Cytokine profile and phagocytic capacity of Ndufs4−/− macrophages [Dataset]

(A, B) Parental (Par), and Ndufs4−/− RAW 264.7 cells were left untreated or treated with LPS (100 ng/ml). Supernatants were collected at 8 hours for measurement of cytokine concentrations by ELISA (A). Cells were collected at 4 hours for quantification of cytokine transcripts using real-time PCR (ex...

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Detalles Bibliográficos
Autores: Serrano-Lorenzo, Pablo, Gobelli, Dino, Garrido-Moraga, Rocío, Esteban-Amo, María J., López-López, José R., Orduña, Antonio, Fuente, Miguel A. de la, Martín, Miguel Ángel, Simarro-Grande, María
Tipo de recurso: conjunto de datos
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/352276
Acceso en línea:http://hdl.handle.net/10261/352276
Access Level:acceso abierto
Palabra clave:Leigh syndrome patients
Inflammatory cytokine profile
Increasing evidence demonstrate
Div >< p
Mitochondrial respiration alterations
Macrophage effector functions
Effector functions
Maximal respiration
Vitro </
Supernumerary subunit
Shift towards
Phagocytose gram
Ndufs4 </
Mutational hotspot
Modulatory role
Lower levels
Lipopolysaccharide challenge
Improved ability
Critical role
Atp production
Descripción
Sumario:(A, B) Parental (Par), and Ndufs4−/− RAW 264.7 cells were left untreated or treated with LPS (100 ng/ml). Supernatants were collected at 8 hours for measurement of cytokine concentrations by ELISA (A). Cells were collected at 4 hours for quantification of cytokine transcripts using real-time PCR (expressed as fold increases versus untreated parental cells) (B). (C) Representative flow cytometry plots (left) showing phagocytosis of FITC labeled heat killed E. coli (HKEC) and bar graph representing % of fluorescent cells and the MFI values (right). Ctrl, control. Ns, not significant; *, P <0.05; **, P <0.01; ***, P<0.005; ****, P<0.001. Each point represents a biological replicate. In all experiments, 4 to 5 different Ndufs4−/− clones were used. Data are shown as the mean ± SEM.

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