected dTHP-1 cells, and ZVAD-FMK broad-range apoptosis inhibitor significantly brought back the intracellular mycobacterial growth in Ac-93253 treated macrophages. Conclusion: These findings suggest apoptosis may be the probable effector response through which Ac-93253 manifests its antimycobacterial property | en_US |
dc.subject | mycobacteria | en_US |
dc.subject | human macrophages | en_US |
dc.subject | apoptosis | en_US |
dc.subject | Tuberculosis (TB) | en_US |
dc.title | Ac-93253 Inhibits Intracellular Growth of Mycobacteria in Human Macrophages by Inducing Apoptosis in Mitochondrial-Dependent Manner | en_US |
dc.type | Presentation | en_US |
Appears in Collections: | Conference Papers |
Files in This Item:
File | Description | Size | Format | |
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2022_IMMUNOCON_AKumar_AC-93253.pdf | Poster | 1.14 MB | Adobe PDF | View/Open |
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