中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
11期
1743-1748
,共6页
张有斌%余云生%沈振亚%周东明
張有斌%餘雲生%瀋振亞%週東明
장유빈%여운생%침진아%주동명
组织构建%组织工程%器官移植%重组腺病毒Adc68%TIPE2基因%基因表达%转染%T细胞
組織構建%組織工程%器官移植%重組腺病毒Adc68%TIPE2基因%基因錶達%轉染%T細胞
조직구건%조직공정%기관이식%중조선병독Adc68%TIPE2기인%기인표체%전염%T세포
adenoviridae%gene expression%transfection
背景:TIPE2抗炎蛋白,通过对T细胞受体(TCR)和T细胞TOLL样受体信号途径实行负向调节,从而对适应性免疫和固有免疫起到负性调控作用,有效地维持机体内环境的稳定。<br> 目的:使用人工合成腺病毒载体构建能过表达大鼠TIPE2基因的重组腺病毒。<br> 方法:利用RT-PCR的方法,从大鼠淋巴细胞中扩增出大鼠TIPE2基因,克隆到穿梭质粒pShuttle-clontech的表达框中,然后将包含TIPE2的完整表达框,进一步亚克隆到黑猩猩来源的腺病毒包装载体AdC68,转染HEK 293A细胞,包装出重组腺病毒。并以其感染HEK293A细胞,采用western blotting方法检测TIPE2基因的表达水平。<br> 结果与结论:PCR扩增、酶切鉴定和测序结果表明,所获取的cDNA为TIPE2的蛋白编码基因,western blotting结果表明,重组腺病毒能可高效表达TIPE2基因。说明成功完成AdC68-TIPE2重组腺病毒的构建,该腺病毒载体,能稳定表达大鼠TIPE2基因。
揹景:TIPE2抗炎蛋白,通過對T細胞受體(TCR)和T細胞TOLL樣受體信號途徑實行負嚮調節,從而對適應性免疫和固有免疫起到負性調控作用,有效地維持機體內環境的穩定。<br> 目的:使用人工閤成腺病毒載體構建能過錶達大鼠TIPE2基因的重組腺病毒。<br> 方法:利用RT-PCR的方法,從大鼠淋巴細胞中擴增齣大鼠TIPE2基因,剋隆到穿梭質粒pShuttle-clontech的錶達框中,然後將包含TIPE2的完整錶達框,進一步亞剋隆到黑猩猩來源的腺病毒包裝載體AdC68,轉染HEK 293A細胞,包裝齣重組腺病毒。併以其感染HEK293A細胞,採用western blotting方法檢測TIPE2基因的錶達水平。<br> 結果與結論:PCR擴增、酶切鑒定和測序結果錶明,所穫取的cDNA為TIPE2的蛋白編碼基因,western blotting結果錶明,重組腺病毒能可高效錶達TIPE2基因。說明成功完成AdC68-TIPE2重組腺病毒的構建,該腺病毒載體,能穩定錶達大鼠TIPE2基因。
배경:TIPE2항염단백,통과대T세포수체(TCR)화T세포TOLL양수체신호도경실행부향조절,종이대괄응성면역화고유면역기도부성조공작용,유효지유지궤체내배경적은정。<br> 목적:사용인공합성선병독재체구건능과표체대서TIPE2기인적중조선병독。<br> 방법:이용RT-PCR적방법,종대서림파세포중확증출대서TIPE2기인,극륭도천사질립pShuttle-clontech적표체광중,연후장포함TIPE2적완정표체광,진일보아극륭도흑성성래원적선병독포장재체AdC68,전염HEK 293A세포,포장출중조선병독。병이기감염HEK293A세포,채용western blotting방법검측TIPE2기인적표체수평。<br> 결과여결론:PCR확증、매절감정화측서결과표명,소획취적cDNA위TIPE2적단백편마기인,western blotting결과표명,중조선병독능가고효표체TIPE2기인。설명성공완성AdC68-TIPE2중조선병독적구건,해선병독재체,능은정표체대서TIPE2기인。
BACKGROUND:Tumor necrosis factor-α-induced protein-8 like-2 (TIPE2), an anti-inflammatory protein, through the T cel receptor (TCR) and TOLL-like receptor signaling pathway, implements negative regulation of adaptive immunity and innate immunity, and thus effectively maintains the stable internal environment of the body. <br> OBJECTIVE:To construct a recombinant adenovirus that can overexpress rat TIPE2 gene. <br> METHODS:TIPE2 cDNA target gene was amplified from rat’s lymphocytes using RT-PCR, cloned into shuttle plasmid pShuttle-clontech, and then subcloned into artificial adenovirus vector AdC68. Hereafter, HEK 293 cel s were transfected to generate a recombinant adenovirus. HEK293A cel s were infected using this recombinant adenovirus, and then TIPE2 gene level was tested by western blot method. <br> RESULTS AND CONCLUSION:Based on results of PCR, digestion identification and sequencing, the obtained cDNA was the coding sequence region of TIPE2. Western blot findings showed that the recombinant adenovirus could overexpress TIPE2 gene. These findings indicate that the recombinant adenovirus is constructed successful y and can express TIPE2 gene stably.