Brain development week 5 Flashcards
Explain the development of the neural tube.
What is closure of the neural tube called? Where does closure of the neural tube begin?
In what direction does the neural tube close?
What does the neural tube develop into? What does its cavity become?
Neural tube development (A) begins with an inductive influence of the underlying mesoderm & notochord on the overlying ectoderm resulting in the formation of a neuroectodermal neural plate. This is followed by development of a neural groove and folding of the plate to begin neural tube formation (B). Closure of the neural tube (referred to as neurulation) begins at the mid-region of the embryo during the third week of pregnancy and proceeds to completion during the 4th week closing first at the cranial (anterior) portion of the tube (Day 24) and caudally at posterior neuropore (Day 26). The neural tube develops into virtually all CNS structures. Its cavity becomes the ventricular system.
What occurs after closure of the anterior neuropore? Be specific.
Following closure of the anterior Neuropore there is extensive proliferation of rostral neural tube into 3 primary brain vesicles:
- prosencephalon (forebrain)
- mesencephalon (midbrain)
- rhombencephalon (hindbrain)
Where do neural crest cells develop with respect to the neural plate?
What do neural crest cells develop into?
Neural Crest Cells develop at the lateral edge of the neural plate and are pinched off as the neural tube closes; they then migrate giving rise to sensory (DRG) and autonomic ganglia in the PNS, some cranial nerve ganglia, Schwann and satellite cells.
They also give rise to:
- Pia and arachnoid mater (Leptomeninges)
- Craniofacial mesoderm (which will give rise to muscles and skeletal structures in the head)
- Melanocytes
- Chromaffin (neuroendocrine) cells of adrenal medulla
What is the sulcus limitans?
What do the cellular zones (gray matter) in the future spinal cord organize into? What do these become?
- During week 4 a longitudinal groove called the Sulcus Limitans appears in the lateral wall of the neural tube separating it into a dorsal and ventral half.
- In the future spinal cord, the cellular zones (gray matter) organize into anterior basal plates which become the motor anterior or ventral horns and the posterior alar plates which become the sensory dorsal or posterior horns.
Explain the location of posterior alar plates and anterior basal plates in the brainstem.
Why is the the positions of these plates different in the brainstem?
Where are visceral nuclei located within the brainstem?
- Location of the 4th ventricle and its opening causes the posterior Alar plates to move laterally. Note: Basal Plate derivatives are then in medial locations (GSE, GVE).
- Sulcus limitans still separates all motor and sensory nuclei but explains more lateral location of sensory nuclei (SSA, GSA, GVA) and medial location of motor nuclei
- Visceral nuclei are in intermediate positions
What secondary vesicles are formed from the prosencephalon (forebrain), mesencephalon (midbrain), and rhombencephalon (hindbrain)?
How many secondary vesicles are formed?
What do the central spaces btwn these vesicles become?
Forebrain further develops into the Telencephalon and Diencephalon
Mesenchephalon does not partition further
Hindbrain develops into the Metencephalon and Myelencephalon
Resulting in five secondary vesicles (weeks 5 and 6)
Central Spaces shown on the right are remnants of Neural canal : will develop into the Ventricular system
State what the secondary vesicles develop into.
State what ventricles vesicle is associated with (if applicable).
- The telencephalon further develops into the cerebral cortex, basal ganglia and subcortical white matter. Ventricular space associated with telencephalon are the lateral ventricles.
- The Diencephalon develops into the thalamus, hypothalamus, epithalamus (Pineal gland), subthalamus, retina (retinal ganglion cells) and optic nerve. Ventricular space associated with diencephalon is the Third ventricle.
- The mesenencephalon does not further differentiate into anything (stays as midbrain). The ventricular space associated with the mesencephalon is the cerebral aqueduct.
- The Metencephalon develops into the pons and cerebellum
- The Myelencephalon develops into the medulla oblongata.
- The ventricular space associated with the Hindbrain (eventual pons, cerebellum and medulla) is the Fourth Ventricle.
What flexures occur in the developing neuraxis? What order do they occur in? Where do they occur?
The developing Neural tube bends as these regions develop:
First, the Cranial flexure appears at the Mesenchephalon and the Cervical flexure appears at the Myelencephalon.
This is followed by a Pontine Flexure at the Metencephalon.
What happens to the telencephalic vesicles after formation the the flexures?
Telencephalic vesicles then expand at the rostral limit of the neural tube. Proliferating cortex expands in a C shape that grows over the brainstem and around into the temporal lobe.
What is the surface of the cerebrum and cerebellum like initially? How does this change and why?
The cortex overgrows itself on the lateral surface to cover the ____ ____.
Each cerebral (and cerebellar) hemisphere starts out with a smooth surface and becomes progressively convoluted. This results from massive proliferation and migration of neurons and glial cells.
Greatest amount of this occurs from the 3rd though the 5th fetal months of development. The formation of neuronal connections continues well after birth.
The cortex overgrows itself on the lateral surface to cover the insular cortex. You can see the insula in laboratory by prying open the lateral fissure.
Overgrowth of cerebral cortex around and into the temporal lobe is also manifested in the C-shape of associated structures of the cerebrum and its underlying white matter pathways. What structures does this include?
Overgrowth of cerebral cortex around and into the temporal lobe is also manifested in the C-shape of associated structures of the cerebrum and its underlying white matter pathways. These include the: lateral ventricles (not shown), hippocampus, fornix, corpus callosum, cingulate cortex, and the caudate nucleus (part of basal ganglia; not shown here).
Myelination occurs primarily in the ____ period.
Myelination occurs primarily in the postnatal period.
Explain neurogenesis in the spinal cord.
Neuroepithelial cells divide in the subependymal ventricular zone (A and B in attached pic) and then the neuroblasts emerge from this proliferative region and migrate to an intermediate zone where they then send their axons into an external marginal zone (C). Thus the neurons end up in the central gray matter and the white matter is outside.
Note that neuroblasts are young neurons. They are terminally differentiated which means they are post-mitotic.
Explain neurogenesis of the cortex (cerebrum and cerebellum).
Differentiation of neural tube into future cortex proceeds in an “inside-out” fashion.
Early development of the cerebral cortex: Neuroepithelial cell nuclei undergo cycle of outward and inward migrations in the Ventricular zone (Vz) as they progress through their cell cycle.
Terminal division occurs in the ventricular zone and then neuroblasts migrate from there on radial glia scaffolding to outer regions of the cortex. Cellular gray matter is located on the external surface of cerebral (and cerebellar) cortex and white matter is located inside. Note: Neuroblasts migrate on stationary radial glia cells. radial glial cells send out processes for Neuroblasts to migrate on (see attached pic).
Where are “older” neurons located in the cortex with respect to “newer” neurons?
Later development of the cerebral cortex: Inner cellular layers (1) are formed first, and progressively more superficial layers (2, 3) are formed later. Thus, youngest neurons are in the outer gray layers. Then neurons send their processes inward to create subcortical white matter (which is more deeply located).
What is spina bifida occulta?
What is another name for spina bifida occulta?
What is it typically associated with?
Spina Bifida Occulta (myelocele): is a defect in the vertebral arches that is covered by skin and does not involve the underlying meninges and neural tissue; typically associated with a tuft of hair and/or dimpling of skin in lumbosacral region
What is meningocele?
What is meningomyelocele? What are the results of this type of spina bifida?
What does it mean for the pt to have meningomyelocele at a lower level of the spinal cord (vs a higher one)?
a) Spina bifida with meningocele: a defect where only the meninges protrude through the bony defect.
b) Spina bifida with meningomyelocele: a defect where the spinal cord and/or spinal nerves (e.g. caudal equina) and meninges protrude through the bony defect. These are not covered by skin but have a dural sac filled with CSF and nervous tissue. Flaccid paralysis and sensory loss occurs below the level of the lesion like that which occurs in spinal cord injuries. Bowel and bladder dysfunction are common. The lower the level of the lesion, the less muscular paralysis; therefore increased capacity to walk with less assistive devices and bracing.
see pg 409 of first aid (2013)
What is anencephaly?
