目的 構(gòu)建含有由抗腫瘤相關(guān)糖蛋白72(anti-TAG72)單鏈抗體片段(single chain variable fragment,scFv)及CD28胞內(nèi)區(qū)及跨膜區(qū)的融合基因anti-TAG72 scFv-CD28的重組綠色熒光表達載體pEGFP-C3-anti-TAG72 scFv-CD28,并轉(zhuǎn)染獲得嵌合錨定T淋巴細胞。
方法 將anti-TAG72單鏈抗體及CD28胞內(nèi)區(qū)及跨膜區(qū)基因的嵌合錨定融合分子克隆入綠色熒光蛋白真核表達載體pEGFP-C3,獲得pEGFP-C3-anti-TAG72 scFv-CD28表達載體。用卡那霉素篩選陽性克隆,經(jīng)酶切和測序鑒定。將上述重組質(zhì)粒pEGFP-C3-anti-TAG72 scFv-CD28以脂質(zhì)體法瞬時轉(zhuǎn)染外周血單核細胞(PBMC),以獲得嵌合錨定T淋巴細胞,用熒光顯微鏡檢測嵌合分子anti-TAG72 scFv-CD28在PBMC中的表達,并檢驗嵌合錨定融合分子anti-TAG72 scFv-CD28的表達。
結(jié)果 重組綠色熒光表達載體pEGFP-C3-anti-TAG72 scFv-CD28中anti-TAG72 scFv-CD28片段為1 002 bp,與已知的序列相符。酶切、測序結(jié)果表明,嵌合錨定融合分子基因片段anti-TAG72 scFv-CD28被正確插入pEGFP-C3載體; 轉(zhuǎn)染后anti-TAG72 scFv-CD28片段及綠色熒光物質(zhì)表達于嵌合錨定T淋巴細胞胞膜表面及胞漿中,為綠色熒光顯色。
結(jié)論 完成了綠色熒光表達載體pEGFP-C3-anti-TAG72 scFv-CD28的構(gòu)建,并成功在PBMC瞬時表達。
引用本文: 徐宏勇,徐立,李開宗,竇科峰. 嵌合錨定融合分子在T淋巴細胞的熒光表達及檢測. 中國普外基礎(chǔ)與臨床雜志, 2010, 17(10): 1046-1049. doi: 復(fù)制
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2. | 徐立, 徐宏勇, 樊代明. 胃腸道腫瘤靶向抗癌胚抗原單鏈抗體與T淋巴細胞表面受體基因的融合分子構(gòu)建 [J]. 中華消化雜志, 2004; 24(2): 75-77. |
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9. | Hombach AA, Schildgen V, Heuser C, et al. T cell activation by antibody-like immunoreceptors: the position of the binding epitope within the target molecule determines the efficiency of activation of redirected T cells [J]. J Immunol, 2007; 178(7): 4650-4657. |
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11. | Compte M, Cuesta AM, Sánchez-Martín D, et al. Tumor immunotherapy using gene-modified human mesenchymal stem cells loaded into synthetic extracellular matrix scaffolds [J]. Stem Cells, 2009; 27(3): 753-760. |
12. | 徐宏勇, 徐立, 李開宗, 等. 癌胚抗原嵌合錨定T細胞對胃癌的體內(nèi)外抑癌效應(yīng)觀察 [J]. 中華外科雜志, 2008; 46(2): 148-149. |
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- 1. 徐宏勇, 徐立, 李開宗, 等. 靶向性腫瘤相關(guān)抗原TAG-72的scFv-CD28融合基因的真核表達載體的構(gòu)建 [J]. 中國普外基礎(chǔ)與臨床雜志, 2002; 9(6): 398-401.
- 2. 徐立, 徐宏勇, 樊代明. 胃腸道腫瘤靶向抗癌胚抗原單鏈抗體與T淋巴細胞表面受體基因的融合分子構(gòu)建 [J]. 中華消化雜志, 2004; 24(2): 75-77.
- 3. 徐宏勇, 徐立, 高建宏, 等. 嵌合錨定T細胞致癌胚抗原陽性胃癌細胞的凋亡效應(yīng) [J]. 中華醫(yī)學(xué)雜志, 2007; 87(15): 1053-1057.
- 4. Chmielewski M, Hombach A, Heuser C, et al. T cell activation by antibody-like immunoreceptors: increase in affinity of the single-chain fragment domain above threshold does not increase T cell activation against antigen-positive target cells but decreases selectivity [J]. J Immunol, 2004; 173(12): 7647-7653.
- 5. Alvarez-Vallina L, Hawkins RE. Antigen-specific targeting of CD28-mediated T cell co-stimulation using chimeric single-chain antibody variable fragment-CD28 receptors [J]. Eur J Immunol, 1996; 26(10): 2304-2309.
- 6. Hombach A, Heuser C, Marquardt T, et al. CD4+ T cells engrafted with a recombinant immunoreceptor efficiently lyse target cells in a MHC antigen- and Fas-independent fashion [J]. J Immunol, 2001; 167(2): 1090-1096.
- 7. Hombach A, Sent D, Schneider C, et al. T-cell activation by recombinant receptors: CD28 costimulation is required for interleukin 2 secretion and receptor-mediated T-cell proliferation but does not affect receptor-mediated target cell lysis [J]. Cancer Res, 2001; 61(5): 1976-1982.
- 8. Heuser C, Hombach A, Lsch C, et al. T-cell activation by recombinant immunoreceptors: impact of the intracellular signalling domain on the stability of receptor expression and antigen-specific activation of grafted T cells [J]. Gene Ther, 2003; 10(17): 1408-1419.
- 9. Hombach AA, Schildgen V, Heuser C, et al. T cell activation by antibody-like immunoreceptors: the position of the binding epitope within the target molecule determines the efficiency of activation of redirected T cells [J]. J Immunol, 2007; 178(7): 4650-4657.
- 10. Alonso-Camino V, Sánchez-Martín D, Compte M, et al. Lymphocyte display: a novel antibody selection platform based on T cell activation [J]. PLoS One, 2009; 4(9): e7174.
- 11. Compte M, Cuesta AM, Sánchez-Martín D, et al. Tumor immunotherapy using gene-modified human mesenchymal stem cells loaded into synthetic extracellular matrix scaffolds [J]. Stem Cells, 2009; 27(3): 753-760.
- 12. 徐宏勇, 徐立, 李開宗, 等. 癌胚抗原嵌合錨定T細胞對胃癌的體內(nèi)外抑癌效應(yīng)觀察 [J]. 中華外科雜志, 2008; 46(2): 148-149.
- 13. 馮百歲, 姚雪華, 趙國強. 幽門螺桿菌細胞毒素相關(guān)基因A綠色熒光蛋白真核表達載體的構(gòu)建 [J]. 中華醫(yī)學(xué)雜志, 2007; 87(8): 570-572.