中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

巨噬细胞在非酒精性脂肪性肝病中的作用

罗雨欣 郭金波 张晓岚

引用本文:
Citation:

巨噬细胞在非酒精性脂肪性肝病中的作用

DOI: 10.3969/j.issn.1001-5256.2020.03.046
基金项目: 

国家自然科学基金资助项目(81900522); 

详细信息
  • 中图分类号: R575.5

Research advances in the role of macrophages in nonalcoholic fatty liver disease

Research funding: 

 

  • 摘要: 随着生活水平的提高,非酒精性脂肪性肝病(NAFLD)发病率逐年升高并且趋于年轻化,但其具体发病机制尚未明确。巨噬细胞作为参与NAFLD发病的重要细胞之一,一直广受关注。针对肝脏巨噬细胞的来源及分类、巨噬细胞在NAFLD肝脏炎症中的作用和其活化的机制、靶向巨噬细胞药物进行阐述,旨在为临床治疗NAFLD提供参考。

     

  • [1] YOUNOSSI ZM,MARCHESINI G,PINTO-CORTEZ H,et al.Epidemiology of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis:Implications for liver transplantation[J].Transplantation,2019,103(1):22-27.
    [2] YOUNOSSI Z,TACKE F,ARRESE M,et al. Global perspectives on non-alcoholic fatty liver disease and non-alcoholic steatohepatitis[J]. Hepatology,2019,69(6):2672-2682.
    [3] ZHU JZ,ZHOU QY,WANG YM,et al. Prevalence of fatty liver disease and the economy in China:A systematic review[J].World J Gastroenterol,2015,21(18):5695-5706.
    [4] BIJNEN M,JOSEFS T,CUIJPERS I,et al. Adipose tissue macrophages induce hepatic neutrophil recruitment and macrophage accumulation in mile[J]. Gut,2018,67(7):1317-1327.
    [5] MRIDHA AR,WREE A,AAB R,et al. NLRP3 inflammasome blockade reduces liver inflammation and fibrosis in experimental NASH in mice[J]. J Hepatol,2017,66(5):1037-1046.
    [6] IMAJO K,FUJITA K,YONEDA M,et al. Hyperresponsivity to low-dose endotoxin during progression to nonalcoholic steatohepatitis is regulated by leptin-mediated signaling[J].Cell Metab,2012,16(1):44-54.
    [7] YAMADA S,KAMADA N,AMIYA T,et al. Gut microbiotamediated generation of saturated fatty acids elicits inflammation in the liver in murine high-fat diet-induced steatohepatitis[J]. BMC Gastroenterol,2017,17(1):136.
    [8] GADD VL,SKOIEN R,POWELL EE,et al. The portal inflammatory infiltrate and ductular reaction in human nonalcoholic fatty liver disease[J]. Hepatology,2014,59(4):1393-1405.
    [9] PARK JW,JEONG G,KIM SJ,et al. Predictors reflecting the pathological severity of non-alcoholic fatty liver disease:Comprehensive study of clinical and immunohistochemical findings in younger Asian patients[J]. J Gastroenterol Hepatol,2007,22(4):491-497.
    [10] TOSELLO-TRAMPONT AC,LANDES SG,NGUYEN V,et al.Kuppfer cells trigger nonalcoholic steatohepatitis development in diet-induced mouse model through tumor necrosis factor-αproduction[J]. J Biol Chem,2012,287(48):40161-40172.
    [11] SONG M,SCHUSCHKE DA,ZHOU Z,et al. Kupffer cell depletion protects against the steatosis,but not the liver damage,induced by marginal-copper,high-fructose diet in male rats[J]. Am J Physiol Gastrointest Liver Physiol,2015,308(11):g934-g945.
    [12] RENSEN SS,SLAATS Y,NIJHUIS J,et al. Increased hepatic myeloperoxidase activity in obese subjects with nonalcoholic steatohepatitis[J]. Am J Pathol,2009,175(4):1473-1482.
    [13] JINDAL A,BRUZZI S,SUTTI S,et al. Fat-laden macrophages modulate lobular inflammation in nonalcoholic steatohepatitis(NASH)[J]. Exp Mol Pathol,2015,99(1):155-162.
    [14] STANTON MC,CHEN SC,JACKSON JV,et al. Inflammatory signals shift from adipose to liver during high fat feeding and influence the development of steatohepatitis in mice[J]. J Inflamm(Lond),2011,8:8.
    [15] du PLESSIS J,van PELT J,KORF H,et al. Association of adipose tissue inflammation with histological severity of nonalcoholic fatty liver disease[J]. Gastroenterology,2015,149(3):635-648,e14.
    [16] WREE A,EGUCHI A,MCGEOUGH MD,et al. NLRP3 inflammasome activation results in hepatocyte pyroptosis,liver inflammation,and fibrosis in mice[J]. Hepatology,2014,59(3):898-910.
