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Printable Handouts
Navigable Slide Index
- Introduction
- Traditional view of the lysosome
- Lysosomal functions
- The structure of the lysosome
- Lysosomal function: transcriptionally regulated?
- TFEB regulation of lysosomal gene expression
- TFEB and cellular clearance in diseases
- Lysosomal storage diseases (LSDs)
- TFEB rescues lysosomal vacuolization
- TFEB & clearance through lysosomal exocytosis
- TFEB reduces pathologic lysosomal storage
- Validation of TFEB role in different studies
- Summary 1
- How is TFEB activity regulated?
- Regulation of TFEB subcellular localization
- Starvation induces TFEB nuclear translocation
- Pharmacological inhibition of mTOR kinase
- mTORC1 inhibits TFEB nuclear translocation
- TFEB regulation by phosphorylation
- TFEB (HC)-screening
- An outline of the calcineurin pathway
- Calcineurin & TFEB nuclear translocation
- Calcineurin binds TFEB
- Calcineurin dephosphorylates TFEB
- Calcineurin regulation
- Ca2+ induces TFEB nuclear translocation
- Ca2+, calcineurin & TFEB nuclear translocation
- Depletion of calcineurin
- What activates calcineurin to de-phosphorylate?
- The role of the MCOLN1 gene
- Starvation induces lysosomal Ca2+-release
- MCOLN1 induces TFEB nuclear translocation
- MLIV cells & TFEB nuclear translocation
- Summary 2
- Lysosome: more than a degradative organelle
- Acknowledgements
Topics Covered
- Lysosome as degradative organelle
- Transcriptional regulation of lysosomal and autophagic function
- Promoting clearance through overexpression of TFEB in lysosomal storage disorders
- TFEB regulation by phosphorylation
- Imaging approaches to identify phosphatase regulating TFEB nuclear translocation
- Role of the lysosomal calcium channel TRPML1 in TFEB nuclear translocation
Talk Citation
Medina, D. (2018, October 31). Lysosome: much more than a degradative organelle [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/UTSL2021.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Diego Medina has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: Autophagy and Lysosomal Storage Diseases
Transcript
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0:00
My name is Diego Louis Medina,
Assistant Investigator at
the Telethon Institute of Genetics and Medicine at Pozzuoli, Italy.
The title of my presentation today is, Lysosome: Much More Than a Degradative Organelle.
0:17
The lysosome has been considered for many years as the cells trash can.
An organelle involved in catabolic pathways and not subject to any particular regulation.
0:29
Thus the lysosome is able to degrade a variety of macromolecules
coming from major intracellular pathways, through autophagy and endocytosis.
In addition the lysosome can insert
a very specialized function called lysosomal exocytosis:
a calcium-dependent process involved in
the expelling of lysosomal content outside of the cell.
0:54
The lysosome is a single enclosed organelle that
contains a set of hydrolases, that work in
the acidic environment of the lysosomal lumen, and are
responsible for the catabolic function of this organelle.
The lysosome membrane is rich with highly glycosylated proteins, such as the LAMP proteins
that protect the lysosome and the cell from cell aging.
In addition the lysosomal membrane contains other components, such as
the vesicular proton pump, that generates the acidic environment of the lysosome;
ionic channels that keep ionic homeostasis;
different transporters of lipids,
like MPC proteins or amino acids like LAAT1;
and other transporters for the recycling of the catabolism of
macromolecules; as well as proteins involved in trafficking and fusion of membranes,
like RABs and SNARE proteins.