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Kv4.3 Modulates the Distribution of hERG.
Zhao, Xiao-Jing; Zhu, Chao; Tian, Liu-Yang; Fu, Yi-Cheng; Zhang, Yu; Chen, Xi; Huang, Yun; Li, Yang.
Afiliación
  • Zhao XJ; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China.
  • Zhu C; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China.
  • Tian LY; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China.
  • Fu YC; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China.
  • Zhang Y; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China.
  • Chen X; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China.
  • Huang Y; Department of Gerontology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. huangyun1207@163.com.
  • Li Y; Department of Cardiology, General Hospital of Chinese People's Liberation Army, Beijing, China. liyangxys@163.com.
Sci Rep ; 7(1): 17757, 2017 12 19.
Article en En | MEDLINE | ID: mdl-29259226
This study examines the interaction between hERG and Kv4.3. The functional interaction between hERG and Kv4.3, expressed in a heterologous cell line, was studied using patch clamp techniques, western blot, immunofluorescence, and co-immunoprecipitation. Co-expression of Kv4.3 with hERG increased hERG current density (tail current after a step to +10 mV: 26 ± 3 versus 56 ± 7 pA/pF, p < 0.01). Kv4.3 co-expression also increased the protein expression and promoted the membrane localization of hERG. Western blot showed Kv4.3 increased hERG expression by Hsp70. hERG and Kv4.3 co-localized and co-immunoprecipitated in cultured 293 T cells, indicating physical interactions between hERG and Kv4.3 proteins in vitro. In addition, Hsp70 interacted with hERG and Kv4.3 respectively, and formed complexes with hERG and Kv4.3. The α subunit of Ito Kv4.3 can interact with and modify the localization of the α subunit of IKr hERG, thus providing potentially novel insights into the molecular mechanism of the malignant ventricular arrhythmia in heart failure.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Membrana Celular / Proteínas HSP70 de Choque Térmico / Complejos Multiproteicos / Canales de Potasio Shal / Canal de Potasio ERG1 Límite: Humans Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Membrana Celular / Proteínas HSP70 de Choque Térmico / Complejos Multiproteicos / Canales de Potasio Shal / Canal de Potasio ERG1 Límite: Humans Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido