Registration for a live webinar on 'Precision medicine treatment for anticancer drug resistance' is now open.
See webinar detailsWe noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Diabetes
- How can we use cell therapy for diabetes?
- Types of stem cells
- Pluripotent Stem Cells (PSCs)
- How could stem cells be used for diabetes?
- Diabetes in a dish
- iPSCs derived from a patient with diabetes
- iPSC characterization
- Insulin resistance & monogenic diabetes models
- Generation of pancreatic cells for cell therapy & disease modeling
- First clinical trial using encapsulated hESC-derived pancreatic progenitors for T1D patients
- First clinical trial using stem cell-derived insulin producing pancreatic islets T1D treatment
- Genes associated with diabetes in pancreatic beta cells
- An example of our work
- iPSC-derived pancreatic islet organoids
- Studying the relationship between psoriasis and insulin resistance using patient-specific iPSCs
- The conclusion of our work
- Deletion of FOXA2 in monogenic diabetes
- FOXA2 deficiency and pancreatic development
- FOXA2 in liver development
- Effect of FOXA2 loss on the development of iPSC-derived hepatocytes
- Absence of FOXA2 induces ER stress
- Lack of FOXA2 increases apoptosis in HP and increases proliferation in MH
- Loss of FOXA2 impairs functions of iPSC-derived hepatocytes
- Improvement in hepatic development and functionality upon FOXA2 overexpression
- Hepatocyte model
- Conclusion
- Acknowledgement
Topics Covered
- Monogenic diabetes
- Pluripotent Stem Cells (PSCs)
- iPSCs derived from a patient with diabetes
- Generation of pancreatic cells for cell therapy
- Clinical trial using encapsulated hESC-derived pancreatic progenitors
- Clinical trial using stem cell-derived insulin-producing pancreatic islets
- Psoriasis and insulin resistance
- FOXA2 in liver development
- Hepatocyte model
Talk Citation
Abdelalim, E.M. (2023, September 28). Human pluripotent stem cells as a platform for precision medicine in diabetes [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/RGCN1015.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Essam M. Abdelalim has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Human pluripotent stem cells as a platform for precision medicine in diabetes
Published on September 28, 2023
52 min
A selection of talks on Immunology
Transcript
Please wait while the transcript is being prepared...
0:00
Hi, I'm Essam Abdelalim,
senior scientist at
Qatar Biomedical Research
Institute and associate
professor at College of
Health and Life Sciences
at HBKU University,
Qatar Foundation, Qatar.
Today I'm going to talk about
human pluripotent stem cells as
a platform for precision
medicine in diabetes.
0:25
Diabetes regardless of
the type of diabetes,
we know that the
problem in case of
diabetes is pancreatic
beta cells which
exist in the endocrine pancreas,
those cells secrete insulin.
We have different
types of diabetes.
We know about type
one and type two
that are the most common
types of diabetes.
Type one represent around 5%
of diabetic patients suffer
from type one and mainly
happened during early age,
mainly in children.
In case of type two,
which represent the most
common form of diabetes.
More than 90% of patients
suffer from type two,
which is mainly genetic.
Mainly happened during,
after 30 or 40 years old.
The cell type, it's monogenic,
it's due to defect in
the single gene and they
represent around or
less than 2% worldwide.
The fourth one is called
gestational diabetes,
or temporary, and
disappear after pregnancy.
To be able to use stem cells
for a different
type of diabetes,
we need to understand what are
the types of cells involved
within an age problem.
In case of type one,
patients suffer from or
develop has a problem
in auto-immune defect,
which is his immune cells or
her immune cells attack the
pancreas to kill beta cells.
The patient loose all beta
cells or most of beta cells,
and this will lead to there is
no insulin secretion in response
to different concentration
of glucose in the blood.
The second type is
totally different.
It has nothing to do
with the immune system,
it is mainly genetic and
the patients suffer from
something called the
insular resistance
in the tissues
several years before the
development of the disease.
This insular resistance happen
mainly in skeletal muscle,
liver cells, and adipose tissue.
Insular resistance there
those tissues that mainly use
the glucose from the blood
or store glucose from the blood,
cannot use stored glucose
because of insulin.
They cannot use insulin which
is secreted from the pancreas.
Then the pancreas start to see
that high level of
glucose in the blood and
beta cells starts to secrete
more and more insulin and
become dysfunctional
with a time.
Insular resistant
mainly happened
like even 10 or more than 10,
15, 20 years before the
development of disease.
The cell type it's monogenic,
as I mentioned, it's a problem.
It's one single gene
defect, mutation or defect.
Here, what happened it
depends on the type of gene
or the name of the gene.
If the gene transcription
factor involved
in the development of the
pancreatic beta cells.
Maybe the patients suffer from
developmental defect
in the beta which
secrete insulin other types
of genes may lead to
beta cell dysfunction.
And maybe also other
type everything is okay
but impairment in
insulin secretion
that you have beta cells,
everything is normal
but insulin is not
secreted from the beta cells and
also in some cases
we see patients
they don't have even
pancreas was called
pancreatic hypoplasia or
agenesis due to defect in one
gene. All of different types
of diabetes can lead
to complications
as all of us know.
How we can use
stem cells or cell therapy
for 2, 3 diabetes?
This is what we'll know.
Hide