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KMID : 0923620090090030098
Immune Network
2009 Volume.9 No. 3 p.98 ~ p.105
Cordycepin Suppresses Expression of Diabetes Regulating Genes by Inhibition of Lipopolysaccharide-induced Inflammation in Macrophages
Shin Seul-Mee

Lee Sung-Won
Kwon Jeong-Hak
Moon Sun-Hee
Lee Seung-Jeong
Lee Chong-Kil
Cho Kyung-Hae
Ha Nam-Joo
Kim Kyung-Jae
Abstract
Background: It has been recently noticed that type 2 diabetes (T2D), one of the most common metabolic diseases, causes a chronic low-grade inflammation and activation of the innate immune system that are closely involved in the pathogenesis of T2D. Cordyceps militaris, a traditional medicinal mushroom, produces a component compound, cordycepin (3¡¯-deoxyadenosine). Cordycepin has been known to have many pharmacological activities including immunological stimulating, anti-cancer, and anti-infection activities. The molecular mechanisms of cordycepin in T2D are not clear. In the present study, we tested the role of cordycepin on the anti-diabetic effect and anti-inflammatory cascades in LPS-stimulated RAW 264.7 cells.

Methods: We confirmed the levels of diabetes regulating genes mRNA and protein of cytokines through RT-PCR and western blot analysis and followed by FACS analysis for the surface molecules.

Results: Cordycepin inhibited the production of NO and pro-inflammatory cytokines such as IL-1¥â, IL-6, and TNF-¥á in LPS-activated macrophages via suppressing protein expression of pro-inflammatory mediators. T2D regulating genes such as 11¥â-HSD1 and PPAR¥ã were decreased as well as expression of co-stimulatory molecules such as ICAM-1 and B7-1/-2 were also decreased with the increment of its concentration. In accordance with suppressed pro-inflammatory cytokine production lead to inhibition of diabetic regulating genes in activated macrophages. Cordycepin suppressed NF-¥êB activation in LPS-activated macrophages.

Conclusion: Based on these observations, cordycepin suppressed T2D regulating genes through the inactivation of NF-¥êB dependent inflammatory responses and suggesting that cordycepin will provide potential use as an immunomodulatory agent for treating immunological diseases.
KEYWORD
cordycepin, type 2 diabetes, pro-inflammatory cytokines, immunomodulator
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