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An encoded viral micropatch for multiplex cell-based assays through localized gene delivery.通过局部基因传递对多路基于细胞的测定进行编码病毒微贴剂。
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Liquid-capped encoded microcapsules for multiplex assays.用于多重分析的液封编码微胶囊。
Lab Chip. 2017 Jan 31;17(3):429-437. doi: 10.1039/c6lc01268j.
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Adhere, Degrade, and Move: The Three-Step Model of Invasion.黏附、降解与迁移:侵袭的三步模型
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Shape-encoded silica microparticles for multiplexed bioassays.用于多重生物测定的形状编码二氧化硅微粒
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Cardiomyocyte-Driven Actuation in Biohybrid Microcylinders.生物杂交微圆柱体中由心肌细胞驱动的促动
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Controlled fabrication of multicompartmental polymeric microparticles by sequential micromolding via surface-tension-induced droplet formation.通过表面张力诱导液滴形成的顺序微成型法可控制备多室聚合物微粒。
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A co-culture device with a tunable stiffness to understand combinatorial cell-cell and cell-matrix interactions.一种具有可调硬度的共培养装置,用于理解组合细胞-细胞和细胞-基质相互作用。
Integr Biol (Camb). 2013 Nov;5(11):1344-54. doi: 10.1039/c3ib40078f. Epub 2013 Sep 24.
9
Microfluidic assay for simultaneous culture of multiple cell types on surfaces or within hydrogels.微流控分析用于在表面或水凝胶中同时培养多种细胞类型。
Nat Protoc. 2012 Jun 7;7(7):1247-59. doi: 10.1038/nprot.2012.051.
10
Controlled synthesis of 3D multi-compartmental particles with centrifuge-based microdroplet formation from a multi-barrelled capillary.基于多筒毛细管的离心微滴形成法可控合成 3D 多腔室颗粒
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用于两种不同基因微米级病毒递送的微粒逐个形状分层组装。

Hierarchical shape-by-shape assembly of microparticles for micrometer-scale viral delivery of two different genes.

作者信息

Lee Daewon, Lee Amos Chungwon, Han Sangkwon, Bae Hyung Jong, Song Seo Woo, Jeong Yunjin, Oh Dong Yoon, Cho Seongkyu, Kim Junhoi, Park Wook, Kwon Sunghoon

机构信息

Interdisciplinary Program for Bioengineering, Seoul National University, Seoul 08826, South Korea.

Department of Electrical and Computer Engineering, Seoul National University, Seoul 08826, South Korea.

出版信息

Biomicrofluidics. 2018 May 4;12(3):031102. doi: 10.1063/1.5030597. eCollection 2018 May.

DOI:10.1063/1.5030597
PMID:29774082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5935507/
Abstract

Understanding tissue engineering using a bottom-up approach has been hindered by technical limitations because no platform can demonstrate the controlled formation of a heterogeneous population of cells in microscale. Here, we demonstrate hierarchical shape-by-shape assembly of virus-laden particles into larger ones to transfect two different genes on the seeded cells. We show that smaller daughter particles with different sizes and shapes can be assembled into the matching indentations of larger parent particles with different sizes and shapes. Then, we transfected a population of cells with two different gene-transfecting viruses, each of which was laden on the parent or daughter particles.

摘要

由于技术限制,采用自下而上的方法理解组织工程一直受到阻碍,因为没有平台能够在微观尺度上展示异质细胞群体的可控形成。在这里,我们展示了将载有病毒的颗粒逐个层次地组装成更大的颗粒,以便在接种的细胞上转染两种不同的基因。我们表明,具有不同大小和形状的较小子颗粒可以组装到具有不同大小和形状的较大母颗粒的匹配凹痕中。然后,我们用两种不同的基因转染病毒转染一群细胞,每种病毒都负载在母颗粒或子颗粒上。