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1.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 23-8, 2014.
Article in English | WPRIM | ID: wpr-636505

ABSTRACT

The effect of thymic stromal lymphopoietin (TSLP) on macrophage-derived foam cell formation and the underlying mechanism were studied. Macrophages isolated from C57BL/6 mice were co-cultured in vitro with different concentrations of TSLP or TSLPR-antibody in the presence of oxidized low density lipoprotein (ox-LDL). The effects of TSLP on macrophage-derived foam cell formation were observed by using oil red O staining and intracellular lipid determination. The expression levels of foam cell scavenger receptors (CD36 and SRA) as well as ABCA1 and TSLPR were detected by using RT-PCR and Western blotting. As compared with the control group, TSLP treatment significantly promoted lipid accumulation in macrophages, significantly increased protein expression of CD36 and TSLPR in a dose-dependent manner, and significantly reduced the expression of ABCA1 protein in a dose-dependent manner. No significant differences were noted between the TSLPR-antibody group and the control group. TSLP may down-regulate the expression of cholesterol efflux receptor ABCA1 and up-regulate scavenger receptor expression via the TSLPR signaling pathway, thereby promoting macrophage-derived foam cell formation.

2.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 23-28, 2014.
Article in English | WPRIM | ID: wpr-251366

ABSTRACT

The effect of thymic stromal lymphopoietin (TSLP) on macrophage-derived foam cell formation and the underlying mechanism were studied. Macrophages isolated from C57BL/6 mice were co-cultured in vitro with different concentrations of TSLP or TSLPR-antibody in the presence of oxidized low density lipoprotein (ox-LDL). The effects of TSLP on macrophage-derived foam cell formation were observed by using oil red O staining and intracellular lipid determination. The expression levels of foam cell scavenger receptors (CD36 and SRA) as well as ABCA1 and TSLPR were detected by using RT-PCR and Western blotting. As compared with the control group, TSLP treatment significantly promoted lipid accumulation in macrophages, significantly increased protein expression of CD36 and TSLPR in a dose-dependent manner, and significantly reduced the expression of ABCA1 protein in a dose-dependent manner. No significant differences were noted between the TSLPR-antibody group and the control group. TSLP may down-regulate the expression of cholesterol efflux receptor ABCA1 and up-regulate scavenger receptor expression via the TSLPR signaling pathway, thereby promoting macrophage-derived foam cell formation.


Subject(s)
Animals , Mice , ATP Binding Cassette Transporter 1 , Genetics , Metabolism , Antibodies , Allergy and Immunology , Pharmacology , Blotting, Western , CD36 Antigens , Genetics , Metabolism , Cells, Cultured , Cholesterol , Metabolism , Cholesterol Esters , Metabolism , Cytokines , Pharmacology , Dose-Response Relationship, Drug , Foam Cells , Cell Biology , Metabolism , Gene Expression , Immunoglobulins , Allergy and Immunology , Metabolism , Lipoproteins, LDL , Pharmacology , Macrophages , Cell Biology , Metabolism , Mice, Inbred C57BL , Receptors, Cytokine , Allergy and Immunology , Metabolism , Reverse Transcriptase Polymerase Chain Reaction , Scavenger Receptors, Class A , Genetics , Metabolism
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