Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Lipid droplets (LDs) and lysosomes are crucial for maintaining intracellular homeostasis. But single fluorescent probes (SFPs) capable of simultaneous and discriminative visualizing of two organelles above and their interaction in living cells are still challenging due to the lack of rational design strategies. To break this bottleneck, herein, we develop a reliable strategy based on a pH-sensitive intramolecular spirocyclization. As a proof of concept, an SFP , which possesses a switchable hemicyanine/spiro-oxazine moiety induced by pH, has been designed and synthesized. In acidic environments, the ring-open form exhibits red-shift emission and low logP value, whereas the ring-closed form displays blue-shift emission and high logP value in neutral or basic environments. Thus, the distinct different hydrophilicity/hydrophobicity and absorption/emission properties of these two forms enable targeting LDs and lysosomes simultaneously and discriminatingly. Very importantly, the dynamic process of lipophagy can be directly monitored with . The success of indicated that the spirocyclization strategy is efficient for constructing SFPs to LDs and lysosomes.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.analchem.1c01842DOI Listing

Publication Analysis

Top Keywords

lds lysosomes
12
spirocyclization strategy
8
single fluorescent
8
lipid droplets
8
ph-sensitive spirocyclization
4
strategy constructing
4
constructing single
4
fluorescent probe
4
probe simultaneous
4
simultaneous two-color
4

Similar Publications

Although lipid droplets (LDs) are established as metabolic regulators of iron-dependent ferroptosis in hepatocellular carcinoma (HCC), their biophysical remodeling and spatiotemporal interactions with other organelles during this cell death process have been incompletely characterized. In this study, we developed , a bifunctional molecular probe that combines lipophilicity-guided organelle targeting with viscosity-dependent fluorescence activation while exhibiting ideal spectral orthogonality to commercial fluorescent markers. Using , we detected elevated LD viscosity during erastin-induced ferroptosis and reduced viscosity upon ferrostatin-1-mediated inhibition.

View Article and Find Full Text PDF

HSP90 deficiency promotes cholesteryl ester accumulation in lipid droplets via endocytosis of low-density lipoprotein.

Commun Biol

August 2025

Shanghai Key Laboratory of Metabolic Remodeling and Health, State Key Laboratory of Genetics and Development of Complex Phenotypes, Institute of Metabolism and Integrative Biology, School of Life Sciences, Department of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai, Ch

The size and number of lipid droplets (LDs), as intracellular lipids storage organelles, are closely correlated to lipid metabolism. However, the regulation of lipid metabolism is still unclear. Here, based on changes in three LD phenotypic indicators, including LD number, average LD area, and total LD amount in a cell, we establish an imaging-based high-throughput screen on a compound library.

View Article and Find Full Text PDF

Lipid Droplet Degradation Through Lipophagy in Aurantiochytrium limacinum mh0186.

Mar Biotechnol (NY)

August 2025

Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, 744 Motooka, Nishi-Ku, Fukuoka, 819-0395, Japan.

Autophagy is a cellular recycling process degrading and reusing cytoplasmic components via lysosomes or vacuoles, whereas lipophagy is a specialized form of autophagy that degrades lipid droplets (LDs). Thraustochytrids are heterotrophic marine protists known for high polyunsaturated fatty acid (PUFA) production and as valuable models for lipid metabolism research. In this study, LD degradation in Aurantiochytrium limacinum mh0186 was characterized under glucose-starvation conditions.

View Article and Find Full Text PDF

A series of Nile red derivatives (N1-N3) were synthesized and systematically investigated in terms of their photophysical properties and sub-cellular imaging capabilities. Among them, N1 exhibited dual-channel fluorescence imaging, localizing predominantly in lipid droplets (LDs) under 488 nm excitation and additionally targeting the endoplasmic reticulum (ER). Notably, prolonged light irradiation induced a dynamic shift in N1 localization from the smooth ER to the rough ER, offering a rare chemical tool to distinguish these ER sub-domains.

View Article and Find Full Text PDF

An ethanol-induced loss of the lipid droplet-associated segregase VCP/p97 leads to hepatic steatosis.

J Cell Biol

August 2025

The GI Center for Digestive Diseases, The Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, MN, USA.

The liver stores substantial numbers of neutral lipid organelles termed lipid droplets (LDs) that accumulate within hepatocytes in response to chronic ethanol (EtOH) consumption leading to hepatic steatosis. Mass spectrometry analysis of LDs isolated from EtOH-damaged rat livers revealed a substantial reduction in the valosin-containing protein ATPase (VCP/p97) that acts to remove targeted proteins from cellular membranes for degradation. Experimental disruption of VCP function resulted in an increase in LD content in hepatocytes and mouse livers along with a marked increase in LD-associated hydroxysteroid dehydrogenase (HSD17β13) known to contribute to hepatic steatosis.

View Article and Find Full Text PDF