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改善皮肤表皮和真皮再生的脂质体基因转导的临床前评估。

Pre-clinical evaluation of liposomal gene transfer to improve dermal and epidermal regeneration.

机构信息

Shriners Hospitals for Children and University of Texas Medical Branch, Galveston, TX 77550, USA.

出版信息

Gene Ther. 2010 Jun;17(6):770-8. doi: 10.1038/gt.2010.32. Epub 2010 Apr 8.

Abstract

Liposomal gene transfer effectively enhances dermal and epidermal regeneration in burned rodents. To advance this treatment to clinical studies, we investigated the efficacy of liposomal gene transfer in a clinically relevant porcine wound model. Mimicking the clinical scenario, six female Yorkshire pigs (40-50 kg) received up to 12 burns of 50 cm(2) area that were fully excised and covered with skin autograft meshed at 4:1 ratio 24 h post-burn. Animals received control injections (empty liposomes), liposomes (DMRIE-C) containing 1 mg LacZ-cDNA, or liposomes (DMRIE-C) with 1 mg of platelet-derived growth factor (PDGF)-cDNA, or the naked PDGF gene. Serial biopsies were taken from different wound sites at multiple time points up to 12 days post-wounding. Transfection efficacy and transfection rate of LacZ and localization of beta-gal were determined by immunohistochemical and immunofluorescent techniques. RT-PCR and multiplex protein analysis (ELISA) were used to measure levels of growth factor mRNA transcribed and growth factor protein translated. Wound re-epithelialization and graft adhesion was evaluated using planimetric analysis and clinical scores. We found that peak transfection of liposomal beta-galactosidase occurred on day 2, with a fluorescence increase of 154% to baseline (P<0.001). Transfection intensity dropped to 115% above baseline on day 4 (P<0.001) and 109% on day 7. Immunohistochemistry showed a maximum transfection rate of 34% of cells in wound tissue. Gene transfer of liposomal PDGF-cDNA resulted in increased PDGF-mRNA and protein expression on days 2 and 4, and accelerated wound re-epithlialization as well as graft adhesion on day 9 (P<0.05). In this study, we showed that liposomal cDNA gene transfer is possible in a porcine wound model, and by using PDGF-cDNA we further showed that dermal and epidermal regeneration can be improved. These data indicate that liposomal gene transfer can be a new therapeutic approach to improve wound healing in humans.

摘要

脂质体基因转移有效地增强了烧伤啮齿动物的皮肤和表皮再生。为了将这种治疗方法推进到临床研究中,我们在一个临床相关的猪创伤模型中研究了脂质体基因转移的疗效。模拟临床情况,六头雌性约克夏猪(40-50 公斤)接受了多达 12 次 50cm² 面积的烧伤,烧伤后 24 小时,将这些烧伤完全切除并用 4:1 比例的皮肤自体移植物覆盖。动物接受对照注射(空脂质体)、含有 1mg LacZ-cDNA 的脂质体(DMRIE-C)或含有 1mg 血小板衍生生长因子(PDGF)-cDNA 的脂质体(DMRIE-C),或裸 PDGF 基因。在创伤后 12 天内的多个时间点,从不同的创伤部位连续采集活检。通过免疫组织化学和免疫荧光技术测定 LacZ 的转染效率和转染率以及β-半乳糖的定位。使用 RT-PCR 和多重蛋白分析(ELISA)测量转录的生长因子 mRNA 和翻译的生长因子蛋白的水平。使用平面分析和临床评分评估伤口再上皮化和移植物粘附。我们发现脂质体β-半乳糖苷酶的峰值转染发生在第 2 天,荧光增加了 154%(P<0.001)。第 4 天转染强度下降至基线以上 115%(P<0.001),第 7 天下降至 109%。免疫组织化学显示,伤口组织中最大转染率为 34%的细胞。脂质体 PDGF-cDNA 的基因转移导致第 2 天和第 4 天 PDGF-mRNA 和蛋白表达增加,并加速第 9 天的伤口再上皮化和移植物粘附(P<0.05)。在这项研究中,我们表明脂质体 cDNA 基因转移在猪创伤模型中是可行的,并且通过使用 PDGF-cDNA,我们进一步表明皮肤和表皮再生可以得到改善。这些数据表明,脂质体基因转移可能成为改善人类伤口愈合的一种新的治疗方法。

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