Human organ chip models demonstrate FRC-driven HEV differentiation, immune recruitment, and cancer-induced disruption, with FRCs promoting HEV marker expression and structural features.
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Moving in bioRxiv, Blood, Cancer Research, Cell Reports, EMBO Journal, Environmental pollution, Nature Biotechnology and Nature Cell Biology.
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Human organ chip models demonstrate FRC-driven HEV differentiation, immune recruitment, and cancer-induced disruption, with FRCs promoting HEV marker expression and structural features.
A single-chain antibody derivative of TS2/16 enhances gastrointestinal organoid yield up to fivefold in Matrigel and six- to sevenfold in collagen I hydrogels.
P-selectin marks early functional heterogeneity in aging hematopoietic stem cells, with high expression linked to increased DNA damage and myeloid bias in humans and mice.
Endothelial cell-intrinsic NOD2 signaling is essential for T cell recruitment and immune memory formation in the intestine, with NOD2 driving effector and memory T cell accumulation.
De novo E-cadherin/catenin complex formation at the basal epithelial surface enables force transmission and efficient apoptotic cell clearance in zebrafish and mice.
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