通过生物正交方法促进和检测细胞与细胞之间的相互作用

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Evelyn Y. Xue, Alan Chun Kit Lee, Kwan T. Chow and Dennis K. P. Ng*, 
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引用次数: 0

摘要

在组织工程和细胞疗法中,通过细胞表面修饰来控制细胞间的相互作用至关重要。为了能够监测细胞间的相互作用,它还能为了解细胞如何相互作用和交流提供有用的信息。我们在此报告一种促进和监测细胞间相互作用的简便生物正交策略。它包括使用马来酰亚胺修饰的四嗪笼型二吡咯烷硼(BODIPY)荧光探针和马来酰亚胺取代的双环[6.1.0]壬-4-炔(BCN),通过马来酰亚胺-硫醇共轭分别修饰巨噬细胞(RAW 264.7)和癌细胞(HT29、HeLa 和 A431)的膜。修饰后,两种细胞通过表面四嗪和 BCN 分子的反电子需求 Diels-Alder 反应发生强烈相互作用。耦合还能破坏四嗪淬灭单元,恢复细胞-细胞界面上 BODIPY 核心的荧光发射,促进吞噬作用。因此,这种方法可以促进和便利细胞间相互作用的检测,使其有可能用于基于巨噬细胞的免疫疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Promotion and Detection of Cell–Cell Interactions through a Bioorthogonal Approach

Promotion and Detection of Cell–Cell Interactions through a Bioorthogonal Approach

Promotion and Detection of Cell–Cell Interactions through a Bioorthogonal Approach

Manipulation of cell–cell interactions via cell surface modification is crucial in tissue engineering and cell-based therapy. To be able to monitor intercellular interactions, it can also provide useful information for understanding how the cells interact and communicate. We report herein a facile bioorthogonal strategy to promote and monitor cell–cell interactions. It involves the use of a maleimide-appended tetrazine-caged boron dipyrromethene (BODIPY)-based fluorescent probe and a maleimide-substituted bicyclo[6.1.0]non-4-yne (BCN) to modify the membrane of macrophage (RAW 264.7) and cancer (HT29, HeLa, and A431) cells, respectively, via maleimide–thiol conjugation. After modification, the two kinds of cells interact strongly through inverse electron-demand Diels–Alder reaction of the surface tetrazine and BCN moieties. The coupling also disrupts the tetrazine quenching unit, restoring the fluorescence emission of the BODIPY core on the cell–cell interface, and promotes phagocytosis. Hence, this approach can promote and facilitate the detection of intercellular interactions, rendering it potentially useful for macrophage-based immunotherapy.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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