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使用逐层沉积法进行同步心脏宏观组织的多维组装。

Multidimensional assembly using layer-by-layer deposition for synchronized cardiac macro tissues.

作者信息

Jang Yongjun, Jung Da Jung, Choi Seung-Cheol, Lim Do-Sun, Kim Jong-Hoon, Jeoung Gi Seok, Kim Jongseong, Park Yongdoo

机构信息

Department of Biomedical Sciences, College of Medicine, Korea University Seoul Korea

Biomedical Engineering Research Center, Asan Institute for Life Sciences, Asan Medical Center Seoul Korea

出版信息

RSC Adv. 2020 May 18;10(32):18806-18815. doi: 10.1039/d0ra01577f. eCollection 2020 May 14.

Abstract

The fabrication of biomimetic structures for tissues and organs is emerging in the fields of biomedical engineering and precision medicine. While current progress in biomedical research provides a number of biofabrication methods, the construction of multi-dimensional cardiac tissue is highly challenging due to difficulties in the maturation and synchronization of cardiomyocytes (CMs) in conjunction with other types of cells, such as myofibroblasts and endothelial cells. Here, we show a simple fabrication methodology to construct multi-dimensional cardiac macro tissue (mCMT) by layer-by-layer (LBL) deposition of cells on micro patterned PDMS. mCMTs formed by LBL deposition of pluripotent stem cell (PSC)-derived cardiomyocytes and cardiac fibroblasts formed 3D patterned structures with synchronized beating characteristics. We also demonstrate that cardiac maturation factors such as the gene expression of MLC2v and cTNI and formation of sarcomeres in mCMTs were significantly enhanced by LBL deposition and growth factors during the maturation process. Fabrication of matured mCMTs with synchronized beating enables providing an efficient platform for evaluating the efficacy and toxicity of drug candidates. These results have important implications because mCMTs are applicable to diverse studies and drug screening methods that require tissue-like structures and functions in a physiological environment.

摘要

用于组织和器官的仿生结构制造正在生物医学工程和精准医学领域兴起。虽然生物医学研究的当前进展提供了多种生物制造方法,但由于心肌细胞(CMs)与其他类型细胞(如肌成纤维细胞和内皮细胞)的成熟和同步存在困难,构建多维心脏组织极具挑战性。在此,我们展示了一种简单的制造方法,通过在微图案化的聚二甲基硅氧烷(PDMS)上逐层(LBL)沉积细胞来构建多维心脏宏观组织(mCMT)。由多能干细胞(PSC)衍生的心肌细胞和心脏成纤维细胞通过LBL沉积形成的mCMT形成了具有同步跳动特征的3D图案化结构。我们还证明,在成熟过程中,LBL沉积和生长因子显著增强了mCMT中诸如MLC2v和cTNI的基因表达以及肌节形成等心脏成熟因子。制造具有同步跳动的成熟mCMT能够为评估候选药物的疗效和毒性提供一个高效平台。这些结果具有重要意义,因为mCMT适用于多种需要在生理环境中具有组织样结构和功能的研究及药物筛选方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7285/9122566/7e6c9a6c24c1/d0ra01577f-f1.jpg

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