Frontier Science Center for Synthetic Biology, Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology , Tianjin University , Tianjin 300350 , People's Republic of China.
College of Chemistry, Research Center for Analytical Sciences, Tianjin Key Laboratory of Molecular Recognition and Biosensing, and State Key Laboratory of Medicinal Chemical Biology , Nankai University , Tianjin 300071 , People's Republic of China.
J Am Chem Soc. 2020 Feb 19;142(7):3422-3429. doi: 10.1021/jacs.9b11001. Epub 2020 Jan 9.
Stem cells have been widely studied in cell biology and utilized in cell-based therapies, and fishing stem cells from marrow is highly challenging due to the ultralow content. Herein, a physically cross-linked DNA network-based cell fishing strategy is reported, achieving efficient capture, 3D envelop, and enzyme-triggered release of bone marrow mesenchymal stem cells (BMSCs). DNA network is constructed via a double rolling circle amplification method and through the intertwining and self-assembly of two strands of ultralong DNA chains. DNA-chain-1 containing aptamer sequences ensures specific anchor with BMSCs from marrow. Hybridization between DNA-chain-1 and DNA-chain-2 enables the cross-link of cell-anchored DNA chains to form a 3D network, thus realizing cell envelop and separation. DNA network creates a favorable microenvironment for 3D cell culture, and remarkably the physically cross-linked DNA network shows no damage to cells. DNA network is digested by nuclease, realizing the deconstruction from DNA network to fragments, and achieving enzyme-triggered cell release; after release, the activity of cells is well maintained. The strategy provides a powerful and effective method for fishing stem cells from tens of thousands of nontarget cells.
干细胞在细胞生物学中得到了广泛的研究,并被应用于基于细胞的治疗中,由于含量极低,从骨髓中提取干细胞极具挑战性。本文报道了一种基于物理交联 DNA 网络的细胞捕捞策略,实现了对骨髓间充质干细胞(BMSCs)的高效捕获、三维包封和酶触发释放。DNA 网络是通过双滚环扩增方法构建的,通过两条超长 DNA 链的缠绕和自组装而成。含适体序列的 DNA 链-1 确保与骨髓中的 BMSCs 特异性锚定。DNA 链-1 和 DNA 链-2 之间的杂交使细胞锚定的 DNA 链交联形成 3D 网络,从而实现细胞包封和分离。DNA 网络为 3D 细胞培养创造了有利的微环境,并且物理交联的 DNA 网络对细胞没有损伤。DNA 网络被核酸酶消化,实现从 DNA 网络到碎片的解构,并实现酶触发的细胞释放;释放后,细胞的活性得到很好的保持。该策略为从数万非目标细胞中提取干细胞提供了一种强大而有效的方法。