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Yeast is a powerful model organism for dissecting the temporal stages and choreography of the complex protein machinery during endocytosis. The only known mechanism for endocytosis in yeast is clathrin-mediated endocytosis, even though clathrin-independent endocytic pathways have been described in other eukaryotes. Here, we provide evidence for a clathrin-independent endocytic pathway in yeast. In cells lacking the clathrin-binding adaptor proteins Ent1, Ent2, Yap1801, and Yap1802, we identify a second endocytic pathway that depends on the GTPase Rho1, the downstream formin Bni1, and the Bni1 cofactors Bud6 and Spa2. This second pathway does not require components of the better-studied endocytic pathway, including clathrin and Arp2/3 complex activators. Thus, our results reveal the existence of a second pathway for endocytosis in yeast, which suggests similarities with the RhoA-dependent endocytic pathways of mammalian cells.
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http://dx.doi.org/10.1083/jcb.201104045 | DOI Listing |
J Cell Biol
November 2025
Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.
Two major protein recycling pathways have emerged as key regulators of enduring forms of synaptic plasticity, such as long-term potentiation (LTP), yet how these pathways are recruited during plasticity is unknown. Phosphatidylinositol-3-phosphate (PI(3)P) is a key regulator of endosomal trafficking and alterations in this lipid have been linked to neurodegeneration. Here, using primary hippocampal neurons, we demonstrate dynamic PI(3)P synthesis during chemical induction of LTP (cLTP), which drives coordinate recruitment of the SNX17-Retriever and SNX27-Retromer pathways to endosomes and synaptic sites.
View Article and Find Full Text PDFFront Immunol
September 2025
College of Animal Science and Technology, Guangxi University, Nanning, Guangxi, China.
Introduction: Segmented filamentous bacteria (SFB) colonization dynamics are crucial for host immune regulation. Given this, the present study specifically examined the functions of SFB flagellin in bacterial adhesion, cellular internalization, and immune modulation.
Methods: and were engineered to express murine and rat SFB flagellin genes.
Mucosal Immunol
September 2025
Institute for Stem Cell Science and Regenerative Medicine (BRIC-inStem), GKVK-Post, Bellary Road, Bengaluru 560065, India. Electronic address:
Epithelial linings at mucosal sites act in concert with resident immune cells to direct host defense. The epithelial lining of the urethra is an understudied mucosal barrier with emerging roles in antimicrobial defense during urinary tract infections. Here, we present a comprehensive cellular atlas of the adult female mouse urethra, focusing on epithelial and resident immune cells.
View Article and Find Full Text PDFJ Med Chem
September 2025
Department of Neurology, Center for Membrane Receptor and Brain Medicine, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu 322000, Zhejiang, China.
Lysosome-targeting chimeras (LYTACs) have expanded the scope of targeted protein degradation (TPD) by enabling the selective removal of extracellular proteins that are inaccessible to proteasome-dependent strategies. This Perspective examines small-molecule and peptide ligands that interact with several representative lysosome-shuttling receptors and analyzes their structural characteristics, binding mechanisms, and therapeutic implications. We also investigate emerging efforts to exploit noncanonical endocytic pathways mediated by lysosomal membrane proteins, glycosylphosphatidylinositol (GPI)-anchored receptors, lectin receptors, solute carriers, integrins, and GPCRs for LYTAC development.
View Article and Find Full Text PDFSci Rep
August 2025
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.
The ease with which microRNA inhibitors (antimiRs) can be delivered varies with the intended target cell type and tissue. AntimiRs are of interest as potential therapeutics for kidney conditions, including ischaemia-reperfusion injury in transplantation. During ex-situ human kidney perfusion, antimiRs are delivered to the proximal tubule epithelium without the use of transfection reagents by an endocytic process.
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