[1]牟歌,王晓敏,熊吉,等.PACS-2在非酒精性脂肪性肝病动态变化及意义[J].第三军医大学学报,2013,35(07):609-613.
 Mu Ge,Wang Xiaomin,Xiong Ji,et al.Dynamic expression and significance of PACS-2 in non-alcoholic fatty liver disease[J].J Third Mil Med Univ,2013,35(07):609-613.
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PACS-2在非酒精性脂肪性肝病动态变化及意义(/HTML )
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《第三军医大学学报》[ISSN:1000-5404/CN:51-1095/R]

卷:
35卷
期数:
2013年第07期
页码:
609-613
栏目:
论著
出版日期:
2013-04-15

文章信息/Info

Title:
Dynamic expression and significance of PACS-2 in non-alcoholic fatty liver disease
作者:
牟歌王晓敏熊吉冯吉李砚陈潇迪王斌魏艳玲王军陈东风
第三军医大学大坪医院野战外科研究所消化内科;新疆维吾尔自治区人民医院干部保健中心
Author(s):
Mu Ge Wang Xiaomin Xiong Ji Feng Ji Li Yan Chen Xiaodi Wang Bin Wei Yanlin Wang Jun Chen Dongfeng
Department of Gastroenterology, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing, 400042; Center for Cadres Healthcare, People’s Hospital of Xinjiang Uygur Autonomous Region, Urumqi, Xinjiang Uygur Autonomous Region, 830000, China
关键词:
非酒精性脂肪性肝病内质网应激PACS-2GRP78 BaxCaspase-3
Keywords:
non-alcoholic fatty liver disease endoplasmic reticulum stress PACS-2 Bax Caspase-3
分类号:
R-332; R394.2; R575.5
文献标志码:
A
摘要:
目的      探讨PACS-2(phosphofurin acidic cluster sorting protein-2)及其所调控的葡糖调节蛋白78(glucose regulating protein,GRP78)和细胞凋亡标志蛋白Bax、Caspase-3在非酒精性脂肪性肝病(non-alcoholic fatty liver disease, NAFLD)中的表达变化及意义。      方法       应用软脂酸诱导HepG2细胞脂肪变建立非酒精性脂肪性肝病体外模型,并按0、4、8、12、24 h时相点收获细胞,通过油红O(Oil red)染色检测细胞脂肪变程度。同时应用高脂饮食喂SD大鼠建立NAFLD模型,并按时相点分为4、8、12、16、20周组,以普通饮食喂养为对照组。通过q-PCR及Western blot检测PACS-2及内质网应激标志蛋白GRP78和Bax、Caspase-3的表达。      结果       软脂酸成功诱导HepG2细胞脂肪变性,应用高脂饮食喂养SD大鼠成功建立NAFLD大鼠模型。与对照组相比,PACS-2 mRNA相对表达量在HepG2细胞脂肪变模型早期(4、8 h)下降,脂肪变模型晚期(12、24 h)升高; GRP78在8 h组开始上升后,24 h组达到高峰(P<0.01);Bax、Caspase-3的表达均在12、24 h 组显著上升(P<0.01)。在蛋白水平上, PACS-2、GRP78、Bax、Caspase-3的表达与mRNA水平表达基本一致(P<0.01)。NAFLD大鼠模型蛋白表达上, 与对照组相比,PACS-2同样在早期(4、8周)下降,晚期(16、20周)上升(P<0.01);GRP78在表达在4周上调后,20周达到高峰(P<0.01)。Bax、Caspase-3的表达均在晚期显著上升(P<0.01)。      结论       PACS-2早期的低表达可能参与了NAFLD过程中的内质网应激,晚期升高可能与肝细胞凋亡所致的肝损伤密切相关。
Abstract:
Objective       To clarify the expression change and significance of phosphofurin acidic cluster sorting protein-2 (PACS-2) in non-alcoholic fatty liver disease (NAFLD).       Methods       An in vitro NAFLD model was established by inducing the steatosis of HepG2 cells using palmitic acid. The cells were collected at the time points of 0, 4, 8, 12, and 24 h after induction. The steatosis levels were measured by oil red staining. Rat NAFLD model was established in SD rats by feeding high fat diet, while the rats fed with normal food were set as control group. These rats were killed at 4, 8, 12, 16 and 20 weeks after feeding. The expression of PACS-2, endoplasmic reticulum stress marker-glucose regulating protein 78 (GRP78), Bax and Caspase-3 in the cell model and liver tissue samples were detected by q-PCR and Western blotting.       Results      The steatosis of HepG2 cells was induced by fatty acid successfully. The rat NAFLD model was established in SD rats successfully. The relative expression of PACS-2 at mRNA level was significantly decreased in the early stages (4 and 8 h), but increased in the late stages (12 and 24 h after treatment). That of GRP78 was up-regulated in 8 h, and then reached the highest level in 24 h after induction (P<0.01). That of Bax and Caspase-3 was also significantly increased in 12 and 24 h (P<0.01). The expression of these proteins showed similar trends as those at mRNA level (P<0.01). In the rat NAFLD model, the expression of PACS-2 protein was significantly decreased in the early stages (4 and 8 weeks), but then up-regulated in the late stages (16 and 20 weeks, P<0.01). The expression of GRP78 was up-regulated in 4 weeks, and reached the summit in 20 weeks (P<0.01). The expression of Bax and Caspase-3 were significantly up-regulated as compared the control in the late stage of NAFLD(P<0.01).       Conclusion      Mild expression of PACS-2 in the early stage of NAFLD might be involved in endoplasmic reticulum stress during the NAFLD process, and its up-regulation in the late stage may be associated with the apoptosis induced hepatocyte injury.

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更新日期/Last Update: 2013-04-07