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Exp Toxicol Pathol ; 58(4): 263-73, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17056239

RESUMEN

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.


Asunto(s)
Tejido Conectivo/metabolismo , Fibroblastos/metabolismo , Hígado/metabolismo , Miocitos del Músculo Liso/metabolismo , ARN Mensajero/biosíntesis , Animales , Tetracloruro de Carbono/toxicidad , Células Cultivadas , Tejido Conectivo/efectos de los fármacos , Matriz Extracelular/química , Fibroblastos/citología , Fibroblastos/efectos de los fármacos , Expresión Génica , Inmunohistoquímica , Hígado/citología , Hígado/efectos de los fármacos , Cirrosis Hepática Experimental/metabolismo , Metaloproteasas/genética , Metaloproteasas/metabolismo , Miocitos del Músculo Liso/citología , Miocitos del Músculo Liso/efectos de los fármacos , Análisis de Secuencia por Matrices de Oligonucleótidos , Proteoglicanos/genética , Proteoglicanos/metabolismo , ARN Mensajero/efectos de los fármacos , Ratas , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Inhibidores Tisulares de Metaloproteinasas/genética , Inhibidores Tisulares de Metaloproteinasas/metabolismo
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