A Novel Fluorogenic Probe Reveals Lipid Droplet Dynamics in ME/CFS Fibroblasts

Author:

Ding Siyang1ORCID,Sanislav Oana2ORCID,Missailidis Daniel2ORCID,Allan Claire Yvonne2ORCID,Owyong Tze Cin1ORCID,Wu Ming‐Yu3,Chen Sijie3,Fisher Paul Robert2,Annesley Sarah Jane2ORCID,Hong Yuning1ORCID

Affiliation:

1. Department of Biochemistry and Chemistry La Trobe Institute for Molecular Science La Trobe University Melbourne VIC 3086 Australia

2. Department of Microbiology Anatomy Physiology and Pharmacology School of Agriculture, Biomedicine and Environment La Trobe University Melbourne VIC 3086 Australia

3. School of Life Sciences The Chinese University of Hong Kong Hong Kong China

Abstract

AbstractLipid droplets (LDs) are dynamic cellular organelles that play an essential role in lipid metabolism and storage. LD dysregulation has been implicated in various diseases. However, investigations into the cellular LD dynamics under disease conditions have been rarely reported, possibly due to the absence of high performing LD imaging agents. Here a novel fluorogenic probe, AM‐QTPA, is reported for specific LD imaging. AM‐QTPA demonstrates viscosity sensitivity and aggregation‐induced emission enhancement characteristics. It is live cell permeable and can specifically light up LDs in cells, with low background noise and superior signals that can be quantified. After validation in cell model with LD accumulation induced by oleic acid treatment, AM‐QTPA is applied in a small proof‐of‐concept number of human fibroblast samples derived from people diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), a complex and debilitating disease with unknown cause. The results indicate the presence of larger but fewer LDs in ME/CFS fibroblasts compared to the healthy counterparts, accompanying with frequent LD‐mitochondria contacts, suggesting potential upregulation of lipolysis in ME/CFS connective tissue like fibroblasts. Overall, AM‐QTPA provides new understanding of the anomalous LD dynamics in disease status, which, potentially, will facilitate in‐depth investigation of the pathogenesis of ME/CFS.

Funder

ME Research UK

Australian Research Council

Publisher

Wiley

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