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经皮 TGFβ1-337 双链 RNA 贴剂治疗增生性瘢痕。

Transdermal siRNA-TGFβ1-337 patch for hypertrophic scar treatment.

机构信息

Institute of Molecular Biology, Southern Medical University, Guangzhou 510515, PR China.

出版信息

Matrix Biol. 2013 Jun 24;32(5):265-76. doi: 10.1016/j.matbio.2013.02.004. Epub 2013 Mar 5.

Abstract

Hypertrophic scarring (HSc) is a fibroproliferative disorder of the dermis characterized by erythematous, swollen, and pruritic lesions of healing skin. An increased understanding of the role of TGFβ1 in the development of HSc provides the potential for treating HSc by down-regulating TGFβ1 expression. siRNAs that effectively interfered with TGFβ1 expression were screened. It was concluded that the siRNA-TGFβ1-337 was able to effectively down-regulate TGFβ1 expression in HSc fibroblasts. The effects of siRNA-TGFβ1-337 on cell proliferation, cell cycle, and apoptosis of HSc fibroblasts were investigated. It was shown that it inhibited cell proliferation, arrested cells in the G1 stage of the cell cycle, and induced apoptosis of HSc fibroblasts. The transdermal patch of siRNA-TGFβ1-337 was a combination of siRNA-TGFβ1-337 and a pressure-sensitive adhesive hydrogel. The treatment effects of the transdermal patch were assessed in an animal model established by transplanting human HSc to nude mice. Decreased expression of TGFβ1 was observed with treatment with the transdermal siRNA-TGFβ1-337 patch. Consequently, the treatment resulted in type I collagen down-regulation and regularly arranged scar fibroblasts being significantly reduced and undergoing apoptosis; the scar size was decreased significantly. Thus, our findings indicate that a transdermal siRNA-TGFβ1-337 patch is a potential treatment for hypertrophic scars.

摘要

增生性瘢痕(HSc)是一种真皮纤维增生性疾病,其特征为愈合皮肤的红斑、肿胀和瘙痒性病变。对 TGFβ1 在 HSc 发展中的作用的深入了解为通过下调 TGFβ1 表达来治疗 HSc 提供了潜力。筛选出能有效干扰 TGFβ1 表达的 siRNAs。结论是,siRNA-TGFβ1-337 能够有效下调 HSc 成纤维细胞中的 TGFβ1 表达。研究了 siRNA-TGFβ1-337 对 HSc 成纤维细胞增殖、细胞周期和凋亡的影响。结果表明,它抑制细胞增殖,使细胞周期停滞在 G1 期,并诱导 HSc 成纤维细胞凋亡。siRNA-TGFβ1-337 的透皮贴剂是 siRNA-TGFβ1-337 和压敏性水凝胶的组合。通过将人 HSc 移植到裸鼠中建立动物模型,评估了透皮 siRNA-TGFβ1-337 贴剂的治疗效果。用透皮 siRNA-TGFβ1-337 贴剂治疗后观察到 TGFβ1 表达下调。因此,该治疗导致 I 型胶原下调,排列整齐的瘢痕成纤维细胞明显减少并发生凋亡;瘢痕大小明显减小。因此,我们的研究结果表明,透皮 siRNA-TGFβ1-337 贴剂是治疗增生性瘢痕的一种潜在治疗方法。

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