2002Zhonghua ganzangbing zazhiRequires access

Effect of lovastatin on proliferation and extracellular matrix secretion of rat hepatic stellate cells in vitro

LI Sh

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Abstract

Objective To investigate the effect of lovastatin on proliferation and extracellular matrix secretion of hepatic stellate cells in vitro. Methods Rat hepatic stellate cells were incubated with different concentration of lovastatin and geranyl geranypyrophosphate. Cell proliferation was assessed by MTT colorimetric assay. Cell cycle was analysed by flow cytometry. Type IV collagen and laminin were determined by ELISA, and c-jun and c-fos expression by immunocy-tochemistry and computer video text analysis system. Results Addition of 0.1-50 μmol/L lovastatin into culture medium had no toxicity to hepatic stellate cells, but could significantly inhibite hepatic stellate cell proliferation and provoke G0/G1 phase arrest in dose-dependent manner, and could also markedly inhibit the c-jun and c-fos expression and type IV collagen and laminin secretion, which could partly be antagonized by geranyl geranypyrophosphate. Conclusions Lovastatin can significantly inhibite hepatic stellate cell proliferation and type IV collagen and laminin secretion, which might be partly related to its inhibitory effect on geranyl geranypyrophosphate formation.

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Objective To investigate the effect of lovastatin on proliferation and extracellular matrix secretion of hepatic stellate cells in vitro. Methods Rat hepatic stellate cells were incubated with different concentration of lovastatin and geranyl geranypyrophosphate. Cell proliferation was assessed by MTT colorimetric assay. Cell cycle was analysed by flow cytometry. Type IV collagen and laminin were determined by ELISA, and c-jun and c-fos expression by immunocy-tochemistry and computer video text analysis system. Results Addition of 0.1-50 μmol/L lovastatin into culture medium had no toxicity to hepatic stellate cells, but could significantly inhibite hepatic stellate cell proliferation and provoke G0/G1 phase arrest in dose-dependent manner, and could also markedly inhibit the c-jun and c-fos expression and type IV collagen and laminin secretion, which could partly be antagonized by geranyl geranypyrophosphate. Conclusions Lovastatin can significantly inhibite hepatic stellate cell proliferation and type IV collagen and laminin secretion, which might be partly related to its inhibitory effect on geranyl geranypyrophosphate formation.

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Available abstract

Objective To investigate the effect of lovastatin on proliferation and extracellular matrix secretion of hepatic stellate cells in vitro. Methods Rat hepatic stellate cells were incubated with different concentration of lovastatin and geranyl geranypyrophosphate. Cell proliferation was assessed by MTT colorimetric assay. Cell cycle was analysed by flow cytometry. Type IV collagen and laminin were determined by ELISA, and c-jun and c-fos expression by immunocy-tochemistry and computer video text analysis system. Results Addition of 0.1-50 μmol/L lovastatin into culture medium had no toxicity to hepatic stellate cells, but could significantly inhibite hepatic stellate cell proliferation and provoke G0/G1 phase arrest in dose-dependent manner, and could also markedly inhibit the c-jun and c-fos expression and type IV collagen and laminin secretion, which could partly be antagonized by geranyl geranypyrophosphate. Conclusions Lovastatin can significantly inhibite hepatic stellate cell proliferation and type IV collagen and laminin secretion, which might be partly related to its inhibitory effect on geranyl geranypyrophosphate formation.

Key concepts: Hepatic stellate cell, Lovastatin, Laminin, Extracellular matrix, Secretion, Cell growth, In vitro, Chemistry

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