焦磷酸香叶基香叶基
辛伐他汀
结肠炎
他汀类
焦磷酸法尼酯
生物
MAPK/ERK通路
预酸化
甲戊酸途径
药理学
ABCA1
信号转导
内分泌学
内科学
免疫学
医学
细胞生物学
还原酶
生物化学
酶
基因
生物合成
运输机
作者
Mahesh Pandit,Suman Acharya,Ye Gu,Sang‐Uk Seo,Mi‐Na Kweon,Ben Kang,Jae‐Hoon Chang
标识
DOI:10.1002/eji.202048991
摘要
Abstract Blocking the mevalonate pathway for cholesterol reduction by using statin may have adverse effects including statin‐induced colitis. Moreover, one of the predisposing factors for colitis is an imbalanced CD4 + T cell, which can be observed on the complete deletion of HMG‐CoA reductase (HMGCR), a target of statins. In this study, we inquired geranylgeranyl pyrophosphate (GGPP) is responsible for maintaining the T‐cell homeostasis. Following dextran sulfate sodium (DSS)‐induced colitis, simvastatin increased the severity of disease, while cotreatment with GGPP, but not with cholesterol, reversed the disease magnitude. GGPP ameliorated DSS‐induced colitis by increasing T reg cells. GGPP amplified T reg differentiation through increased IL‐2/STAT 5 signaling. GGPP prenylated Ras protein, a prerequisite for extracellular signal‐regulated kinase (ERK) pathway activation, leading to increased IL‐2 production. Higher simvastatin dose increased the severity of colitis. GGPP ameliorated simvastatin‐increased colitis by increasing T reg cells. T reg cells, which have the capacity to suppress inflammatory T cells and were generated through IL‐2/STAT5 signaling, increased IL‐2 production through prenylation and activation of the Ras/ERK pathway.
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