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Printable Handouts
Navigable Slide Index
- Introduction
- Our aims
- What are reactive astrocytes?
- Lysosome
- Membrane fusion
- Astrocytes
- Lysosomes in astrocytes
- Monitoring single vesicle fusion
- Single-vesicle studies in astrocytes
- Reversible fusion: two vesicle size populations in astrocytes
- IFNy induced antigen presenting in astrocytes
- Reactive astrocytes in vitro (1)
- Reactive astrocytes in vitro (2)
- IFNy affects reversible fusion of larger vesicles
- Fusion pore conductance (Gp) increases in IFNγ- treated astrocytes
- Lysosome antigen presention in astrocytes
- Reducing the number of MHCII–positive compartments in IFNγ–activated astrocytes
- Cholesterol
- Fusion pore conductance is reduced by increased vesicle cholesterol
- The effect of cholesterol on fusion pore constriction
- Fusion pore regulation
- Dendritic cells
- Immunotherapy cancer treatment: challenge
- Immunotherapy cancer treatment: problem
- Immunotherapy cancer treatment: potential solution
- Personalized immunohybridoma cell therapy
- Teaching immune cells to respond to cancer cells
- Electrofusion of cells
- Autologous Hybridoma Cells (aHyC) in clinical trials
- Prostate Cancer (PC)
- Tumor volume and activity over time
- The protocol with the main operational steps
- Clinical trial - aHyC clinical responses
- Clinical trial - aHyC immunological responses
- aHyC clinical trial: correlation between survival and change in NK cells
- aHyC clinical trial: affect on patient survival
- aHyC clinical trial: TTNT and dosage
- Conclusions
- The team, collaborators, funding and advisors
- Acknowledgements
Topics Covered
- Lysosome discovery and function
- Reactive astrocytes
- Measuring vesicle fusion
- Lysosomal fusion in astrocytes
- IFN-y induced antigen-presenting in astrocytes
- Fusion pore regulation
- Dendritic cells
- Autologous Hybridoma Cells (aHyC)
- aHyC treatment for prostate cancer
Talk Citation
Zorec, R. (2024, March 31). Dendritic-tumor cell immunohybridomas: from astroglial lysosomal fusion to treating prostate cancer [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/EMDY8877.Export Citation (RIS)
Publication History
Financial Disclosures
- There are no commercial/financial disclosures.
Dendritic-tumor cell immunohybridomas: from astroglial lysosomal fusion to treating prostate cancer
Published on March 31, 2024
38 min
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, everybody. My
name is Robert Zorec.
I will talk about
lysosomal fusion, today,
and lysosomal fusion that we use
to generate a new
treatment for cancer.
0:14
In the next slide, we see that
what our aims are in the lab,
we study single cells.
We study vesicle dynamics,
signaling cell metabolism,
to gain insights into mechanisms
in health and disease
of, of course, diseases.
And try to transform
key medical challenges
into therapies.
We have two translational
directions:
cancer and neurological
indications.
Cancer, I will talk later,
but I just want to mention
that we have developed
this treatment based on
studying lysosomal
fusion in cells.
And then we made cell-based
immunotherapy to treat
prostate cancer,
the treatment now
available for patients already.
The question is, what is
the common denominator
between these two directions?
Neurological indications and
cancer, we see that these are
two common denominators.
In the nervous system,
we don't only have
nerves, neurons,
but also we have
non neuronal cells
that are called neuroglia.
And this neuroglial cells among
them are also astrocytes.
A property known
aerobic glycolysis.
It's a metabolism that is
also common in cancer cells.
The other common denominator,
of course, as I mentioned,
are lysosomes and lysosomes,
especially in
reactive astrocytes
that are linked to cancer.
1:36
Now, in the next slide,
we try to explain what
reactive astrocytes are.
These are astrocytes that
change during a
pathological insult.
They gain morphological
molecular functional changes.
These changes include hallmark,
that is the overexpression
of intermediate filaments.
These are cytoskeletal
elements that,
actually, determine
the shape of cells.
We asked whether vesicles,
lysosomes in this particular
case are remodeled,
their dynamics is remodeled
under different in
vitro conditions.
In other words, we wanted
to actually generate
reactive astrocytes in
laboratory conditions,
in vitro conditions.
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