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
- Table of contents
- Introduction
- The Central Nervous System (CNS)
- CNS borders
- Endothelial Cells (ECs)
- Blood Endothelial Cells (BECs)
- Lymphatic Endothelial Cells (LECs)
- Multiple sclerosis
- Experimental autoimmune encephalomyelitis (EAE)
- The pathophysiology of EAE
- The pathophysiology of EAE: axon demyelination
- Endothelial cells in neuroinflammation
- The CNS borders
- Endothelial cells from the BBB
- T cell migration across the BBB at steady state
- T cell migration across the BBB during EAE
- CD8+ T cells recognize MHCI-CNS antigen
- Endothelial cells from the BBB modulate CNS immune responses
- The meninges: a protective barrier of the CNS
- Effector T cell reactivation in meninges
- Meningeal lymphatic endothelial cells (LECs)
- Meningeal LECs: physiological conditions and EAE
- Meningeal BECs (in the dura)
- Meningeal BECs (in the leptomeninges)
- LECs from the cribriform plate
- LECs from the cribriform plate: during EAE
- Conclusions
- Thank you
Topics Covered
- Endothelial cells as regulators of autoimmune-neuroinflammation
- The central nervous system (CNS)
- The endothelial cells
- Neuroinflammation
- Endothelial cells from the blood brain barrier (BBB)
- Endothelial cells from the meninges
- Lymphatic endothelial cells from the cribriform plate
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Garnier, L. (2024, October 31). Endothelial cells: regulators of autoimmune-neuroinflammation [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/YJWC8325.Export Citation (RIS)
Publication History
Financial Disclosures
- There are no commercial/financial matters to disclose.
Other Talks in the Series: The Immune System - Key Concepts and Questions
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, everyone. I'm
Dr. Laure Garnier,
a Senior Postdoc in
Professor Stephanie Hugues'
Lab in Geneva in Switzerland.
Today, I will talk about the
role of endothelial cells
as regulators of autoimmune
neuroinflammation.
0:18
This lecture will be divided
into different points.
I will introduce what is
the central nervous system,
I will call it CNS,
the endothelial cells,
and neuroinflammation with
a special focus on
multiple sclerosis and
its animal models,
the experimental autoimmune
encephalomyelitis, or EAE.
Then, I will detail
what the function of
endothelial cells from the
blood-brain barrier is,
the meninges, and the
cribriform plate in
neuroinflammation and more
particularly, in EAE.
0:53
For the introduction part,
the central nervous system,
0:57
which I said, I
will call the CNS,
consists of the brain
and the spinal cord.
It receives, processes,
and responds to
information from the body.
The CNS has been
traditionally considered
an immunologically ignored
organ lacking
immunosurveillance.
1:20
This dogma has evolved and
now current knowledge is that
the CNS borders that comprise
the blood-brain barrier or BBB,
the blood-cerebrospinal
fluid barrier or BCSFB,
and the blood meningeal
barrier, BMB,
control immunoregulation
to maintain
neural homeostasis
and tolerance to
CNS antigen and to prevent
neuroinflammation
and resolve damages.
Those barriers are composed of
endothelial cells
so the cells we
are interested in
this topic are,
epithelial cells,
pericytes, and astrocytes.
The anatomic location of
the CNS immune responses
tightly controls immune
cell migration and entry to
the central nervous
system parenchyma
where neurons are located.