Maintenance of integrity and function of isolated hepatocytes during extended suspension culture at 25°C

被引:12
作者
Wigg, AJ [1 ]
Phillips, JW
Berry, MN
机构
[1] Flinders Med Ctr, Dept Gastroenterol & Hepatol, Bedford Pk, SA 5042, Australia
[2] Flinders Med Ctr, Dept Med Biochem, Bedford Pk, SA 5042, Australia
[3] Flinders Univ S Australia, Dept Med Biochem, Adelaide, SA 5001, Australia
[4] Flinders Univ S Australia, Dept Human Physiol, Adelaide, SA 5001, Australia
关键词
bioartificial liver; hypothermia; metabolism; albumin synthesis; transmission electron microscopy; isolated hepatocytes; suspension culture;
D O I
10.1034/j.1600-0676.2003.00817.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Isolated hepatocytes in suspension provide a number of advantages for use in bioartificial liver device, however, poor stability of this cell preparation at physiological temperatures is an apparent barrier preventing their use. We therefore investigated the integrity and differentiated function of isolated rat hepatocytes under conditions of mild hypothermia. Isolated hepatocytes were suspended in a bicarbonate buffered saline medium, supplemented with glucose and bovine serum albumin (BSA), and maintained for 48 h at 25degreesC on a rotary shaker under an atmosphere of 95% O-2 and 5% CO2. Under these conditions there was no significant decline in cell viability and good preservation of cellular morphology on transmission electron microscopy for at least 24 h. Isolated hepatocytes in suspension at 25degreesC were also able to maintain normal Na+ and K+ ion gradients. The cellular energy status ([ATP], ATP/ADP ratio, cytoplasmic and mitochondrial redox potentials), metabolic function (urea synthesis and ammonia removal), albumin synthesis and phase I and phase II drug detoxification activity of these cells were also maintained for at least 24 h post isolation. These observations demonstrate the robust nature of mildly hypothermic isolated hepatocytes in suspension and encourage further studies re-examining the feasibility of using this cell preparation in bioartificial livers.
引用
收藏
页码:201 / 211
页数:11
相关论文
共 37 条
[1]   Advances in bioartificial liver devices [J].
Allen, JW ;
Hassanein, T ;
Bhatia, SN .
HEPATOLOGY, 2001, 34 (03) :447-455
[2]  
BERGMEYER HU, 1974, METHODS ENZYMATIC AN
[3]  
Berry M.N., 1991, ISOLATED HEPATOCYTES, P15, DOI DOI 10.1016/S0075-7535(08)70023-8
[4]   INTRACELLULAR MITOCHONDRIAL-MEMBRANE POTENTIAL AS AN INDICATOR OF HEPATOCYTE ENERGY-METABOLISM - FURTHER EVIDENCE FOR THERMODYNAMIC CONTROL OF METABOLISM [J].
BERRY, MN ;
GREGORY, RB ;
GRIVELL, AR ;
HENLY, DC ;
NOBES, CD ;
PHILLIPS, JW ;
WALLACE, PG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 936 (03) :294-306
[5]   HIGH-YIELD PREPARATION OF ISOLATED RAT LIVER PARENCHYMAL CELLS - A BIOCHEMICAL AND FINE STRUCTURAL STUDY [J].
BERRY, MN ;
FRIEND, DS .
JOURNAL OF CELL BIOLOGY, 1969, 43 (03) :506-+
[6]  
BERRY MN, 1997, BIOARTIFICIAL LIVER, P70
[7]   EFFECTS OF SERIAL RESIN HEMOPERFUSION IN FULMINANT HEPATIC-FAILURE [J].
BIHARI, D ;
HUGHES, RD ;
GIMSON, AES ;
LANGLEY, PG ;
EDE, RJ ;
EDER, G ;
WILLIAMS, R .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1983, 6 (06) :299-302
[8]   Effects of hypothermia on hypoxia-induced apoptosis in cultured neurons from developing rat forebrain:: Comparison with preconditioning [J].
Bossenmeyer-Pourié, C ;
Koziel, V ;
Daval, JL .
PEDIATRIC RESEARCH, 2000, 47 (03) :385-391
[9]  
CHEN RF, 1967, J BIOL CHEM, V242, P173
[10]  
DEBARTOLO L, 2000, HEPATOCYTE REV, P585