Results 1 to 10 of about 168,690 (311)

Branching Off: New Insight Into Lysosomes as Tubular Organelles [PDF]

open access: yesFrontiers in Cell and Developmental Biology, 2022
Lysosomes are acidic, membrane-bound organelles that play essential roles in cellular quality control, metabolism, and signaling. The lysosomes of a cell are commonly depicted as vesicular organelles.
K. Adam Bohnert, Alyssa E. Johnson
doaj   +2 more sources

Super‐resolution analyzing spatial organization of lysosomes with an organic fluorescent probe

open access: yesExploration, 2022
Lysosomes are multifunctional organelles involved in macromolecule degradation, nutrient sensing, and autophagy. Live imaging has revealed lysosome subpopulations with dynamics and characteristic cellular localization.
Taosheng Huang, Lei Wang, Guanqun Han
exaly   +2 more sources

Switching on lysosomes

open access: yeseLife
The formation of large endolysosomal structures in unfertilized eggs ensures that lysosomes remain dormant before fertilization, and then shift into clean-up mode after the egg-to-embryo transition.
Deepak Adhikari, John Carroll
doaj   +3 more sources

An annotated high-content fluorescence microscopy dataset with Hoechst 33342-stained nuclei and manually labelled outlines

open access: yesData in Brief, 2023
Automated detection of cell nuclei in fluorescence microscopy images is a key task in bioimage analysis. It is essential for most types of microscopy-based high-throughput drug and genomic screening and is often required in smaller scale experiments as ...
Malou Arvidsson   +2 more
doaj   +1 more source

Synaptic Function and Dysfunction in Lysosomal Storage Diseases

open access: yesFrontiers in Cellular Neuroscience, 2021
Lysosomal storage diseases (LSDs) with neurological involvement are inherited genetic diseases of the metabolism characterized by lysosomal dysfunction and the accumulation of undegraded substrates altering glial and neuronal function.
Rima Rebiai   +5 more
doaj   +1 more source

Unusual Presentation of Atypical Infantile Pompe Disease in the Newborn Period with Left Ventricular Hypertrophy [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Pompe disease, also known as glycogen storage disease Type II, is a lysosomal storage disorder caused by α-glucosidase deficiency. In general, the clinical spectrum varies with respect to the age of onset, residual enzyme activity and organ involvement.
Sanjay Kumar, Amit Kumar
doaj   +1 more source

The Coordination of Local Translation, Membranous Organelle Trafficking, and Synaptic Plasticity in Neurons

open access: yesFrontiers in Cell and Developmental Biology, 2021
Neurons are highly complex polarized cells, displaying an extraordinary degree of spatial compartmentalization. At presynaptic and postsynaptic sites, far from the cell body, local protein synthesis is utilized to continually modify the synaptic proteome,
Dipen Rajgor   +2 more
doaj   +1 more source

Lysosome-endosome fusion and lysosome biogenesis [PDF]

open access: yesJournal of Cell Science, 2000
ABSTRACT Recent data both from cell-free experiments and from cultured cells have shown that lysosomes can fuse directly with late endosomes to form a hybrid organelle. This has a led to a hypothesis that dense core lysosomes are in essence storage granules for acid hydrolases and that, when the former fuse with late endosomes, a ...
J P, Luzio   +5 more
openaire   +2 more sources

Lysosomes and lysosome‐related organelles in immune responses

open access: yesFEBS Open Bio, 2022
The catabolic, degradative capacity of the endo‐lysosome system is put to good use in mammalian immune responses as is their recently established status as signaling platforms.
Colin Watts
doaj   +1 more source

P2X7 Receptor Triggers Lysosomal Leakage Through Calcium Mobilization in a Mechanism Dependent on Pannexin-1 Hemichannels

open access: yesFrontiers in Immunology, 2022
The P2X7 receptor is a critical purinergic receptor in immune cells. Its activation was associated with cathepsin release into macrophage cytosol, suggesting its involvement in lysosomal membrane permeabilization (LMP) and leakage.
Stephanie Alexia Cristina Silva Santos   +10 more
doaj   +1 more source

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