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1.
J Leukoc Biol ; 115(1): 1-3, 2024 01 05.
Artigo em Inglês | MEDLINE | ID: mdl-37931143

RESUMO

Mechanisms of regulating the beneficial and harmful capabilities of neutrophils include IL-10/IL-10RA signaling in neutrophils that limits clearance of Streptococcus pneumoniae and accumulation of neutrophils in pneumonic lung tissue.


Assuntos
Pneumonia , Streptococcus pneumoniae , Humanos , Neutrófilos/fisiologia , Interleucina-10 , Pulmão
2.
Integr Biol (Camb) ; 4(11): 1428-36, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23064132

RESUMO

Quantification of 3D morphology and measurement of cellular functions were performed on the mouse melanoma cell lines of B16F10 to investigate the intriguing problem of structure-function relations in the genetically engineered cells with GPR4 overexpression. Results of 3D analysis of cells in suspension and phase contrast imaging of adherent cells yield consistent evidence that stimulation of the proton-sensing GPR4 receptor in these cells may modify significantly their morphology with diminishing ability to produce membrane protrusions and to migrate. Examination of the 3D parameters of mitochondria provide further insights on the measured variation of the maximal capacity of oxygen consumption rate among the genetically modified cells, indicating that the proton-sensing receptor may regulate cancer cell metabolism with increased mitochondrial surface area. Our study demonstrates clearly the significant benefits of quantitative 3D morphological study in illuminating cellular functions and development of novel morphology based cell assay methods.


Assuntos
Melanoma Experimental/patologia , Melanoma Experimental/fisiopatologia , Animais , Adesão Celular , Linhagem Celular Tumoral , Movimento Celular , Engenharia Genética , Proteínas de Fluorescência Verde/genética , Proteínas de Fluorescência Verde/metabolismo , Imageamento Tridimensional , Melanoma Experimental/genética , Camundongos , Microscopia Confocal , Mitocôndrias/metabolismo , Consumo de Oxigênio , Receptores Acoplados a Proteínas G/genética , Receptores Acoplados a Proteínas G/fisiologia , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismo
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