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[Construction of rat interleukin-10 adenoviral vector and its expression in bone marrow mesenchymal stem cells].
Zhang, Wen-Ting; Tang, Juan; Zhao, Hong-Mei; You, Jie-Yu.
Afiliação
  • Zhang WT; Department of Gastroenterology, Hunan Children's Hospital, Changsha 410007, China. yjy660111@sina.com.
Zhongguo Dang Dai Er Ke Za Zhi ; 21(7): 708-712, 2019 Jul.
Article em Zh | MEDLINE | ID: mdl-31315773
OBJECTIVE: To construct the recombinant adenoviral vector carrying the rat interleukin-10 (rIL-10) gene, and to investigate whether it is stably expressed in bone marrow mesenchymal stem cells. METHODS: The rIL-10 gene was amplified by PCR from template rIL-10 cDNA, and the recovered 656 bp rIL-10 DNA fragment was cloned into pcDNA3.1 to construct pcDNA3.1-IL-10. Then HEK293 cells were transfected with pcDNA3.1-IL-10 and adenoviral vector for homologous recombination, and sequencing and PCR were used to evaluate whether recombination was successful. HEK293 cells were lysed by repeated freeze-thaw cycles, and bone marrow mesenchymal stem cells were infected with the virus solution containing the rIL-10 gene. Western blot was used to measure the expression of rIL-10 in bone marrow mesenchymal stem cells. RESULTS: Sequencing and PCR verified that the rIL-10 adenoviral vector was successfully constructed, with a virus titer of 4×109 PFU/mL. The expression of IL-10 was detected after bone marrow mesenchymal stem cells were infected by the virus solution containing the rIL-10 gene. CONCLUSIONS: The constructed rIL-10 recombinant adenovirus can mediate the stable expression of rIL-10 gene in bone marrow mesenchymal stem cells, which provides a basis for gene transplantation therapy of inflammatory bowel disease.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Mesenquimais Limite: Animals / Humans Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células-Tronco Mesenquimais Limite: Animals / Humans Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article