Project: iPSC-based parenchymal and sinusoidal liver cell mimics for DILI and NAFLD studies (iPSC-LiMic)
2020-10-01 – 2024-09-30
- Abstract
In iPSC-LiMic, we will create functional 3D co-cultures of human iPSC-derived mature hepatocytes and sinusoidal
cells (termed 3D iP-liver mimics) that will serve as a robust model for high-throughput screens for studying drug
toxicity and metabolic diseases. As iPSCs are an inexhaustible source of cells, this will circumvent the variability
observed with primary liver cells. To date, no studies have created iPSC-derived Kupffer cells (KCs) or liver
sinusoidal endothelial cells (LSECs) nor have any studies generated an all-human iPSC derived model containing
hepatocytes, hepatic stellate cells (HSCs), LSECs and KCs. This is in large part due to the lack of knowledge
regarding the phenotype of these cells. It is this scientific knowledge gap that iPSC-LiMic will address.
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- Journal Article
- A1
- open access
Unraveling cell-cell communication with NicheNet by inferring active ligands from transcriptomics data
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- Journal Article
- A1
- open access
Spatially restricted and ontogenically distinct hepatic macrophages are required for tissue repair
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- Journal Article
- A1
- open access
Spotless, a reproducible pipeline for benchmarking cell type deconvolution in spatial transcriptomics
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- Journal Article
- A1
- open access
Spatial proteogenomics reveals distinct and evolutionarily conserved hepatic macrophage niches
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- Journal Article
- A1
- open access
Osteopontin expression identifies a subset of recruited macrophages distinct from Kupffer cells in the fatty liver