Neuroscience Week 2: Development of the CNS & PNS Flashcards

(119 cards)

1
Q

Neurulation overview

A

Notochord induces overlying ectoderm to develop the neural plate

The neural plate folds into the neural tube and the neural crests are pinched off

the neural tube derives the CNS

the Neural crests derive the PNS + select other cells (e.g. melanocytes)

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2
Q

Notochord

A

Forms the embryonic central axis

Induces neural plate formation

Establishes central column of spine: degenerates to nucleus pulposus

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3
Q

Neurulation day 17

A

early regression of primitive streak and the development of the neural plate

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4
Q

Neurulation Day 18

A

neural plate invaginates to form neural groove that dips centrally

and

the neural folds that peak laterally

and the neural crests are located at the tips of the neural folds

and

somite development in the mesoderm

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5
Q

somites derived from?

A

Paraxial Mesoderm

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6
Q

Somites become

A
  • Sclerotome
  • Myotome
  • Dermatome
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7
Q

Sclerotome becomes

A

bone and cartilage

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8
Q

Myotome becomes

A

skeletal muscle

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9
Q

Dermatome becomes

A

dermis

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10
Q

Neurulation Day 21

A

primitive streak nearly completely regressed

neural groove starts to fully fold to form the neural tube which enters the mesoderm

it closes off in the center first

neural tube is closed and resides in the mesoderm

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11
Q

Neurulation Day 23

A

Much more of the neural tube is closed

the anterior cranial neuropore closes ~ day 24

The posterior caudal neuropore closes ~ day 26

somites form ridges under the ectoderm

neural crest cells above the neural tube (neural crest produce BMP and WNT) signal the neural tube to form the roof plate and bilateral allar plates

the floor plate of the neural tube is signaled by the notochord to form by SHH and signalled to form the bilateral basal plates as well

