首页|Adra1a调节LPS诱导的Lbp-/-小鼠原代肝细胞炎症反应

Adra1a调节LPS诱导的Lbp-/-小鼠原代肝细胞炎症反应

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目的 探究Adra1a调节LPS诱导的LBP敲除小鼠(Lbp-/-)原代肝细胞炎症反应。方法 利用二步灌流法提取WT型、Lbp-/-型小鼠原代肝细胞,构建由LPS诱发的原代肝细胞原发炎症模型;采用加入抑制剂哌唑嗪、转染siRNA来下调LBP敲除小鼠原代肝细胞Adra1a的表达;抑制剂法将原代肝细胞分为3组分别是对照组A、LPS组A、抑制剂哌唑嗪组,转染siRNA主要是对原代肝细胞进行分组,包括对照组B、LPS组B、si-NC组、si-Adra1a组;将WT型小鼠的原代肝细胞分为两组分别为对照组(空白对照)、LPS组(LPS刺激12 h)。本研究以WT型、Lbp-/-型小鼠原代肝细胞为研究对象利用Western blot方法验证Adra1a在LPS刺激下的变化情况,采用CCK-8、qRT-PCR、Western blot等实验方法验证哌唑嗪及si-Adra1a对Lbp-/-小鼠的原代肝细胞的炎症及存活率的改善情况。结果 在LPS刺激下Lbp-/-小鼠的原代肝细胞Adra1a蛋白表达显著升高(P<0。01),而野生型没有显著变化;抑制剂哌唑嗪组及干扰组的细胞存活率显著升高(P<0。01,P<0。05);抑制剂哌唑嗪组及si-Adra1a组的TNF-α、IL-1β炎症因子表达情况显著降低(P<0。01),与细胞损伤及炎症相关的蛋白p-p38、p-ERK、p-JNK的表达量也显著降低(P<0。01)。结论 LPS刺激Lbp-/-小鼠原代肝细胞后Adra1a表达上调、炎症信号因子上调,使用哌唑嗪与si-Adra1a 特异性降低Adra1a表达后使LPS相关的Lbp-/-小鼠原代肝细胞炎症因子明显下降,可验证敲除LBP导致Adra1a在LPS诱导的炎症调节中参与反应。
Adra1a regulates LPS-induced inflammation in primary hepatocytes of Lbp-/-mice
Objective To explore the role of Adra1a in regulating the LPS-induced inflammation response in primary hepatocytes of lipopolysaccharide-binding protein knockout(Lbp-/-)mice.Methods Primary hepatocytes were extracted from WT and Lbp-/-mice using a two-step perfusion method,and an inflammation model was established using LPS induction.Expression of Adra1a in primary hepatocytes of Lbp-/-mice was suppressed by administering the inhibitor prazosin and transfection with si-Adra1a.The cells were divided into three groups under inhibitor conditions:control group A,LPS group A,and prazosin group.For siRNA transfection,cells were also divided into groups:control group B,LPS group B,si-NC group,and si-Adra1a group.WT primary hepatocytes were divided into two groups:control group(blank)and LPS group(12 h stimulation).Changes in the Adra1a response to LPS stimulation were verified by Western blot.Other method ologies,such as CCK-8,qRT-PCR,and Western blot assays,were used to confirm improvements in cell inflammation and the survival rate by prazosin and si-Adra1a.Results Significant elevation in Adra1a protein expression in Lbp-/-primary hepatocytes was observed post-LPS stimulation(P<0.01),whereas no notable change was found in the wildtype.A remarkable increase in the cell survival rate was noted in prazosin and si-Adra1a groups(P<0.01,P<0.05).Furthermore,prazosin and si-Adra1a groups exhibited significantly reduced expression of proinflammatory factors TNF-αand IL-1 β(P<O.01),p-p38,p-ERK,and p-JNK(P<0.01),which are associated with cell damage and inflammation.Conclusions Following LPS stimulation,upregulation of Adra1a and proinflammatory cytokine expression was observed in Lbp-/-primary hepatocytes.Specific downregulation of Adra1a expression using prazosin and si-Adra1a significantly decreased LPS-induced proinflammatory cytokines in Lbp-/-primary hepatocytes.Adra1a is implicated in the regulation of the LPS-induced inflammation response in primary hepatocytes of Lbp-/-mice.

Adra1aLbp-/-miceprimary hepatocytesprazosinRNAiMAPK signaling pathway

米传靓、付彬、李思迪、陈志达、郭中坤、王可洲

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山东第一医科大学(山东省医学科学院)实验动物学院(省实验动物中心),济南 250117

济南朋悦实验动物繁育有限公司,济南 250000

肾上腺素受体α1A型受体 Lbp-/小鼠 原代肝细胞 哌唑嗪 干扰RNA MAPK信号通路

山东省医科院医药卫生科技创新工程项目济南市科技局"高校20条"项目山东省医药卫生科技发展计划山东省生猪产业技术体系建设项目

2021GXRC0112019WS177SDAIT-08-17

2024

中国比较医学杂志
中国实验动物学会,中国医学科学院医学实验动物研究所

中国比较医学杂志

CSTPCD北大核心
影响因子:0.473
ISSN:1671-7856
年,卷(期):2024.34(5)