    [17] GONG Z,ZHOU J,ZHAO S,et al. Chenodeoxycholic acid activates NLRP3 inflammasome and contributes to cholestatic liver fibrosis[J]. Oncotarget,2016,7(51):83951-83963.
    [18] BÄCKHED F,DING H,WANG T,et al. The gut microbiota as an environmental factor that regulates fat storage[J]. Proc Natl Acad Sci U S A,2004,101(44):15718-15723.
    [19] YE JZ,LI YT,WU WR,et al. Dynamic alterations in the gut microbiota and metabolome during the development of methionine-choline-defcient diet-induced nonalcoholic steatohepatitis[J]. World J Gastroenterol,2018,24(23):2468-2481.
    [20] ROBERT O,BOUJEDIDI H,BIGORGNE A,et al. Decreased expression of the glucocorticoid receptor-GILZ pathway in Kupffer cells promotes liver inflammation in obese mice[J]. J Hepatol,2016,64(4):916-924.
    [21] SVENDSEN P,GRAVERSEN JH,ETZERODT A,et al. Antibody-directed glucocorticoid targeting to CD163 in M2-type macrophages attenuates fructose-induced liver inflammatory changes[J]. Mol Ther Methods Clin Dev,2017,4:50-61.
    [22] LEFEBVRE E,MOYLE G,RESHEF R,et al. Antifibrotic effects of the dual CCR2/CCR5 antagonist cenicriviroc in animal models of liver and kidney fibrosis[J]. PLo S One,2016,11(6):e0158156.
    [23] KRENKEL O,PUENGEL T,GOVAERE O,et al. Therapeutic inhibition of inflammatory monocyte recruitment reduces steatohepatitis and liver fibrosis[J]. Hepatology,2018,67(4):1270-1283.
    [24] FRIEDMAN SL,RATZIU V,HARRISON SA,et al. A randomized,placebo-controlled trial of cenicriviroc for treatment of nonalcoholic steatohepatitis with fibrosis[J]. Hepatology,2018,67(5):1754-1767.
    [25] IACOBINI C,MENINI S,RICCI C,et al. Galectin-3 ablation protects mice from diet-induced NASH:A major scavenging role for galectin-3 in liver[J]. J Hepatol,2011,54(5):975-983.
    [26] NOMOTO K,NISHIDA T,NAKANISHI Y,et al. Deficiency in galectin-3 promotes hepatic injury in CDAA diet-induced nonalcoholic fatty liver disease[J]. Sci World J,2012,2012:959824.
    [27] JEFTIC I,JOVICIC N,PANTIC J,et al. Galectin-3 ablation enhances liver steatosis,but attenuates inflammation and IL-33-dependent fibrosis in obesogenic mouse model of nonalcoholic steatohepatitis[J]. Mol Med,2015,21:453-465.
    [28] TRRABER PG,ZOMER E. Therapy of experimental NASH and fibrosis with galectin inhibitors[J]. PLo S One,2013,8(12):e83481.
    [29] HARRISON SA,MARRI SR,CHALASANI N,et al. Randomised clinical study:GR-MD-02,a galectin-3 inhibitor,vs.placebo in patients having non-alcoholic steatohepatitis with advanced fibrosis[J]. Aliment Pharmacol Ther,2016,44(11-12):1183-1198.
    [30] YAO J,ZHOU CS,MA X,et al. FXR agonist GW4064 alleviates endotoxin-induced hepatic inflammation by repressing macrophage activation[J]. World J Gastroenterol,2014,20(39):14430-14441.
    [31] NEUSCHWANDER-TETRI BA,LOOMBA R,SANYAL AJ,et al.Farnesoid X nuclear receptor ligand obeticholic acid for non-cirrhotic,non-alcoholic steatohepatitis(FLINT):A multicentre,randomised,placebo-controlled trial[J]. Lancet,2015,385(9972):956-965.
    [32] YAMAMOTO T,NAKADE Y,YAMAUCHI T,et al. Glucagonlike peptide-1 analogue prevents nonalcoholic steatohepatitis in non-obese mice[J]. World J Gastroenterol,2016,22(8):2512-2523.
    [33] ARMSTRONG MJ,GAUNT P,AITHAL GP,et al. Liraglutide safety and efficacy in patients with non-alcoholic steatohepatitis(LEAN):A multicentre,double-blind,randomised,placebo-controlled phase 2 study[J]. Lancet,2016,387(10019):679-690.
    [34] ALASFOOR S,ROHM TV,BOSCH AJT,et al. Imatinib reduces non-alcoholic fatty liver disease in obese mice by targeting inflammatory and lipogenic pathways in macrophages and liver[J]. Sci Rep,2018,8(1):15331.
  • 加载中
计量
  • 文章访问数:  963
  • HTML全文浏览量:  35
  • PDF下载量:  243
  • 被引次数: 0
出版历程
  • 收稿日期:  2019-10-17
  • 出版日期:  2020-03-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回