Anencephaly: failure of the cephalic part of the neural tube (anterior neuropore) to close. As a result the skull does not close leaving the malformed brain exposed. This condition is incompatible with life.
Which type of Arnold-Chiari malformation is most common?
When may Type 1 Arnold-Chiari malformations be detected? What are the 2 defects that may occur that may lead to detection?
What is a common treatment for this?
Type 1: most common; usually asymptomatic in children and may go undetected until early adult life when the herniation can compress the cord and/or produce upper cervical cord defects such as Syringobulbia and/or Syringomyelia (syrinx or cavitation/cyst in medulla and spinal cord, respectively).
syrinx: fluid filled cavities
cavitation: formation of cavities
Once symptomatic onset occurs, a common treatment is decompression surgery, in which the lamina of the first and sometimes the second and third cervical vertebrae and part of the occipital bone are removed to relieve pressure.
What is type 2 Arnold-Chiari malformation? What is it asscoiated with?
What disease does this type of malformation occur in 90% of its cases?
Arnold-Chiari Malformations Type II: Cerebellar hypoplasia and elongation with caudal displacement of the cerebellum and caudal brainstem through the foramen magnum and associated noncommunicating (obstructive) hydrocephalus; occurs in 90% of cases of meningomyelocele.
What is holoprosencephaly?
What is holoprosencephaly associated with?
What is the severe form associated with?
In what mutations is holoprosencepaly seen in?
Holoprosencephaly: a spectrum of malformations resulting from partial or complete failure of prosencephalon to separate into the paired telencephalon vesicles and the diencephalon (relatively common but incompatible with life); is associated with severe craniofacial anomalies. In severe cases associated with single midline eye (cyclops) with a rudimentary, non-functioning nose (proboscis) above it.
Disorder seen in Sonic Hedgehog (SHH) gene mutations and Patau Syndrome: Trisomy 13
Attached is a brain from newborn with slightly less severe form of holoprosencephaly. Cortical tissue is present along midline, a single lateral ventricle is seen and the diencephalon is fused into single structure; there is complete agenesis of corpus callosum.
What is agenesis of the corpus callosum?
What are the clinical features/developmental outcomes?
What are the causes?
Agenesis of the corpus callosum: part or all of the corpus callosum is absent. A heterogeneous disorder with variable expression and a wide spectrum of clinical features and developmental outcomes. Behavioral characteristics therefore range from severe cognitive impairment and significant neurological abnormalities to the apparently asymptomatic adult with normal intelligence. Results from many different type of gene defects, chromosomal abnormalities and environmental toxins (e.g. Alcohol-FAS)
What are gray matter heterotopias? What are they caused by?
What do individuals with this disease typically have?
Gray matter heterotopias: malformation of cortical development in which clusters of gray matter (depicted in arrows below) are located in abnormal areas due to improper migration of cells during development. Individuals typically have seizures and various neurological deficits depending on degree and location of heterotopias.
What is lissencephaly?
What is it caused by? What disorders are commonly associated with lissencephaly?
What are the effects on individuals with this?
Lissencephaly: smooth brain where cortex does not develop gyri and sulci. A neuronal migration disorder from genetic defects and frequently associated with callosal agenesis and heterotopias as well. Frequently children have global developmental delays (including intellectual disability) and seizure disorders.
What is Dandy Walker Syndrome? State what it is characterized by.
What are the consequences of this syndrome?
Dandy Walker Syndrome: A spectrum of disorders characterized by agenesis of the cerebellar vermis and possibly the corpus callosum; the posterior cranial fossa may be abnormally large. The foramina of Luschka and Magendie in the 4th ventricle fail to open and frequently develop cysts resulting in dilation of the 4th ventricle and non-communicating hydrocephalus. Associated with developmental delays, coordination deficits, and cognitive impairment.