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12
Q

Gastrulation overview

A
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13
Q

Germ layer derivatives

A
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14
Q

Neurulation Summary

A
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15
Q

Fate map of the early neural plate

A
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16
Q

Fatemap of the early neural tube overview

A
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17
Q

Fate of the notochord

A
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18
Q

Brain vesicle formation Overview

A
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19
Q

Brain Vesicle formation

A

The neural tube differentiates into brain vesicles

The primary brain vesicles have developed by 4 weeks

secondary brain vesicles have developed by 5 weeks

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20
Q

Identify

A
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21
Q

Primary brain vesicles

A

Prosencephalon

Mesencephalon

Rhombencephalon

Neural tube

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22
Q

Secondary brain vesicles

A

Telencephalon

Diencephalon

Mesencephalon

Metencephalon

Myelecephalon

Neural tube

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23
Q

Identify

A
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24
Q

Flexures

A

Cephalic flexure

Cervical flexure

Pontine flexure

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25
Flexure for 4th ventricle
Pontine flexure is 4th ventrical floor
26
Optic vesicle becomes
Optic cup Optic Stalk
27
Optic cup becomes
Retina
28
Optic Stalk becomes
Optic nerve
29
brain vesicle formation at 6 months
Insula remains exposed
30
Cerebral cortex derived from
Telencephalon
31
Thalamic Areas Derived from
Diencephalon
32
Midbrain derived from
Mesencephalon
33
Pons + Cerebellum derived from
Metencephalon
34
Medulla Oblongata derived from
Myelencephalon
35
Spinal cord derived from
Neural tube
36
Regional specification
37
Continued regional specification
38
Neural tube defects
anomalies of neural tube folding 2nd is most common cause of congenital anomaly (2nd to cardiac)
39
Mainstay of neural tube defect prevention
Folic acid supplementation up to 4 mg per day
40
Important diagnostic marker of neural tube defects
Alpha-fetoprotein (AFP) is an important diagnostic marker because it escapes into the amniotic cavity
41
Valproic acid
neural tube teratogen (anti-epileptic drug)
42
Neural Tube Defects: Anencephaly
* acrania (absence of skull) * failure of cerebral hemispheres to develop (forebrain) * angiomatous stroma (undifferentiated neural tissue that mimics appearance of brain is present above the orbits and skull base and is exposed to the environment * infants survive just a few hours and never achieve consciousness
43
Neural Tube Defects:: Encephalocele
herniation of meninges and brain matter associated with hydrocephalus and microcephaly occipital encephalocele a key feature of Meckel-Gruber syndrome
44
Merkel-Gruber Syndrome
autosomal recessive disorder cystic renal dysplasia polydactyly occipital encephalocele
45
cephalocele
herniation of the meninges only without brain matter
46
Neural Tube Defects: Rachischisis , spinal dysraphism
spinal defects
47
Neural Tube Defects: Rachischisis
Spina bifida w/ myeloschisis a failure of spinal cord development spinal cord is flattened along the dorsum of the bodies surface (no neural root plate present) Not a survivable defect
48
Spina Bifida w/ myeloschisis AKA
Myelocele
49
Spina Bifida w/ myeloschisis
Form called rachischisis not survivable
50
Spina Bifida w/ Meningocele AKA
Spina Bifida Cystica
51
Spina Bifida Cystica w/ Meningocele
cyst like meningeal sac protruding through vertebral arch defect neural structures intact and in the right location can experience functional deficits similar to meningomyelocele
52
Spina Bifida w/ Meningomyelocele AKA
Spina Bifida Cystica
53
Spina Bifida w/ Meningomyelocele
displaced meningeal and neural structures often results in paralysis below the lesion allow the spinal cord folds appropriately the displacement results in severe functional deficits
54
Associated syndromes with Spina Bifida Manifesta
Chiari type II malformation - Lumbar meningomyelocele Dandy walker - Spina Bifida
55
Spina Bifida Occulta
no meningeal protrusion but a failure of vertebral arch fusion that is covered in skin can have hairy patch, dimple or birthmark can be a harbinger of a tethered cord syndrome
56
Tethered Cord syndromes
traction damage to the caudal spinal cord e.g. filum terminale thickening or lipoma which commonly cause bladder incontinence
57
Lumbar punctures
58
Neural tube internal organization Basal plates and alar plates fate
Alar plates - Dorsal sensory horns nerve roots Basal plates - ventral motor horns nerve roots
59
Dermatome
axial dermis
60
Myotome
paraspinal and abdominal musculature
61
Sclerotome
spine and posterior basal skull
62
Neural tube zones
* Ventricular * Intermediate * Marginal zone
63
Ventricular zone produces
Ependymal layer
64
Intermediate zone produces
Gray Matter (neurons)
65
Intermediate zone AKA
Mantle zone
66
Marginal Zone Produces
White Matter Glioblasts (Glia)
67
Alar plate and Basal plate
Alar - dorsal horn Basal - Ventral horn
68
Dorsal nerve root ganglion
cluster of pseudounipolar neurons and grows centrally into the alar plate
69
Ventral Nerve Root
grows from the basal plate is a motor root
70
Overview of Development of spinal cord and Nerve Roots
71
Spinal nerve roots
72
Spinal cord inducing centers
73
Forebrain Signaling Centers
74
Neural Crest Cell Differentiation Overview 10 listed
75
Neural Crest Derivatives
* PNS = Glial Cells + Schwann Cells * Meninges: Pia and Arachnoid * Melanocytes * Enteric Nervous System **Cranial** * Pharyngeal Arch Components * Musculoskeletal Structures * Cranial nerves **Trunk and Lumbosacral** * Dorsal Root Ganglia * Sympathetic chain ganglia * Adrenal Medullary Cells * Prevertebral ganglia
76
Neural Crest Cell Migration
77
Neural Crest cells as the 4th germ layer
78
Neural Crest cells and dorsal root and autonomic ganglia
79
Abnormal Development of CNS / PNS
80
Prevention of Neural Tube Defects
81
Failures of anterior Neuropore Closure 2 listed
Anencephaly Encephalocele
82
Anencephaly
83
Encephalocele
84
Caudal Neural Tube Defects
85
Failure of posterior neuropore closure
Spina Bifida Occulta Spina Bifida Cystica (meningocele and meningomyelocele) Spina Bifida w/ myeloschisis
86
Spina Bifida Occulta
87
Spina Bifida Cystica
88
Non-communicating hydrocephalus
89
Chiari Malformations
90
Hydromelia & Syringomyelia
91
Dandy-Walker Syndrome
92
Holoprosencephaly HPE Spectrum
93
Holoprosencephaly Summary
94
Detection and treatment of NTDs
95
Maturation of primary brain divisions
96
Lissencephaly
97
Ulegyria
98
Developmental Reflexes
99
Pyrimidal Tract and myelination
100
APGAR Scoring system for newborns
101
Germinal Matrix Hemorrhage
102
Summary of CNS Developmental Defects/Injuries
103
Neurocutaneous Disorders
104
Neurofibromatosis Type I
105
Neurofibromatosis Type I findings
106
Neurofibromatosis Type II
107
Sturge-Weber Disorder
108
Sturge-Weber Syndrome Findings
109
Tuberous Sclerosis
110
Tuberous Sclerosis Findings
111
Von Hippel-Lindau Syndrome
112
Von Hippel-Lindau Syndrome Findings
113
Summary of Neurocutaneous Disorders
114
dura mater derivative of
mesoderm derivative
115
holoprosencephaly
mainly week 5 failure of midline structures to segregate
116
elevated alfa-feto protein can indicate? & causes of false positives
neural tube defect * miscalculation of gestational age * twins * maternal tumor or liver disease
117
high levels of AchE in Amniotic fluid
can indicate NTD
118
When does the rostral neuropore close?
day 24/25
119
When does the caudal neuropore close?
Day 26/27