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Activation of PPARalpha Attenuates IFNgamma and IL-1beta-induced Cell Proliferation in Astrocytes: Involvement of IL-6 Independent Pathway
The Korean Journal of Physiology and Pharmacology ; : 185-189, 2010.
Article in English | WPRIM | ID: wpr-727801
ABSTRACT
The present study demonstrates the effect of fibrates, agonists of PPARalpha on cytokines-induced proliferation in primary cultured astrocytes. Alone or combination treatment with cytokines, such as IL-1beta (10 ng/ml), IFNgamma (10 ng/ml), and TNF-alpha (10 ng/ml) cause a significant increase of cell proliferation in a time-dependent manner. Treatment of astrocytes with bezafibrate and fenofibrate (0, 5, and 10 micrometer) reduced the IFNgamma and IL-1beta-induced cell proliferation in a dose-dependent manner. To address the involvement of IL-6 on the IFNgamma and IL-1beta-induced cell proliferation, released IL-6 level was measured. IFNgamma and IL-1beta cause an increase of released IL-6 protein level in a time-dependent manner. Furthermore, pretreatment with IL-6 antibody (0, 0.1, 1, 2.5, and 5 ng/ml) dose-dependently inhibited the IFNgamma and IL-1beta-induced cell proliferation. However, bezafibrate and fenofibrate did not affect increased mRNA and protein levels of IL-6 in IFNgamma and IL-1beta-stimulated astrocytes. Taken together, these results clearly suggest that activation of PPARalpha attenuates the IFNgamma and IL-1beta-induced cell proliferation through IL-6 independent pathway.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Fenofibrate / Bezafibrate / RNA, Messenger / Astrocytes / Cytokines / Interleukin-6 / Tumor Necrosis Factor-alpha / PPAR alpha / Cell Proliferation / Fibric Acids Language: English Journal: The Korean Journal of Physiology and Pharmacology Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Fenofibrate / Bezafibrate / RNA, Messenger / Astrocytes / Cytokines / Interleukin-6 / Tumor Necrosis Factor-alpha / PPAR alpha / Cell Proliferation / Fibric Acids Language: English Journal: The Korean Journal of Physiology and Pharmacology Year: 2010 Type: Article