Suppr超能文献

模仿异常肾系膜基质的纳米图案支架对系膜细胞行为的影响。

The Influence of a Nanopatterned Scaffold that Mimics Abnormal Renal Mesangial Matrix on Mesangial Cell Behavior.

机构信息

Department of Nanoscience and Nanoengineering, Graduate School of Advanced Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, Japan.

Cellular Functional Nanobiomaterials Group, Research Center for Functional Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.

出版信息

Int J Mol Sci. 2019 Oct 28;20(21):5349. doi: 10.3390/ijms20215349.

Abstract

The alteration of mesangial matrix (MM) components in mesangium, such as type IV collagen (COL4) and type I collagen (COL1), is commonly found in progressive glomerular disease. Mesangial cells (MCs) responding to altered MM, show critical changes in cell function. This suggests that the diseased MM structure could play an important role in MC behavior. To investigate how MC behavior is influenced by the diseased MM 3D nanostructure, we fabricated the titanium dioxide (TiO)-based nanopatterns that mimic diseased MM nanostructures. Immortalized mouse MCs were used to assess the influence of disease-mimic nanopatterns on cell functions, and were compared with a normal-mimic nanopattern. The results showed that the disease-mimic nanopattern induced disease-like behavior, including increased proliferation, excessive production of abnormal MM components (COL1 and fibronectin) and decreased normal MM components (COL4 and laminin α1). In contrast, the normal-mimic nanopattern actually resulted in cells displaying normal proliferation and the production of normal MM components. In addition, increased expressions of α-smooth muscle actin (α-SMA), transforming growth factor β1 (TGF-β1) and integrin α5β1 were detected in cells grown on the disease-mimic nanopattern. These results indicated that the disease-mimic nanopattern induced disease-like cell behavior. These findings will help further establish a disease model that mimics abnormal MM nanostructures and also to elucidate the molecular mechanisms underlying glomerular disease.

摘要

系膜基质(MM)成分的改变,如 IV 型胶原(COL4)和 I 型胶原(COL1),在进行性肾小球疾病中很常见。对改变的 MM 有反应的系膜细胞(MC)在细胞功能上表现出关键的变化。这表明病变的 MM 结构可能在 MC 行为中起重要作用。为了研究 MC 行为如何受到病变 MM 3D 纳米结构的影响,我们制备了模仿病变 MM 纳米结构的二氧化钛(TiO)基纳米图案。永生小鼠 MC 用于评估疾病模拟纳米图案对细胞功能的影响,并与正常模拟纳米图案进行比较。结果表明,疾病模拟纳米图案诱导类似疾病的行为,包括增殖增加、异常 MM 成分(COL1 和纤维连接蛋白)过度产生和正常 MM 成分(COL4 和层粘连蛋白α1)减少。相比之下,正常模拟纳米图案实际上导致细胞表现出正常的增殖和正常 MM 成分的产生。此外,在疾病模拟纳米图案上生长的细胞中检测到α-平滑肌肌动蛋白(α-SMA)、转化生长因子β1(TGF-β1)和整合素α5β1的表达增加。这些结果表明疾病模拟纳米图案诱导了类似疾病的细胞行为。这些发现将有助于进一步建立模拟异常 MM 纳米结构的疾病模型,并阐明肾小球疾病的分子机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验