-
Something wrong with this record ?
Expression of mRNAs related to connective tissue metabolism in rat hepatic stellate cells and myofibroblasts
Jiroutova A, Slavkovsky R, Cermakova M, Majdiakova L, Hanovcova I, Bolehovska R, Hajzlerova M, Radilova H, Ruszova E, Kanta J.
Language English Country Germany
Document type Comparative Study
- MeSH
- Liver Cirrhosis, Experimental metabolism MeSH
- Gene Expression MeSH
- Extracellular Matrix chemistry MeSH
- Fibroblasts cytology metabolism drug effects MeSH
- Financing, Organized MeSH
- Immunohistochemistry MeSH
- Liver cytology metabolism drug effects MeSH
- Rats MeSH
- Cells, Cultured MeSH
- RNA, Messenger biosynthesis drug effects MeSH
- Metalloproteases genetics metabolism MeSH
- Myocytes, Smooth Muscle cytology metabolism drug effects MeSH
- Carbon Tetrachloride Poisoning MeSH
- Connective Tissue metabolism drug effects MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Proteoglycans genetics metabolism MeSH
- Oligonucleotide Array Sequence Analysis MeSH
- Tissue Inhibitor of Metalloproteinases MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Comparative Study MeSH
Hepatic stellate cells (HSC) and liver myofibroblasts (MFB) are two cell populations most likely responsible for the synthesis of most connective tissue components in fibrotic liver. They differ in their origin and location, and possibly in patterns of gene expression. Normal and carbon tetrachloride-cirrhotic livers from rats were used to isolate HSC. Liver was perfused with pronase and collagenase solutions, followed by centrifugation of the cell suspension on a density gradient. HSC were quiescent 2 days after plating on plastic but they became activated after another 5 days in culture. When the culture was passaged 5 times, its character changed profoundly as HSC were replaced by MFB. Microarray analysis was used to determine gene expression in quiescent HSC, activated HSC and MFB. The expression of 49 genes coding for connective tissue proteins, proteoglycans, metalloproteinases and their inhibitors, growth factors and cellular markers was determined. The pattern of gene expression changed during HSC activation and there were distinct differences between HSC and MFB. Little difference between normal cells and cells isolated from cirrhotic liver was found.
- 000
- 00000naa 2200000 a 4500
- 001
- bmc09004113
- 003
- CZ-PrNML
- 005
- 20231012103543.0
- 008
- 091127s2007 gw e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $d ABA008
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Mrkvicová, Alena. $7 xx0267751
- 245 10
- $a Expression of mRNAs related to connective tissue metabolism in rat hepatic stellate cells and myofibroblasts / $c Jiroutova A, Slavkovsky R, Cermakova M, Majdiakova L, Hanovcova I, Bolehovska R, Hajzlerova M, Radilova H, Ruszova E, Kanta J.
- 314 __
- $a Charles University in Prague, Faculty of Medicine in Hradec Kralove, Department of Medical Biochemistry, Simkova 870, 500 38 Hradec Kralove, Czech Republic
- 520 9_
- $a Hepatic stellate cells (HSC) and liver myofibroblasts (MFB) are two cell populations most likely responsible for the synthesis of most connective tissue components in fibrotic liver. They differ in their origin and location, and possibly in patterns of gene expression. Normal and carbon tetrachloride-cirrhotic livers from rats were used to isolate HSC. Liver was perfused with pronase and collagenase solutions, followed by centrifugation of the cell suspension on a density gradient. HSC were quiescent 2 days after plating on plastic but they became activated after another 5 days in culture. When the culture was passaged 5 times, its character changed profoundly as HSC were replaced by MFB. Microarray analysis was used to determine gene expression in quiescent HSC, activated HSC and MFB. The expression of 49 genes coding for connective tissue proteins, proteoglycans, metalloproteinases and their inhibitors, growth factors and cellular markers was determined. The pattern of gene expression changed during HSC activation and there were distinct differences between HSC and MFB. Little difference between normal cells and cells isolated from cirrhotic liver was found.
- 650 _2
- $a financování organizované $7 D005381
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a otrava chloridem uhličitým $7 D002252
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a pojivová tkáň $x metabolismus $x účinky léků $7 D003238
- 650 _2
- $a extracelulární matrix $x chemie $7 D005109
- 650 _2
- $a fibroblasty $x cytologie $x metabolismus $x účinky léků $7 D005347
- 650 _2
- $a exprese genu $7 D015870
- 650 _2
- $a imunohistochemie $7 D007150
- 650 _2
- $a játra $x cytologie $x metabolismus $x účinky léků $7 D008099
- 650 _2
- $a experimentální cirhóza jater $x metabolismus $7 D008106
- 650 _2
- $a metaloproteasy $x genetika $x metabolismus $7 D045726
- 650 _2
- $a myocyty hladké svaloviny $x cytologie $x metabolismus $x účinky léků $7 D032389
- 650 _2
- $a sekvenční analýza hybridizací s uspořádaným souborem oligonukleotidů $7 D020411
- 650 _2
- $a proteoglykany $x genetika $x metabolismus $7 D011509
- 650 _2
- $a messenger RNA $x biosyntéza $x účinky léků $7 D012333
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a polymerázová řetězová reakce s reverzní transkripcí $7 D020133
- 650 _2
- $a tkáňové inhibitory metaloproteinas $7 D019714
- 655 _2
- $a srovnávací studie $7 D003160
- 700 1_
- $a Slavkovský, Rastislav $7 xx0096675
- 700 1_
- $a Čermáková, Martina $7 xx0243170
- 700 1_
- $a Bittnerová, Lenka $7 xx0156439
- 700 1_
- $a Hanovcová, Irena $7 xx0064296
- 700 1_
- $a Bolehovská, Radka. $7 xx0195047
- 700 1_
- $a Hajzlerová, M. $7 _BN001844
- 700 1_
- $a Radilová, Hana $7 mzk2006348915
- 700 1_
- $a Ruszová, Ema $7 xx0109138
- 700 1_
- $a Kanta, Jiří, $d 1943- $7 xx0076201
- 773 0_
- $w MED00009709 $t Experimental and toxicologic pathology $g Roč. 58, č. 4 (2007), s. 263-273 $x 0940-2993
- 910 __
- $a ABA008 $b x $y 8 $z 0
- 990 __
- $a 20091123115031 $b ABA008
- 991 __
- $a 20231012103537 $b ABA008
- 999 __
- $a ok $b bmc $g 699931 $s 562343
- BAS __
- $a 3
- BMC __
- $a 2007 $b 58 $c 4 $d 263-273 $i 0940-2993 $m Experimental and toxicologic pathology $x MED00009709
- LZP __
- $a 2009-B3/dkme