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Printable Handouts
Navigable Slide Index
- Introduction
- Two hypotheses
- Barrier mechanisms in the brain
- BBB enriched tight junction molecules
- Tight junction in lateral ventricular choroid plexus
- Barrier mechanisms in the developing brain
- Transfer of metabolically important molecules
- Oldendorf BUI uptake method
- BBB transport of arginine
- BBB permeability in newborn and adult rabbits
- BUI of amino acids in newborn and adult rats
- Mouse blood-brain barrier transcriptome
- Solute carrier family
- Transport in the developing mouse blood-CSF
- Distribution of GLUT1 in embryonic brain
- GLUT1 in human fetal cerebral blood vessels
- GLUT1 in human fetal choroid plexus
- Developmental expression of MCT1 and MCT2
- Summary of influx mechanisms
- Protein immunostaining in choroid plexus
- Plasma proteins and lipid-insoluble probes
- BDA and albumin labeled P9 Monodelphis
- Effects of plasma protein on CSF protein
- Bidirectional transfer of biotin dextran
- Transport of plasma proteins and dextrans
- Altered expression in the mouse choroid plexus
- Albumin in embryos and adults
- Expression of Sparc/Gypa/Gypc
- Immunocytochemistry of GYPA
- Immunocytochemistry of SPARC
- Model of albumin transport
- Albumin potential as a drug delivery aid
- Efflux mechanisms in the embryo and fetus
- Distribution of brain ABC transporters
- P-glycoprotein of brain microvessels in adult
- P-glycoprotein of human fetal brain
- Role of BCRP in fetal protection
- mRNA in choroid plexus (qPCR)
- BCRP in rat cortex
- BCRP in rat choroid plexus
- BCRP in embryonic and adult rat
- ABC gene expression in cerebral endothelial cells
- ABC gene expression in mouse choroid plexus
- ABC gene expression in adults and embryos
- Transporters in developing choroid plexus
- Further studies
- Practical consequences
- Developmental toxicity of industrial chemicals
- Consequences of prenatal toxin exposure
- Drugs in pregnancy and lactation
- Need for systematic studies
- Exposure to environmental toxins
- Toxicological properties of heavy metals
- Excitotoxic amino acids
- Inflammation during brain development (1)
- Inflammation during brain development (2)
- Short term effect on white matter tract volume
- Long term effect of prolonged inflammation
- Biotin ethylenediamine: adult rat external capsule
- LPS injected in neonatal rat and claudin-5
- Vulnerability of the developing brain summary
- Overall summary
- Acknowledgements
- Reference & reading list
Topics Covered
- The brain develops within a well-defined internal environment
- The properties of this internal environment are determined by transporters in the cellular interfaces between the blood, brain and cerebrospinal fluid
- The transporters are effective because the intercellular spaces between the cells in the interfaces are sealed by tight junctions
- The transporters are both influx and efflux and many are active very early in brain development
- Although brain barrier mechanisms are present very early in development they are vulnerable to pathological conditions e.g. inflammation, which may result in barrier dysfunction and damage to the fragile developing brain
- These mechanisms thus provide protection and a stable internal environment, but some may render the developing brain more vulnerable e. g. inward transport of toxins such as mercury via a normal amino acid transporter
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Talk Citation
Saunders, N. (2014, January 13). Barrier mechanisms in the developing brain: protection or vulnerability? [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/SDSJ2758.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Norman Saunders has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Barrier mechanisms in the developing brain: protection or vulnerability?
A selection of talks on Neurology
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. My name is Norman Saunders.
I run a research laboratory in the University of Melbourne in Australia.
This is the second of 2 talks on barrier mechanisms in the developing brain.
In the first talk I said that I would deal with 2 hypotheses,
which are shown in this next slide.
0:20
The first hypothesis is that the brain develops within a well controlled internal environment
that is determined by mechanisms in brain barrier interfaces.
And the second hypothesis is that disturbance of brain barrier mechanisms in the embryo
may have immediate or long-term consequences for brain development
and may underlie some developmental and adult neurological disorders.
In that first talk I dealt mainly with the first hypothesis.
In this second talk I shall give you additional information,
much of it only recently published, which bears on the notion
that the brain develops within a well controlled internal environment.
I'd like to begin with an update on the information that I gave you in that first talk
about the integrity of tight junctions in blood vessels in the developing brain.
1:06
This slide is a reminder of the main barrier interfaces in the adult and developing brain.
In addition to the morphological evidence outlined in the first talk,
there is now molecular evidence which reinforces the finding
that tight junctions in the blood-brain and blood-CSF barriers
are functionally effective even in the embryo and neonate.
Molecular expression studies of Daneman and his colleagues in Stanford University
have shown that the junctional proteins occludin and numerous claudins
are expressed in postnatal mouse cerebral blood vessels within a few days of birth,
and that's illustrated in the next slide.
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