The biogenesis of lysosomes and lysosome-related organelles

JP Luzio, Y Hackmann… - Cold Spring …, 2014 - cshperspectives.cshlp.org
Lysosomes were once considered the end point of endocytosis, simply used for
macromolecule degradation. They are now recognized to be dynamic organelles, able to …

[HTML][HTML] β-Coronaviruses use lysosomes for egress instead of the biosynthetic secretory pathway

S Ghosh, TA Dellibovi-Ragheb, A Kerviel, E Pak, Q Qiu… - Cell, 2020 - cell.com
Summary β-Coronaviruses are a family of positive-strand enveloped RNA viruses that
includes the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Much is …

[HTML][HTML] Protein sorting from endosomes to the TGN

DP Buser, A Spang - Frontiers in Cell and Developmental Biology, 2023 - frontiersin.org
Retrograde transport from endosomes to the trans-Golgi network is essential for recycling of
protein and lipid cargoes to counterbalance anterograde membrane traffic. Protein cargo …

Amyloid precursor protein products concentrate in a subset of exosomes specifically endocytosed by neurons

K Laulagnier, C Javalet, FJ Hemming, M Chivet… - Cellular and molecular …, 2018 - Springer
Amyloid beta peptide (Aβ), the main component of senile plaques of Alzheimer's disease
brains, is produced by sequential cleavage of amyloid precursor protein (APP) and of its C …

MicroRNAs are exported from malignant cells in customized particles

J Palma, SC Yaddanapudi, L Pigati… - Nucleic acids …, 2012 - academic.oup.com
MicroRNAs (miRNAs) are released from cells in association with proteins or microvesicles.
We previously reported that malignant transformation changes the assortment of released …

[HTML][HTML] Loss of Christianson syndrome Na+/H+ exchanger 6 (NHE6) causes abnormal endosome maturation and trafficking underlying lysosome dysfunction in …

MF Pescosolido, Q Ouyang, JS Liu… - Journal of …, 2021 - Soc Neuroscience
Loss-of-function mutations in endosomal Na+/H+ exchanger 6 (NHE6) cause the X-linked
neurologic disorder Christianson syndrome. Patients exhibit symptoms associated with both …

Mutant huntingtin is secreted via a late endosomal/lysosomal unconventional secretory pathway

K Trajkovic, H Jeong, D Krainc - Journal of Neuroscience, 2017 - Soc Neuroscience
Huntington9s disease (HD) is an autosomal-dominant neurodegenerative disorder caused
by the expansion of a CAG triplet in the gene encoding for huntingtin (Htt). The resulting …

[HTML][HTML] Starvation and inhibition of lysosomal function increased tau secretion by primary cortical neurons

NV Mohamed, V Plouffe, G Rémillard-Labrosse… - Scientific reports, 2014 - nature.com
Recent studies have demonstrated that human tau can be secreted by neurons and non-
neuronal cells, an event linked to the propagation of tau pathology in the brain. In the …

WASH is required for lysosomal recycling and efficient autophagic and phagocytic digestion

JS King, A Gueho, M Hagedorn… - Molecular biology of …, 2013 - Am Soc Cell Biol
Wiskott-Aldrich syndrome protein and SCAR homologue (WASH) is an important regulator of
vesicle trafficking. By generating actin on the surface of intracellular vesicles, WASH is able …

A complete Rab screening reveals novel insights in Weibel–Palade body exocytosis

S Zografou, D Basagiannis, A Papafotika… - Journal of cell …, 2012 - journals.biologists.com
Summary Weibel–Palade bodies (WPBs) are endothelial-cell-specific organelles that, upon
fusion with the plasma membrane, release cargo molecules that are essential in blood …