Therapeutic potential of targeting regulatory mechanisms of hepatic stellate cell activation in liver fibrosis

被引:56
作者
Baghaei, Kaveh [1 ,2 ]
Mazhari, Sogol [1 ]
Tokhanbigli, Samaneh [1 ]
Parsamanesh, Gilda [1 ]
Alavifard, Helia [1 ]
Schaafsma, Dedmer [3 ]
Ghavami, Saeid [4 ,5 ,6 ,7 ]
机构
[1] Shahid Beheshti Univ Med Sci, Res Inst Gastroenterol & Liver Dis, Basic & Mol Epidemiol Gastrointestinal Disorders, Tehran 1985717413, Iran
[2] Shahid Beheshti Univ Med Sci, Res Inst Gastroenterol & Liver Dis, Gastroenterol & Liver Dis Res Ctr, Tehran 1985717413, Iran
[3] Sci Impact, Winnipeg, MB, Canada
[4] Univ Manitoba, Rady Fac Hlth Sci, Max Rady Coll Med, Dept Human Anat & Cell Sci, Winnipeg, MB, Canada
[5] Univ Manitoba, Canc Care Manitoba, Res Inst Oncol & Hematol, Winnipeg, MB R3E 0V9, Canada
[6] Univ Manitoba, Children Hosp Res Inst Manitoba, Biol Breathing Theme, Winnipeg, MB R3E 0V9, Canada
[7] Katowice Sch Technol, Fac Med, PL-40555 Katowice, Poland
关键词
Liver diseases; Extracellular signaling; Cell phenotype; Fibrogenic myofibroblasts; Autophagy; NF-KAPPA-B; HEDGEHOG SIGNALING INHIBITOR; TGF-BETA; ANTIFIBROTIC ACTIVITY; EXTRACELLULAR-MATRIX; RECEPTOR; AUTOPHAGY; PATHWAY; ANGIOGENESIS; PDGF;
D O I
10.1016/j.drudis.2021.12.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hepatic fibrosis is a manifestation of different etiologies of liver disease with the involvement of multiple mediators in complex network interactions. Activated hepatic stellate cells (aHSCs) are the central driver of hepatic fibrosis, given their potential to induce connective tissue formation and extracellular matrix (ECM) protein accumulation. Therefore, identifying the cellular and molecular pathways involved in the activation of HSCs is crucial in gaining mechanistic and therapeutic perspectives to more effectively target the disease. In addition to a comprehensive summary of our current understanding of the role of HSCs in liver fibrosis, we also discuss here the proposed therapeutic strategies based on targeting HSCs.
引用
收藏
页码:1044 / 1061
页数:18
相关论文
共 166 条
[1]   Peroxisome Proliferator-Activated Receptor Gamma Agonist Attenuates Liver Fibrosis by Several Fibrogenic Pathways in an Animal Model of Cholestatic Fibrosis [J].
Alatas, Fatima Safira ;
Matsuura, Toshiharu ;
Pudjiadi, Antonius Hocky ;
Wijaya, Stephanie ;
Taguchi, Tomoaki .
PEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION, 2020, 23 (04) :346-355
[2]   CX3CL1-CX3CR1 Interaction Prevents Carbon Tetrachloride-Induced Liver Inflammation and Fibrosis in Mice [J].
Aoyama, Tomonori ;
Inokuchi, Sayaka ;
Brenner, David A. ;
Seki, Ekihiro .
HEPATOLOGY, 2010, 52 (04) :1390-1400
[3]   Burden of liver diseases in the world [J].
Asrani, Sumeet K. ;
Devarbhavi, Harshad ;
Eaton, John ;
Kamath, Patrick S. .
JOURNAL OF HEPATOLOGY, 2019, 70 (01) :151-171
[4]   Antifibrotics in liver disease: are we getting closer to clinical use? [J].
Bansal, Meena B. ;
Chamroonkul, Naichaya .
HEPATOLOGY INTERNATIONAL, 2019, 13 (01) :25-39
[5]   The pan-caspase inhibitor Emricasan (IDN-6556) decreases liver injury and fibrosis in a murine model of non-alcoholic steatohepatitis [J].
Barreyro, Fernando J. ;
Holod, Silvia ;
Finocchietto, Paola V. ;
Camino, Alejandra M. ;
Aquino, Jorge B. ;
Avagnina, Alejandra ;
Carreras, Maria C. ;
Poderoso, Juan J. ;
Gores, Gregory J. .
LIVER INTERNATIONAL, 2015, 35 (03) :953-966
[6]  
Bartneck M, 2020, CELL MOL GASTROENTER
[7]   Serelaxin increases the antifibrotic action of rosiglitazone in a model of hepatic fibrosis [J].
Bennett, Robert G. ;
Simpson, Ronda L. ;
Hamel, Frederick G. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2017, 23 (22) :3999-4006
[8]   Deletion of tumour necrosis factor α receptor 1 elicits an increased TH17 immune response in the chronically inflamed liver [J].
Berkhout, Laura ;
Barikbin, Roja ;
Schiller, Birgit ;
Ravichandran, Gevitha ;
Krech, Till ;
Neumann, Katrin ;
Sass, Gabriele ;
Tiegs, Gisa .
SCIENTIFIC REPORTS, 2019, 9 (1)
[9]   Hepatic acute phase proteins - Regulation by IL-6-and IL-1-type cytokines involving STAT3 and its crosstalk with NF-κB-dependent signaling [J].
Bode, Johannes G. ;
Albrecht, Ute ;
Haeussinger, Dieter ;
Heinrich, Peter C. ;
Schaper, Fred .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2012, 91 (6-7) :496-505
[10]   CX3CL1/fractalkine shedding by human hepatic stellate cells: contribution to chronic inflammation in the liver [J].
Bourd-Boittin, Katia ;
Basset, Laetitia ;
Bonnier, Dominique ;
L'Helgoualc'h, Annie ;
Samson, Michel ;
Theret, Nathalie .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2009, 13 (8A) :1526-1535