Publications by authors named "C Heus"

Intestinal stem cells (ISCs) face the challenge of integrating metabolic demands with unique regenerative functions. Studies have shown an intricate interplay between metabolism and stem cell capacity; however, it is still not understood how this process is regulated. Combining ribosome profiling and CRISPR screening in intestinal organoids, we identify the nascent polypeptide-associated complex (NAC) as a key mediator of this process.

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Article Synopsis
  • LIMP-2, or SCARB2, is a key lysosomal membrane protein involved in various functions like acting as a virus receptor, aiding in enzyme targeting, and transporting lipids such as phospholipids and cholesterol.
  • Recent research indicates that LIMP-2 might play a role in the contact points between lysosomes and the endoplasmic reticulum (ER) by interacting with the proteins STARD3 and VAPB.
  • The study suggests that LIMP-2 could help facilitate cholesterol transport from lysosomes to the ER, highlighting its potential role in lipid trafficking and inter-organelle communication.
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Background: In general abdominal surgery, the ratio of fat to muscle mass, or body composition measures, shows a stronger association with complications than body mass index. These studies include male and female patients. Women have a different body composition than men.

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Elucidating the 3D nanoscale structure of tissues and cells is essential for understanding the complexity of biological processes. Electron microscopy (EM) offers the resolution needed for reliable interpretation, but the limited throughput of electron microscopes has hindered its ability to effectively image large volumes. We report a workflow for volume EM with FAST-EM, a novel multibeam scanning transmission electron microscope that speeds up acquisition by scanning the sample in parallel with 64 electron beams.

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The multisubunit HOPS tethering complex is a well-established regulator of lysosome fusion with late endosomes and autophagosomes. However, the role of the HOPS complex in other stages of endo-lysosomal trafficking is not well understood. To address this, we made HeLa cells knocked out for the HOPS-specific subunits Vps39 or Vps41, or the HOPS-CORVET-core subunits Vps18 or Vps11.

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