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dc.contributor.authorRojas-Jaimes, J.
dc.contributor.authorPelaez, L.C.
dc.date.accessioned2025-10-31T18:37:25Z
dc.date.available2025-10-31T18:37:25Z
dc.date.issued2023
dc.identifier.urihttps://hdl.handle.net/20.500.12805/5519
dc.description.abstractBackground: Multinucleated giant cells were first described by Langhans(MGCs), these MGCs have a role in innate immunity that includes extracellular matrix remodeling associated with granuloma formation; another function of them is to participate in the removal of cellular debris in apoptosis during certain infections. Objective: Generate multinucleated giant cells due to Leishmania (V.) braziliensis infection. Methods: For infection macrophage/parasite ratio of 1 to 10 using the RAW 264.7-line (5 x105/mL) and Leishmania (V.) braziliensis metacyclic promastigotes (50 x105/mL) was a strain maintained in culture Schneider liquid medium, supplemented with 20% fetal bovine serum and 10 000 U/10 mg/mL penicillin streptomycin at pH 7 and 25 °C in the laboratory. Incubation was continued for 4 days, and microscopic observation at 1000X was performed at 24 hours and 96 hours, respectively. Results: In our study an MGC conversion was observed at 96 hours (50% ± 28.2). Conclusions: In vitro MGC model could be used to study the physiopathology of MGC generation by Leishmania (V.) braziliensis infection.en_US
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherEManuscript Technologies
dc.relation.ispartofurn:issn:0975-3575
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectMacrophage Responses in Tuberculosis and Protein Interactionsen_US
dc.subjectCytokine Influence on Multinucleated Giant Cell Formationen_US
dc.titleGeneration of Multinucleated Giant Cells due to Leishmania (V.) braziliensis Infectionen_US
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.doihttps://doi.org/10.5530/pj.2023.15.172
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.03.07
dc.type.otherResearch article
dc.identifier.journalPharmacognosy Journal
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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