4.7 Article

A near-infrared plasma membrane-specific AIE probe for fluorescence lifetime imaging of phagocytosis

Journal

SCIENCE CHINA-CHEMISTRY
Volume 65, Issue 5, Pages 979-988

Publisher

SCIENCE PRESS
DOI: 10.1007/s11426-021-1199-6

Keywords

fluorescence lifetime imaging; phagocytosis; plasma membrane; aggregation-induced emission; near-infrared

Funding

  1. Ming Wai Lau Centre for Reparative Medicine, Karolinska Institutet
  2. National Natural Science Foundation of China [22177094, 21708030]
  3. Applied Basic Research of Sichuan Province [2021YJ0397]
  4. Fundamental Research Funds for the Central University [2682021ZTPY039]

Ask authors/readers for more resources

This study developed a near-infrared fluorescent probe named TBTCP for real-time imaging of phagocytosis. TBTCP could selectively label the cell plasma membrane and report the cell membrane statuses and macrophage phagocytosis through fluorescence lifetime changes. It provides a functional tool to study phagocytic function-related diseases.
Phagocytosis is a biological process that plays a key role in host defense and tissue homeostasis. Efficient approaches for realtime imaging of phagocytosis are highly desired but limited. Herein, an AIE-active near-infrared fluorescent probe, named TBTCP, was developed for fluorescence lifetime imaging of phagocytosis. TBTCP could selectively label the cell plasma membrane with fast staining, wash-free process, high signal-to-background ratio, and excellent photostability. Cellular membrane statuses under different osmolarities as well as macrophage phagocytosis of bacteria or large silica particles in early stages could be reported by the fluorescence lifetime changes of TBTCP. Compared with current fluorescence imaging methods, which target the bioenvironmental changes in the late phagocytosis stage, this approach detects the changes in the cell membrane, thus giving a faster response to phagocytosis. This article provides a functional tool to report the phagocytic dynamics of macrophages which may greatly contribute to the studies of phagocytic function-related diseases.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available