RGD肽水凝胶下调机械信号YAP抑制术后瘢痕形成。

Yao Lv, Licheng Liang, Mian Qin, Ru-Ping Jiang, Fei-Fei Zong, Xia Wu, Kai-Li Wu, Liang Liang
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引用次数: 0

摘要

目的:青光眼滤过失败可能是由过多的人Tenon囊成纤维细胞(HTFs)形成滤过道疤痕引起的。相反,yes相关蛋白(YAP)是Hippo信号通路的转录激活因子,是基质产生和成纤维细胞激活的关键基质刚度调节剂。RGD肽水凝胶具有良好的生物相容性和可生物降解性,模拟了真实组织的细胞外基质(ECM)结构。本研究的目的是确定通过RGD肽水凝胶下调YAP表达是否可以阻止HTFs的激活和ECM蛋白的分泌。利用转化生长因子-β2 (TGF-β2)诱导青光眼滤过术后瘢痕形成细胞模型中HTFs的活化。采用SD大鼠建立小鼠结膜下损伤模型。Masson染色观察胶原纤维形态,免疫组化检测YAP和α-平滑肌肌动蛋白(α-SMA)的表达。在小鼠眼损伤模型中发现RGD肽水凝胶具有抗瘢痕形成的特性,并且能够减少HTFs的激活、YAP的表达、胞质核的积累以及结缔组织生长因子(CTGF)和ECM蛋白的表达。结果表明,其最佳浓度为1.0%。该浓度不仅可以在体内更容易地在结膜下注射药物,维持结膜滤过囊空间,还可以抑制成纤维细胞向肌成纤维细胞的活化,下调Tenon胶囊成纤维细胞中hipo - yap信号通路的表达。意义陈述:1;1.0%凝胶的内部结构为均匀的网状三维纳米结构,具有良好的给药特性,可实现长效控释。2. RGD肽水凝胶具有一定的基质硬度,能模拟正常结膜下结缔组织硬度。3. RGD肽水凝胶可抑制大鼠结膜纤维化的发生。4. RGD肽水凝胶可抑制HTFs中YAP及其靶基因CTGF以及α-SMA、ECM蛋白的表达。5. RGD肽水凝胶具有良好的生物相容性、生物可降解性和稳定的力学性能,是一种很有前景的药物控释载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RGD peptide hydrogel downregulates mechanosignal YAP to inhibit postoperative scarring.

Objective: Glaucoma filtration failure may result from an overabundance of human Tenon's capsule fibroblasts (HTFs) forming a filtration tract scar. Conversely, the Yes-associated protein (YAP), a transcriptional activator of the Hippo signaling pathway, is a crucial matrix stiffness regulator of matrix production and fibroblast activation. With superior biocompatibility and biodegradability, RGD peptide hydrogels imitate the structure of real tissues' extracellular matrix (ECM). The purpose of this research was to determine whether down-regulating YAP expression via RGD peptide hydrogels may prevent HTFs activation and ECM protein secretion. Transforming growth factor-β2 (TGF-β2) was used to induce the activation of HTFs in a cellular model of scarring following glaucoma filtration surgery. Utilizing SD rats, a murine model of subconjunctival injury was established. The shape of collagen fibers was observed through Masson staining, and the expression of YAP and α-smooth muscle actin (α-SMA) was identified through immunohistochemistry. RGD peptide hydrogel was discovered to have anti-scarring properties in a mouse eye injury model, as well as the ability to lessen HTFs activation, YAP expression, cytosolic nucleus accumulation, and the expression of connective tissue growth factor (CTGF) and ECM proteins. The best concentration was found to be 1.0 weight percent among them. This concentration not only makes it easier to inject a drug subconjunctivally in vivo and maintain the filtration vesicle space in the conjunctiva, but it also inhibits the activation of fibroblasts into myofibroblasts and down-regulates the expression of the Hippo-YAP signaling pathway in Tenon's capsule fibroblasts.

Statement of significance: 1. The homogenous reticular three-dimensional nanostructure that made up the interior structure of the 1.0 weight percent gel had good drug delivery characteristics for long-lasting controlled drug release. 2. RGD peptide hydrogel had a certain matrix hardness, which could mimic the normal connective tissue hardness under the conjunctiva. 3. RGD peptide hydrogels could prevented the development of rat conjunctival fibrosis. 4. RGD peptide hydrogel could inhibit the expression of YAP and its target gene CTGF, as well as α-SMA, ECM proteins in HTFs. 5. RGD peptide hydrogel has good biocompatibility, biodegradability, and stable mechanical properties, and can also be used as a promising carrier for the controlled release of drugs.

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