Perfusion of medium with supplemented growth factors changes metabolic activities and cell morphology of hepatocyte-nonparenchymal cell coculture
被引:17
作者:
Kan, P
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机构:
Univ Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, JapanUniv Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, Japan
Kan, P
[1
]
Miyoshi, H
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机构:
Univ Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, JapanUniv Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, Japan
Miyoshi, H
[1
]
Ohshima, N
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机构:
Univ Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, JapanUniv Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, Japan
Ohshima, N
[1
]
机构:
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Biomed Engn, Tsukuba, Ibaraki 3058575, Japan
来源:
TISSUE ENGINEERING
|
2004年
/
10卷
/
9-10期
关键词:
D O I:
10.1089/1076327042500346
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
To develop a feasible perfusion-type bioartificial liver device, perfusion of hepatocyte - nonparenchymal cell (NPC) cocultures with medium supplemented with hepatocyte growth factor (HGF) and heparin-binding epidermal growth factor-like growth factor (HB-EGF) was carried out. On day 1 of culture, perfusion at a constant shear stress of 1.3 dyn/cm(2) enhanced ammonia metabolic and urea synthetic activities of hepatocytes. These enhanced activities were sustained up to day 7 only when growth factors were present. In contrast, no beneficial effects of growth factors on these activities were observed in static cultures. In perfusion cultures, three-dimensional cell aggregates were formed. On the surface of these aggregates, flattened cell layers composed mainly of NPCs were found, and the central cluster of cell aggregates was composed of round-shaped hepatocytes and reticulin fibrils. These observations strongly suggested that the reconstruction of different types of liver cells and connective tissues formed tissue-mimicking cell aggregates in the perfusion culture that was able to modulate the liver-specific functions of hepatocytes. Thus, perfusion culture conditions of the hepatocyte - NPC coculture system should be appropriately designed to induce suitable reconstruction of the cultured cells for use as a bioartificial liver device.