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Time course of TGFβ_1 and VEGF expression in experimental vein grafts

HU Hai-di

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Abstract

Objective To investigate time course of TGFβ 1 and VEGF expression and their role in intimal hyperplasia. [WT5”HZ]Methods[WT5”BZ] In situ hybridization and immunohistochemical technique were used to detect the time course of intimal hyperplasia, time course of TGFβ 1 mRNA and protein expression of TGFβ 1 and VEGF. [WT5”HZ]Results[WT5”BZ]After autogenous vein replacement, the obvious neointima was seen at 2 weeks, and peaked at 8 weeks. The expression of TGFβ 1 mRNA peaked at 1 week and decreased gradually, but at 10 weeks, its positive cell percentage was still 10 1%. Both protein expression of TGFβ 1 and VEGF in VSMCs increased from 24 hours after grafting and peaked at 2 weeks. Their positive cell percentages were 40 6% and 36 6% respectively. After 4 weeks, their expression decreased at 8 weeks, the positive cell percentages were 8 9% and 13 8% respectively. [WT5”HZ]Conclusions[WT5”BZ] TGFβ 1 plays an important part in ECM accumulation by promoting ECM synthelization and decreasing ECM degradation. VEGF plays the key role in reendothelialization. They may affect each other and cooperated in the formation of intimal hyperplasia.

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Objective To investigate time course of TGFβ 1 and VEGF expression and their role in intimal hyperplasia. [WT5”HZ]Methods[WT5”BZ] In situ hybridization and immunohistochemical technique were used to detect the time course of intimal hyperplasia, time course of TGFβ 1 mRNA and protein expression of TGFβ 1 and VEGF. [WT5”HZ]Results[WT5”BZ]After autogenous vein replacement, the obvious neointima was seen at 2 weeks, and peaked at 8 weeks. The expression of TGFβ 1 mRNA peaked at 1 week and decreased gradually, but at 10 weeks, its positive cell percentage was still 10 1%. Both protein expression of TGFβ 1 and VEGF in VSMCs increased from 24 hours after grafting and peaked at 2 weeks. Their positive cell percentages were 40 6% and 36 6% respectively. After 4 weeks, their expression decreased at 8 weeks, the positive cell percentages were 8 9% and 13 8% respectively. [WT5”HZ]Conclusions[WT5”BZ] TGFβ 1 plays an important part in ECM accumulation by promoting ECM synthelization and decreasing ECM degradation. VEGF plays the key role in reendothelialization. They may affect each other and cooperated in the formation of intimal hyperplasia.

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Available abstract

Objective To investigate time course of TGFβ 1 and VEGF expression and their role in intimal hyperplasia. [WT5”HZ]Methods[WT5”BZ] In situ hybridization and immunohistochemical technique were used to detect the time course of intimal hyperplasia, time course of TGFβ 1 mRNA and protein expression of TGFβ 1 and VEGF. [WT5”HZ]Results[WT5”BZ]After autogenous vein replacement, the obvious neointima was seen at 2 weeks, and peaked at 8 weeks. The expression of TGFβ 1 mRNA peaked at 1 week and decreased gradually, but at 10 weeks, its positive cell percentage was still 10 1%. Both protein expression of TGFβ 1 and VEGF in VSMCs increased from 24 hours after grafting and peaked at 2 weeks. Their positive cell percentages were 40 6% and 36 6% respectively. After 4 weeks, their expression decreased at 8 weeks, the positive cell percentages were 8 9% and 13 8% respectively. [WT5”HZ]Conclusions[WT5”BZ] TGFβ 1 plays an important part in ECM accumulation by promoting ECM synthelization and decreasing ECM degradation. VEGF plays the key role in reendothelialization. They may affect each other and cooperated in the formation of intimal hyperplasia.

Key concepts: Neointima, Intimal hyperplasia, In situ hybridization, Hyperplasia, Immunohistochemistry, Transforming growth factor, Cell, Andrology

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