A Nanofiber Membrane Maintains the Quiescent Phenotype of Hepatic Stellate Cells

被引:4
作者
Eda, Hiroyuki [1 ,2 ]
Kulig, Katherine M. [3 ]
Steiner, Toni A. [2 ]
Shimada, Hideaki [2 ]
Patel, Krupali [2 ]
Park, Eric [4 ]
Kim, Ernest S. [5 ]
Borenstein, Jeffrey T. [5 ]
Neville, Craig M. [3 ]
Keller, Bradley T. [2 ]
机构
[1] Ajinomoto Pharmaceut Co Ltd, Exploratory Res Labs, Kawasaki, Kanagawa, Japan
[2] Pfizer Inc, Pfizer Global Res & Dev, St Louis Labs, Discovery Biol, Chesterfield, MO USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Regenerat Med, Boston, MA USA
[4] Pfizer Inc, Pfizer Global Res & Dev, Res Technol Ctr, Cambridge, MA USA
[5] Charles Stark Draper Lab Inc, Cambridge, MA 02139 USA
关键词
Hepatic stellate cell; Nanofiber membrane; Stress fiber; Growth factor; Quiescent; MESENCHYMAL STEM-CELLS; PEPTIDE-AMPHIPHILE NANOFIBERS; EXTRACELLULAR-MATRIX; LIVER MYOFIBROBLASTS; ROCK INHIBITOR; TGF-BETA; COLLAGEN; RAT; GROWTH; ACTIVATION;
D O I
10.1007/s10620-012-2084-9
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatic stellate cells (HSC) play a major role in the progression of liver fibrosis. The aim of our study was to investigate whether rat HSC cultured on a nanofiber membrane (NM) retain their quiescent phenotype during both short- and long-term culture and whether activated HSC revert to a quiescent form when re-cultured on NM. Rat HSC cultured for 1 day on plastic plates (PP) were used as quiescent HSC, while cells cultured for 1 week on PP were considered to be activated HSC. Quiescent or activated HSC were subsequently plated on PP or NM and cultured for an additional 4 days at which time their gene expression, stress fiber development, and growth factor production were determined. For long-term culture, HSC were grown on NM for 20 days and the cells then replated on PP and cultured for another 10 days. Expression of marker genes for HSC activation, stress fiber development, and growth factor production were significantly lower in both quiescent and activated HSC cultured on NM than in those cultured on PP. After long-term culture on NM, activation marker gene expression and stress fiber development were still significantly lower in HSC than in PP, and HSC still retained the ability to activate when replated onto PP. HSC cultured on NM retained quiescent characteristics after both short- and long-term culture while activated HSC reverted toward a quiescent state when cultured on NM. Cultures of HSC grown on NM are a useful in vitro model to investigate the mechanisms of activation and deactivation.
引用
收藏
页码:1152 / 1162
页数:11
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