Single-cell mapping of lipid metabolites using an infrared probe in human-derived model systems.
Yeran BaiCarolina M CamargoStella M K GlasauerRaymond GiffordXinran TianAndrew P LonghiniKenneth S KosikPublished in: Nature communications (2024)
Understanding metabolic heterogeneity is the key to uncovering the underlying mechanisms of metabolic-related diseases. Current metabolic imaging studies suffer from limitations including low resolution and specificity, and the model systems utilized often lack human relevance. Here, we present a single-cell metabolic imaging platform to enable direct imaging of lipid metabolism with high specificity in various human-derived 2D and 3D culture systems. Through the incorporation of an azide-tagged infrared probe, selective detection of newly synthesized lipids in cells and tissue became possible, while simultaneous fluorescence imaging enabled cell-type identification in complex tissues. In proof-of-concept experiments, newly synthesized lipids were directly visualized in human-relevant model systems among different cell types, mutation status, differentiation stages, and over time. We identified upregulated lipid metabolism in progranulin-knockdown human induced pluripotent stem cells and in their differentiated microglia cells. Furthermore, we observed that neurons in brain organoids exhibited a significantly lower lipid metabolism compared to astrocytes.
Keyphrases
- induced pluripotent stem cells
- endothelial cells
- single cell
- high resolution
- fluorescence imaging
- pluripotent stem cells
- induced apoptosis
- gene expression
- high throughput
- rna seq
- stem cells
- ms ms
- brain injury
- cell death
- multiple sclerosis
- spinal cord injury
- bone marrow
- spinal cord
- mass spectrometry
- oxidative stress
- living cells
- drug induced
- sensitive detection
- fluorescent probe