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定义调节黏附动力学的谱系特异性膜流动性特征。

Defining Lineage-Specific Membrane Fluidity Signatures that Regulate Adhesion Kinetics.

机构信息

Institute of Research, Tokyo Medical and Dental University (TMDU), 15-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan; Department of Regenerative Medicine, Yokohama City University Graduate School of Medicine, Kanazawa-ku 3-9, Yokohama, Kanagawa 236-0004, Japan.

Department of Regenerative Medicine, Yokohama City University Graduate School of Medicine, Kanazawa-ku 3-9, Yokohama, Kanagawa 236-0004, Japan.

出版信息

Stem Cell Reports. 2018 Oct 9;11(4):852-860. doi: 10.1016/j.stemcr.2018.08.010. Epub 2018 Sep 6.

Abstract

Cellular membrane fluidity is a critical modulator of cell adhesion and migration, prompting us to define the systematic landscape of lineage-specific cellular fluidity throughout differentiation. Here, we have unveiled membrane fluidity landscapes in various lineages ranging from human pluripotency to differentiated progeny: (1) membrane rigidification precedes the exit from pluripotency, (2) membrane composition modulates activin signaling transmission, and (3) signatures are relatively germ layer specific presumably due to unique lipid compositions. By modulating variable lineage-specific fluidity, we developed a label-free "adhesion sorting (AdSort)" method with simple cultural manipulation, effectively eliminating pluripotent stem cells and purifying target population as a result of the over 1,150 of screened conditions combining compounds and matrices. These results underscore the important role of tunable membrane fluidity in influencing stem cell maintenance and differentiation that can be translated into lineage-specific cell purification strategy.

摘要

细胞膜流动性是细胞黏附和迁移的关键调节剂,这促使我们定义整个分化过程中谱系特异性细胞流动性的系统景观。在这里,我们揭示了从人类多能性到分化后代的各种谱系中的膜流动性景观:(1) 膜刚性化先于多能性的退出,(2) 膜成分调节激活素信号转导,(3) 特征相对特定于胚层,可能是由于独特的脂质组成。通过调节可变的谱系特异性流动性,我们开发了一种无标记的“黏附分选(AdSort)”方法,该方法仅通过简单的文化操作即可实现,由于筛选条件组合了化合物和基质,超过 1150 种,因此有效消除了多能干细胞并纯化了目标群体。这些结果强调了可调节的膜流动性在影响干细胞维持和分化中的重要作用,可转化为谱系特异性细胞纯化策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e6/6178887/3e40a74dfca7/fx1.jpg

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