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Tat-APE1/ref-1 protein inhibits TNF-alpha-induced endothelial cell activation.
Song, Yun Jeong; Lee, Ji Young; Joo, Hee Kyoung; Kim, Hyo Shin; Lee, Sang Ki; Lee, Kwon Ho; Cho, Chung-Hyun; Park, Jin Bong; Jeon, Byeong Hwa.
Afiliação
  • Song YJ; Research Institute of Medical Sciences, Department of Physiology, College of Medicine, Chungnam National University, 6 Munhwa-dong, Jung-gu, Daejeon 301-131, Republic of Korea.
Biochem Biophys Res Commun ; 368(1): 68-73, 2008 Mar 28.
Article em En | MEDLINE | ID: mdl-18206643
ABSTRACT
Apurinic/apyrimidinic endonuclease 1/redox factor-1 (APE1/ref-1) is a multifunctional protein involved both in DNA base excision repair and redox regulation. In this study we evaluated the protective role of Tat-mediated APE1/ref-1 transduction on the tumor necrosis factor (TNF)-alpha-activated endothelial activation in cultured human umbilical vein endothelial cells. To construct Tat-APE1/ref-1 fusion protein, human full length of APE1/ref-1 was fused with Tat-protein transduction domain. Purified Tat-APE1/ref-1 fusion protein efficiently transduced cultured endothelial cells in a dose-dependent manner and reached maximum expression at 1h after incubation. Transduced Tat-APE1/ref-1 showed inhibitory activity on the TNF-alpha-induced monocyte adhesion and vascular cell adhesion molecule-1 expression in cultured endothelial cells. These results suggest Tat-APE1/ref-1 might be useful to reduce vascular endothelial activation or vascular inflammatory disorders.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Produtos do Gene tat / Fator de Necrose Tumoral alfa / Células Endoteliais / DNA Liase (Sítios Apurínicos ou Apirimidínicos) Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Produtos do Gene tat / Fator de Necrose Tumoral alfa / Células Endoteliais / DNA Liase (Sítios Apurínicos ou Apirimidínicos) Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2008 Tipo de documento: Article