Hepatocyte growth factor in physiology and infectious diseases

被引:63
作者
Imamura, Ryu [1 ]
Matsumoto, Kunio [1 ]
机构
[1] Kanazawa Univ, Div Tumor Dynam & Regulat, Canc Res Inst, Kakuma Machi, Kanazawa, Ishikawa 9201192, Japan
基金
日本学术振兴会;
关键词
HGF; Met; Regeneration; Infectious diseases; Hepatocyte growth factor; RECEPTOR TYROSINE KINASE; HELICOBACTER-PYLORI CAGA; C-MET RECEPTOR; GASTRIC EPITHELIAL-CELLS; IN-VITRO; LISTERIA-MONOCYTOGENES; MOLECULAR-CLONING; FACTOR HGF; LIVER-REGENERATION; SIGNALING PATHWAY;
D O I
10.1016/j.cyto.2016.12.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatocyte growth factor (HGF) is a pleiotropic cytokine composed of an alpha-chain and a beta-chain, and these chains contain four kringle domains and a serine protease-like structure, respectively. The receptor for HGF was identified as the c-met proto-oncogene product of transmembrane receptor tyrosine kinase. HGF-induced signaling through the receptor Met provokes dynamic biological responses that support morphogenesis, regeneration, and the survival of various cells and tissues, which includes hepatocytes, renal tubular cells, and neurons. Characterization of tissue-specific Met knockout mice has further indicated that the HGF-Met system modulates immune cell functions and also plays an inhibitory role in the progression of chronic inflammation and fibrosis. However, the biological actions that are driven by the HGF-Met pathway all play a role in the acquisition of the malignant characteristics in tumor cells, such as invasion, metastasis, and drug resistance in the tumor microenvironment. Even though oncogenic Met signaling remains the major research focus, the HGF-Met axis has also been implicated in infectious diseases. Many pathogens try to utilize host HGF-Met system to establish comfortable environment for infection. Their strategies are not only simply change the expression level of HGF or Met, but also actively hijack HGF-Met system and deregulating Met signaling using their pathogenic factors. Consequently, the monitoring of HGF and Met expression, along with real-time detection of Met activation, can be a beneficial biomarker of these infectious diseases. Preclinical studies designed to address the therapeutic significance of HGF have been performed on injury/disease models, including acute tissue injury, chronic fibrosis, and cardiovascular and neurodegenerative diseases. Likewise, manipulating the HGF-Met system with complete control will lead to a tailor made treatment for those infectious diseases. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 117 条
[51]   Human listeriosis and animal models [J].
Lecuit, Marc .
MICROBES AND INFECTION, 2007, 9 (10) :1216-1225
[52]   Activation of hepatocyte growth factor and urokinase/plasminogen activator by matriptase, an epithelial membrane serine protease [J].
Lee, SL ;
Dickson, RB ;
Lin, CY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :36720-36725
[53]   HGF/MET signalling protects Plasmodium-infected host cells from apoptosis [J].
Leiriao, P ;
Albuquerque, SS ;
Corso, S ;
van Gemert, GJ ;
Sauerwein, RW ;
Rodriguez, A ;
Giordano, S ;
Mota, MM .
CELLULAR MICROBIOLOGY, 2005, 7 (04) :603-609
[54]   Hepatocyte growth factor promotes renal epithelial cell survival by dual mechanisms [J].
Liu, YH .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (04) :F624-F633
[55]   Hepatocyte growth factor scatter factor binds with high affinity to dermatan sulfate [J].
Lyon, M ;
Deakin, JA ;
Rahmoune, H ;
Fernig, DG ;
Nakamura, T ;
Gallagher, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :271-278
[56]   Deletion of the Met receptor in the collecting duct decreases renal repair following ureteral obstruction [J].
Ma, Hong ;
Saenko, Maryanna ;
Opuko, Anthony ;
Togawa, Akashi ;
Soda, Keita ;
Marlier, Arnaud ;
Moeckel, Gilbert W. ;
Cantley, Lloyd G. ;
Ishibe, Shuta .
KIDNEY INTERNATIONAL, 2009, 76 (08) :868-876
[57]   Novel Death Defying Domain in Met Entraps the Active Site of Caspase-3 and Blocks Apoptosis in Hepatocytes [J].
Ma, Jihong ;
Zou, Chunbin ;
Guo, Lida ;
Seneviratne, Danushka S. ;
Tan, Xinping ;
Kwon, Yong-Kook ;
An, Jiyan ;
Bowser, Robert ;
DeFrances, Marie C. ;
Zarnegar, Reza .
HEPATOLOGY, 2014, 59 (05) :2010-2021
[58]   Loss of c-Met accelerates development of liver fibrosis in response to CCl4 exposure through deregulation of multiple molecular pathways [J].
Marquardt, Jens U. ;
Seo, Daekwan ;
Gomez-Quiroz, Luis E. ;
Uchida, Koichi ;
Gillen, Matthew C. ;
Kitade, Mitsuteru ;
Kaposi-Novak, Pal ;
Conner, Elizabeth A. ;
Factor, Valentina M. ;
Thorgeirsson, Snorri S. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2012, 1822 (06) :942-951
[59]   GENETIC DISRUPTION OF MET SIGNALING IMPAIRS GABAergic STRIATAL DEVELOPMENT AND COGNITION [J].
Martins, G. J. ;
Shahrokh, M. ;
Powell, E. M. .
NEUROSCIENCE, 2011, 176 :199-209
[60]  
Matsumoto K, 1996, J BIOCHEM-TOKYO, V119, P591