Cellular Mechanisms of Tissue Fibrosis. 5. Novel insights into liver fibrosis

被引:275
作者
Mallat, Ariane [1 ,2 ,3 ]
Lotersztajn, Sophie [1 ,2 ,3 ]
机构
[1] Hop Henri Mondor, INSERM, U955, F-94010 Creteil, France
[2] Univ Paris Est, UMR S955, Creteil, France
[3] Hop H Mondor Albert Chenevier, AP HP, Serv Hepatol & Gastroenterol, Creteil, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2013年 / 305卷 / 08期
关键词
myofibroblasts; hepatic stellate cells; inflammation; chronic liver disease; HEPATIC STELLATE CELLS; GROWTH-FACTOR; NATURAL-KILLER; CB1; RECEPTORS; RISK-FACTOR; T-CELLS; INJURY; DIFFERENTIATION; FIBROGENESIS; PROGRESSION;
D O I
10.1152/ajpcell.00230.2013
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Liver fibrosis is the common scarring reaction associated with chronic liver injury that results from prolonged parenchymal cell injury and/or inflammation. The fibrogenic response is characterized by progressive accumulation of extracellular matrix components enriched in fibrillar collagens and a failure of matrix turnover. This process is driven by a heterogeneous population of hepatic myofibroblasts, which mainly derive from hepatic stellate cells and portal fibroblasts. Regression of fibrosis can be achieved by the successful control of chronic liver injury, owing to termination of the fibrogenic reaction following clearance of hepatic myofibroblasts and restoration of fibrolytic pathways. Understanding of the complex network underlying liver fibrogenesis has allowed the identification of a large number of antifibrotic targets, but no antifibrotic drug has as yet been approved. This review will highlight recent advances regarding the mechanisms that regulate liver fibrogenesis and fibrosis regression, with special focus on novel signaling pathways and the role of inflammatory cells. Translation of these findings to therapies will require continued efforts to develop multitarget therapeutic approaches that will improve the grim prognosis of liver cirrhosis.
引用
收藏
页码:C789 / C799
页数:11
相关论文
共 99 条
[1]
PPARα Expression Protects Male Mice from High Fat-Induced Nonalcoholic Fatty Liver [J].
Abdelmegeed, Mohamed A. ;
Yoo, Seong-Ho ;
Henderson, Lauren E. ;
Gonzalez, Frank J. ;
Woodcroft, Kimberley J. ;
Song, Byoung-Joon .
JOURNAL OF NUTRITION, 2011, 141 (04) :603-610
[2]
Inhibition of hepatocyte autophagy increases tumor necrosis factor-dependent liver injury by promoting caspase-8 activation [J].
Amir, M. ;
Zhao, E. ;
Fontana, L. ;
Rosenberg, H. ;
Tanaka, K. ;
Gao, G. ;
Czaja, M. J. .
CELL DEATH AND DIFFERENTIATION, 2013, 20 (07) :878-887
[3]
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
[4]
Allosteric inhibition of lysyl oxidase-like-2 impedes the development of a pathologic microenvironment [J].
Barry-Hamilton, Vivian ;
Spangler, Rhyannon ;
Marshall, Derek ;
McCauley, Scott ;
Rodriguez, Hector M. ;
Oyasu, Miho ;
Mikels, Amanda ;
Vaysberg, Maria ;
Ghermazien, Haben ;
Wai, Carol ;
Garcia, Carlos A. ;
Velayo, Arleene C. ;
Jorgensen, Brett ;
Biermann, Donna ;
Tsai, Daniel ;
Green, Jennifer ;
Zaffryar-Eilot, Shelly ;
Holzer, Alison ;
Ogg, Scott ;
Thai, Dung ;
Neufeld, Gera ;
Van Vlasselaer, Peter ;
Smith, Victoria .
NATURE MEDICINE, 2010, 16 (09) :1009-U107
[5]
Distinct proteomic features of two fibrogenic liver cell populations: Hepatic stellate cells and portal myofibroblasts [J].
Bosselut, Nelly ;
Housset, Chantal ;
Marcelo, Paulo ;
Rey, Colette ;
Burmester, Thorsten ;
Vinh, Joeelle ;
Vaubourdolle, Michel ;
Cadoret, Axelle ;
Baudin, Bruno .
PROTEOMICS, 2010, 10 (05) :1017-1028
[6]
Macrophage-derived Wnt opposes Notch signaling to specify hepatic progenitor cell fate in chronic liver disease [J].
Boulter, Luke ;
Govaere, Olivier ;
Bird, Tom G. ;
Radulescu, Sorina ;
Ramachandran, Prakash ;
Pellicoro, Antonella ;
Ridgway, Rachel A. ;
Seo, Sang Soo ;
Spee, Bart ;
Van Rooijen, Nico ;
Sansom, Owen J. ;
Iredale, John P. ;
Lowell, Sally ;
Roskams, Tania ;
Forbes, Stuart J. .
NATURE MEDICINE, 2012, 18 (04) :572-579
[7]
Long-Term Entecavir Therapy Results in the Reversal of Fibrosis/Cirrhosis and Continued Histological Improvement in Patients with Chronic Hepatitis B [J].
Chang, Ting-Tsung ;
Liaw, Yun-Fan ;
Wu, Shun-Sheng ;
Schiff, Eugene ;
Han, Kwang-Hyub ;
Lai, Ching-Lung ;
Safadi, Rifaat ;
Lee, Samuel S. ;
Halota, Waldemar ;
Goodman, Zachary ;
Chi, Yun-Chan ;
Zhang, Hui ;
Hindes, Robert ;
Iloeje, Uchenna ;
Beebe, Suzanne ;
Kreter, Bruce .
HEPATOLOGY, 2010, 52 (03) :886-893
[8]
Liver fatty acid binding protein (L-Fabp) modulates murine stellate cell activation and diet-induced nonalcoholic fatty liver disease [J].
Chen, Anping ;
Tang, Youcai ;
Davis, Victoria ;
Hsu, Fong-Fu ;
Kennedy, Susan M. ;
Song, Haowei ;
Turk, John ;
Brunt, Elizabeth M. ;
Newberry, Elizabeth P. ;
Davidson, Nicholas O. .
HEPATOLOGY, 2013, 57 (06) :2202-2212
[9]
Hedgehog Controls Hepatic Stellate Cell Fate by Regulating Metabolism [J].
Chen, Yuping ;
Choi, Steve S. ;
Michelotti, Gregory A. ;
Chan, Isaac S. ;
Swiderska-Syn, Marzena ;
Karaca, Gamze F. ;
Xie, Guanhua ;
Moylan, Cynthia A. ;
Garibaldi, Francesca ;
Premont, Richard ;
Suliman, Hagir B. ;
Piantadosi, Claude A. ;
Diehl, Anna Mae .
GASTROENTEROLOGY, 2012, 143 (05) :1319-+
[10]
C-C Motif Chemokine Receptor 9 Positive Macrophages Activate Hepatic Stellate Cells and Promote Liver Fibrosis in Mice [J].
Chu, Po-sung ;
Nakamoto, Nobuhiro ;
Ebinuma, Hirotoshi ;
Usui, Shingo ;
Saeki, Keita ;
Matsumoto, Atsuhiro ;
Mikami, Yohei ;
Sugiyama, Kazuo ;
Tomita, Kengo ;
Kanai, Takanori ;
Saito, Hidetsugu ;
Hibi, Toshifumi .
HEPATOLOGY, 2013, 58 (01) :337-350