促炎细胞因子
库普弗电池
胰岛素抵抗
活检
肝活检
表型
生物
分离(微生物学)
胰岛素
内分泌学
内科学
病理
医学
免疫学
生物信息学
炎症
基因
生物化学
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 11-13
标识
DOI:10.1007/978-1-0716-0704-6_2
摘要
Liver macrophages (LMs) are phagocytic cells that play an important role in many liver disorders due to their ability to respond to a variety of stimuli and activating signals. It is currently debated whether LMs activation from an anti-inflammatory to a proinflammatory phenotype contributes to obesity-induced metabolic diseases. We recently found that LMs can produce noninflammatory factors, such as the protein IGFBP7, able to directly regulate hepatic glucose production and lipidLipids accumulation in the liverLiver. However, while in a mouseMouse model of obesity and insulinInsulin resistance LM-Igfbp7 expression is pathologically increased, in obese insulin-resistant patients LM-IGFBP7 is edited at RNA level independently of an effect on its expression. This discrepancy between results in animals and humans confirms the importance to perform molecular investigation directly on humanHuman’s isolated cellsCells. Here, we describe a protocol to isolate liverLiver macrophagesMacrophages from humanHuman liverLiver biopsy Biopsies .
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