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Construction and identification of the recombinant hFcεRIα/RBL-2H3 cells.
Liu, Zhongcheng; Hao, Lifang; Wang, Nanan; Zhang, Su; Zhang, Nan; Xu, Zhenzhen; Yang, Yanlei; Zhang, Yanfen.
Afiliación
  • Liu Z; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China. Electronic address: liuzc@hbu.edu.cn.
  • Hao L; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China.
  • Wang N; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China.
  • Zhang S; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China.
  • Zhang N; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China.
  • Xu Z; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China.
  • Yang Y; College of Pharmaceutical Sciences, Hebei University, Baoding 071002, China; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China.
  • Zhang Y; Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Baoding 071002, China; Offices of Science and Technology, Hebei University, Baoding 071002, China. Electronic address: zhangjing@hbu.edu.cn.
Plasmid ; 98: 31-36, 2018 06.
Article en En | MEDLINE | ID: mdl-30213734
IgE/FcεRI signal pathway plays a crucial role in triggering allergic reactions, and there is no cross-recognition between IgE and FcεRI in human and rats. In order to obtain the hFcεRIα/ RBL-2H3 cell line, total RNA was extracted from U937 cells, and the human FcεRIα gene was obtained by RT-PCR technology. Then the amplified product was digested and inserted into the pIRES2-EGFP vector. After the plasmid was transfected into the RBL-2H3 cells using lipofectamine, and the RBL-2H3 cell lines of stable expression were screened by G418. The transfection efficiency reached 60.45% with optimizing transfection parameters. The last the expression of hFcεRIα was detected by RT-PCR, western blotting and fluorescent microscopy. The present results demonstrated that the pIRES2-EGFP-hFcεRIα vector was constructed and a stable cell line of hFcεRIα/ RBL-2H3 cells was established successfully. This cell line is promising tools for further research on the pathogenesis and drug development of allergic diseases.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Plásmidos / Inmunoglobulina E / Transfección / Leucemia Basofílica Aguda / Receptores de IgE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Plasmid Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Plásmidos / Inmunoglobulina E / Transfección / Leucemia Basofílica Aguda / Receptores de IgE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Plasmid Año: 2018 Tipo del documento: Article