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Multicolor Two-Photon Microscopy Imaging of Lipid Droplets and Liver Capsule Macrophages In Vivo
  • Kim, Eun Seo ;
  • Lee, Jeong Mi ;
  • Kwak, Jong Young ;
  • Lee, Hyo Won ;
  • Lee, In Jeong ;
  • Kim, Hwan Myung
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Publication Year
2024-05-28
Publisher
American Chemical Society
Citation
Analytical Chemistry, Vol.96, pp.8467-8473
Mesh Keyword
Chronic nonalcoholic fatty liver diseaseEnergyGreen fluorescent proteinIn-vivoLipid dropletsLiver capsuleMicroscopy imagingMulti-colorsNon-alcoholic fatty liver diseaseTwo photon microscopy
All Science Classification Codes (ASJC)
Analytical Chemistry
Abstract
Lipid droplets (LDs) store energy and supply fatty acids and cholesterol. LDs are a hallmark of chronic nonalcoholic fatty liver disease (NAFLD). Recently, studies have focused on the role of hepatic macrophages in NAFLD. Green fluorescent protein (GFP) is used for labeling the characteristic targets in bioimaging analysis. Cx3cr1-GFP mice are widely used in studying the liver macrophages such as the NAFLD model. Here, we have developed a tool for two-photon microscopic observation to study the interactions between LDs labeled with LD2 and liver capsule macrophages labeled with GFP in vivo. LD2, a small-molecule two-photon excitation fluorescent probe for LDs, exhibits deep-red (700 nm) fluorescence upon excitation at 880 nm, high cell staining ability and photostability, and low cytotoxicity. This probe can clearly observe LDs through two-photon microscopy (TPM) and enables the simultaneous imaging of GFP+ liver capsule macrophages (LCMs) in vivo in the liver capsule of Cx3cr1-GFP mice. In the NAFLD mouse model, Cx3cr1+ LCMs and LDs increased with the progress of fatty liver disease, and spatiotemporal changes in LCMs were observed through intravital 3D TPM images. LD2 will aid in studying the interactions and immunological roles of hepatic macrophages and LDs to better understand NAFLD.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/34201
DOI
https://doi.org/10.1021/acs.analchem.4c00228
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Type
Article
Funding
This study was supported by grants from the National Leading Research Lab Program of the National Research Foundation of Korea (NRF) (NRF-2022R1A2B5B03001607), Centre for Convergence Research of Neurological Disorders (NRF-2019R1A5A2026045), and Basic Science Research Program (2021R1A6A1A10044950). I.J.L. received a grant from the Basic Science Research Capacity Enhancement Project (2021R1A6C103B407). J.Y.K. received a grant from the Korea Basic Science Institute (National Research Facilities and Equipment Center), funded by the Ministry of Education (2019R1A6C1010003).
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Kim, Hwan Myung김환명
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