利用三维芯片模型评估新型 ALK5 抑制剂 EW-7197 对肾脏纤维化的疗效。

IF 2.9 3区 医学 Q1 UROLOGY & NEPHROLOGY
So Young Jang, Seong-Hye Hwang, Yunyeong Choi, Wan-Young Kim, Sung Hyuk Park, Won Mook Kim, Eun-Jeong Kwon, Sejoong Kim
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引用次数: 0

摘要

背景:EW-7197是一种强效口服ALK5抑制剂,在三维(3D)肾脏纤维化芯片和小鼠模型中评估了它对转化生长因子β1(TGF-β1)诱导的纤维化的影响。评估内容包括肾小管上皮-间质转化、血管生成和炎性细胞因子表达:在三维肾纤维化芯片模型中,培养了三种细胞类型(肾成纤维细胞、人近端肾小管细胞系和人脐静脉内皮细胞),并用 TGF-β1 和 EW-7197 进行处理。评估了α-平滑肌肌动蛋白(α-SMA)和角蛋白 8(KRT-8)的表达,通过共聚焦显微镜观察了血管生成,并使用实时聚合酶链式反应、免疫测定和酶联免疫吸附试验测定了细胞因子水平。在顺铂诱导的肾纤维化小鼠模型中,测定了血尿素氮水平、TGF-β和Smad 2/3,并用马森三色染色法评估了肾纤维化:结果:EW-7197组的α-SMA表达明显低于TGF-β纤维化组。TGF-β 降低了上皮标志物 KRT-8 的表达,EW-7197 和 SB431542 逆转了这一效应。在 TGF-β 诱导的纤维化模型中,粗血管的长度缩短,粗细血管的直径均缩小,但 EW-7197 逆转了这些效应。EW-7197 明显降低了 TGF-β 的信使 RNA 表达,提高了血管内皮生长因子受体 2、白细胞介素 (IL)-10 和 IL-6 的水平。EW-7197 降低了分泌细胞因子 TGF-β1、TGF-β3 和 IL-1β 的水平。在顺铂诱导的肾纤维化小鼠模型中,EW-7197通过下调TGF-β信号传导减轻了肾纤维化:结论:在三维芯片模型和动物模型中,EW-7197可减轻TGF-β1诱导的纤维化细胞反应。这些研究结果表明了 EW-7197 在减轻肾脏纤维化方面的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the novel ALK5 inhibitor EW-7197 on therapeutic efficacy in renal fibrosis using a three-dimensional chip model.

Background: EW-7197, a potent oral ALK5 inhibitor, was assessed for its impact on transforming growth factor beta 1 (TGF-β1)-induced fibrosis in a three-dimensional (3D) renal fibrosis-on-a-chip and a mouse model. The evaluation included tubular epithelial-mesenchymal transition, angiogenesis, and inflammatory cytokine expression.

Methods: In a 3D renal fibrosis-on-a-chip model, three cell types (kidney fibroblasts, human proximal tubular cell line, and human umbilical vein endothelial cells) were cultured and treated with TGF-β1 and EW-7197. Expression of alpha smooth muscle actin (α-SMA) and keratin 8 (KRT-8) was assessed, angiogenesis was observed via confocal microscopy, and cytokine levels were measured using real-time polymerase chain reaction, immunoassay, and enzyme-linked immunosorbent assay. In a cisplatin-induced renal fibrosis mouse model, blood urea nitrogen levels, TGF-β, and Smad 2/3 were determined, and renal fibrosis was assessed with Masson's trichrome stain.

Results: The α-SMA expression was significantly lower in the EW-7197 group than in the TGF-β fibrosis group. TGF-β decreased the expression of the epithelial marker KRT-8, an effect that was reversed by EW-7197 and SB431542. In the TGF-β-induced fibrosis model, the length of the thick vessels was reduced, and the diameter of both thick and thin vessels was decreased, but EW-7197 reversed these effects. EW-7197 significantly reduced the messenger RNA expression of TGF-β and increased the levels of vascular endothelial growth factor receptor 2, interleukin (IL)-10, and IL-6. EW-7197 reduced the levels of secretory cytokines TGF-β1, TGF-β3, IL-1β. In the cisplatin-induced renal fibrosis mouse model, EW-7197 reduced renal fibrosis by down-regulating TGF-β signaling.

Conclusion: EW-7197 attenuated the TGF-β1-induced fibrotic cellular response in the 3D chip model and animal model. These findings indicate the potential effect of EW-7197 in attenuating renal fibrosis.

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来源期刊
CiteScore
4.60
自引率
10.00%
发文量
77
审稿时长
10 weeks
期刊介绍: Kidney Research and Clinical Practice (formerly The Korean Journal of Nephrology; ISSN 1975-9460, launched in 1982), the official journal of the Korean Society of Nephrology, is an international, peer-reviewed journal published in English. Its ISO abbreviation is Kidney Res Clin Pract. To provide an efficient venue for dissemination of knowledge and discussion of topics related to basic renal science and clinical practice, the journal offers open access (free submission and free access) and considers articles on all aspects of clinical nephrology and hypertension as well as related molecular genetics, anatomy, pathology, physiology, pharmacology, and immunology. In particular, the journal focuses on translational renal research that helps bridging laboratory discovery with the diagnosis and treatment of human kidney disease. Topics covered include basic science with possible clinical applicability and papers on the pathophysiological basis of disease processes of the kidney. Original researches from areas of intervention nephrology or dialysis access are also welcomed. Major article types considered for publication include original research and reviews on current topics of interest. Accepted manuscripts are granted free online open-access immediately after publication, which permits its users to read, download, copy, distribute, print, search, or link to the full texts of its articles to facilitate access to a broad readership. Circulation number of print copies is 1,600.
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