Hepatic Stellate Cell and Myofibroblast-Like Cell Gene Expression in the Explanted Cirrhotic Livers of Patients Undergoing Liver Transplantation

被引:4
作者
Estep, J. Michael [1 ,2 ]
O'Reilly, Linda [3 ]
Grant, Geraldine [3 ]
Piper, James [1 ]
Jonsson, Johann [1 ]
Afendy, Arian [1 ,2 ]
Chandhoke, Vikas [3 ]
Younossi, Zobair M. [1 ,2 ,3 ]
机构
[1] Inova Fairfax Hosp, Ctr Liver Dis, Falls Church, VA 22042 USA
[2] Inova Hlth Syst, Translat Res Inst, Falls Church, VA USA
[3] George Mason Univ, Mol & Microbiol Dept, Ctr Study Genom Liver Dis, Fairfax, VA 22030 USA
关键词
Cirrhosis; Stellate cells; Inflammation; Gene expression; Myofibroblast-like cell; FIBROSIS; MECHANISMS; MEDICINE; INJURY;
D O I
10.1007/s10620-009-0919-9
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Hepatic stellate cells (HSC) are involved in hepatic fibrogenesis. Cell signaling associated with an insult to the liver affects an HSC transdifferentiation to fibrogenic myofibroblast-like cells. Aims To investigate the transcriptional expression distinguishing HSC and myofibroblast-like cells between livers with and without cirrhosis. Methods Tissue from ten cirrhotic livers (undergoing transplant) and four non-cirrhotic livers from the National Disease Research Interchange underwent cell separation to extract HSC and myofibroblast-like cell populations. Separated cell types as well as LI-90 cells were subjected to microarray analysis. Selected microarray results were verified by quantitative real-time PCR. Results Differential expression of some genes, such as IL-1 beta, IL-1 alpha, and IL-6, was associated with both transdifferentiation and disease. Other genes, such as fatty acid 2-hydroxylase only show differential expression in association with disease. Functional analysis supported these findings, indicating some signal transduction pathways (IL-6) are involved in disease and activation, whereas retinoid X receptor signaling in HSC from cirrhotic and non-cirrhotic livers varies in scope and quality. Conclusions These findings indicate distinct phenotypes for HSC from cirrhotic and non-cirrhotic livers. Furthermore, coordinated differential expression between genes involved in the same signal transduction pathways provides some insight into the mechanisms that may control the balance between fibrogenesis and fibrolysis.
引用
收藏
页码:496 / 504
页数:9
相关论文
共 12 条
[1]   Hepatic stellate cell lipid droplets: A specialized lipid droplet for retinoid storage [J].
Blaner, William S. ;
O'Byrne, Sheila M. ;
Wongsiriroj, Nuttaporn ;
Kluwe, Johannes ;
D'Ambrosio, Diana M. ;
Jiang, Hongfeng ;
Schwabe, Robert F. ;
Hillman, Elizabeth M. C. ;
Piantedosi, Roseann ;
Libien, Jenny .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2009, 1791 (06) :467-473
[2]   Hepatic fibrosis-Overview [J].
Friedman, Scott L. .
TOXICOLOGY, 2008, 254 (03) :120-129
[3]  
FRIEDMAN SL, 1993, NEW ENGL J MED, V328, P1828
[4]   Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury [J].
Friedman, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (04) :2247-2250
[5]   History, heterogeneity, developmental biology, and functions of quiescent hepatic stellate cells [J].
Geerts, A .
SEMINARS IN LIVER DISEASE, 2001, 21 (03) :311-335
[6]   Development of a new reference standard for microarray experiments [J].
Gorreta, F ;
Barzaghi, D ;
VanMeter, AJ ;
Chandhoke, V ;
Del Giacco, L .
BIOTECHNIQUES, 2004, 36 (06) :1002-+
[7]   Science, medicine, and the future - Cirrhosis: new research provides a basis for rational and targeted treatments [J].
Iredale, JP .
BMJ-BRITISH MEDICAL JOURNAL, 2003, 327 (7407) :143-147
[8]   Apoptosis of hepatic stellate cells: involvement in resolution of biliary fibrosis and regulation by soluble growth factors [J].
Issa, R ;
Williams, E ;
Trim, N ;
Kendall, T ;
Arthur, MJP ;
Reichen, J ;
Benyon, RC ;
Iredale, JP .
GUT, 2001, 48 (04) :548-557
[9]   Mechanisms of Disease Progression in Nonalcoholic Fatty Liver Disease [J].
Jou, Janice ;
Choi, Steve S. ;
Diehl, Anna Mae .
SEMINARS IN LIVER DISEASE, 2008, 28 (04) :370-379
[10]   Early genes induced in hepatic stellate cells during wound healing [J].
Lalazar, A ;
Wong, L ;
Yamasaki, G ;
Friedman, SL .
GENE, 1997, 195 (02) :235-243