ArticleMethods in molecular biology (Clifton, N.J.)2027
Intestinal Organoids Culture in Synthetic Hydrogels.
Article in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Derived from adult intestinal stem cells, organoids form intricate three-dimensional structures that closely mimic the cellular diversity and spatial organization of the human gut epithelium. Patient-derived organoids (PDOs) can recapitulate patient-specific tumor heterogeneity, making them highly valuable for colorectal cancer research and personalized medicine. However, their long-term in vitro culture still depends mainly on animal-derived materials (e.g., Matrigel) with undefined composition, batch variability, and limited tunability. To overcome these limitations, we introduced the use of synthetic peptide-based hydrogels, particularly peptide amphiphiles alone and in combination with extracellular matrix macromolecules, as a reproducible and tunable alternative. Here, we present a protocol for embedding PDOs in synthetic peptide-based hydrogels, and describe how to extract their RNA for transcriptomic analysis. This workflow enables the culture of intestinal PDOs in synthetic peptide-based hydrogels in a reproducible way, preserving key proliferation and differentiation lineage markers characteristic of PDOs.
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