18 Nervous System Development

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In the following chapters, some of the many structures that make up the brain will be introduced. To begin this discussion, we will identify some of the basic development of the nervous system to understand how different areas of the brain are organized. An extremely simplified view of early development is presented below.

The first stage after fertilization is cleavage, involving a series of synchronized cell divisions. Cells develop and divide together, because embryonic transcription has not yet started, and it’s the maternal transcripts that are being translated. Embryonic cell division becomes asynchronous when embryonic cell division starts, at the blastula stage. Eventually, the zygote develops into a flat layer of cells called the epiblast.

The next step of development, shared across many different animal clades, is gastrulation. During gastrulation, cells rotate and fold inwards to create multiple layers. The place through which cells ingress is called the primitive streak. Cells that fail to ingress express a set of ectodermal precursor genes, while ingressing cells are stimulated to express a different set of genes, turning them into endoderm or mesoderm. Over the course of gastrulation, the primitive streak moves from anterior to posterior. Right below the streak, a mesodermal structure, called the notochord, develops, forming a signaling center.

Four stages of amniote gastrulation.
Figure 18.1. Amniote gastrulation. (A) At the start of gastrulation, precursor cells are arranged in a single layer, the epiblast. Gastrulation starts with ingression, where epiblast cells start to move forward and then to the middle, eventually ingressing below the eplblast, passing through the node and the primitive streak. (B) The node reaches to about 60% anterior, and then retracts. The node is a signaling center, turning on a set of genes that mark ingressing cells as mesodermal. The primitive streak and node retracts, leaving behind a cylinder of mesodermal cells along the midline (dotted red line) called the notochord. Other mesodermal cells migrate laterally. (C) Further regression of the primitive streak during gastrulation, leaving behind a growing notochord. (D) At the end of gastrulation, the embryo is transformed from from a single layered epiblast to a three-layered gastrula with ectoderm on top, mesoderm below, and endoderm at the bottom. At the same time, ectodermal cells close to the midline are specified as neuroectoderm, while the remaining ectoderm will develop into epidermal cells. Figure was adapted from Fig 22.1 by Casey Henley.

After gastrulation, the embryo is 3-layered, with a central primitive streak and an underlying notochord. Ectodermal cells closer to the primitive streak become neural, while cells on the periphery develop into epidermal precursors. The notochord, being a signaling center, secretes molecular signals that diffuse to the ectoderm above, and stimulate the formation of the neural tube.

Very early in development, an embryo looks like a flat disc with 3 different layers of cells.

  1. Endoderm: will eventually develop into the viscera (organs of the body)
  2. Mesoderm: will eventually develop into the bones and muscles
  3. Ectoderm: will eventually develop in the nervous system and the skin
Image of early embryo in cross section. Details in caption and text. 
Figure 18.2. Developmental layers of the embryo. Early in development, the embryo looks like a flat disc made up of three different layers (left image). The ectoderm layer is what will develop into the nervous system. A cross section of the embryo (right image) reveals the endoderm, mesoderm, and ectoderm layers. ‘Developmental layers of the embryo’ by Valerie Hedges is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

The Neural Tube

Next, part of the ectoderm will fold to form a nervous system precursor, a hollow neural tube, via the process called neurulation. Just prior to neurulation, the ectodermal layer has already been specified into centrally located neural precursors (magenta), flanking neural crest precursors (black), and epidermal precursors (yellow). Neural precursors will fold to form a neural tube (magenta). Neurulation  occurs within the first month following conception in humans. Neurulation starts at the anterior end, and progresses toward the posterior, though it leaves the neural tube open both at the anterior and all the way at the posterior. At the end of neurulation, the embryo has a hollow neural tube, separated from the remaining ectodermal cell layer above (yellow) which will form the epidermis. The flanking neural crest precursors come to lie between the neural tube and the epidermis, and will eventually migrate away from the midline. Below the neural tube lies mesodermal tissue, primarily in the form of a solid cylinder of cells called the notochord. Epidermis and notochord cells both secrete diffusible signals, which guide further differentiation of cells in the neural tube.

During neurulation, the middle of the neural plate folds first, followed by the anterior and posterior ends. The central nervous system will develop from the walls of the neural tube and the hollow lumen of the tube will become the cerebral ventricles and spinal canal within the central nervous system.

The neural tube is initially only one cell thick. These are the progenitor cells, which divide to create multiple layers, increasing in complexity from posterior (spinal cord) to the midbrain and at the anteriormost, the forebrain. Epidermal signals result in differentiation of cells in the dorsal part of the neural tube into sensory cells and interneurons, while the mesodermal signals from notochord result in ventral neural tube cells differentiating into motor neurons and interneurons.

FInally, neural crest cells (black, Fig 22.2) migrate away from the midline, differentiating into melanophores, Schwann cells, and neurons with cell bodies that are located outside the CNS – sensory neurons and cells of the enteric nervous system.

Neurulation: formation of the neural tube after gastrulation.
Figure 18.3. Neurulation. During the process of neurulation, the neural plate pinches together at the neural fold in the middle, and then closes at the anterior and posterior ends to form a neural tube. The structures of the central nervous system will form from the walls of the neural tube and the lumen of tube will become the ventricles of the brain and central canal of the spinal cord. Modified from ‘Neurulation’ by Valerie Hedges.

Neural Tube Defects

Early in pregnancy, there can be problems with the process of neurulation and the formation and closure of the neural tube. Collectively, these are referred to as neural tube defects that include defects that occur within the brain, spine, or spinal cord. One of the more common neural tube defects is spina bifida. In spina bifida, the neural tube fails to close completely, and as a result the backbone that typically protects the spinal cord also does not form appropriately. This event can occur anywhere along the spine, and will typically result in nerve damage at that particular site that will potentially lead to physical and / or intellectual disability ranging in severity with the degree of damage.

Anencephaly is a neural tube defect that is caused by the failure of the anterior portion of the neural tube to close. Anencephaly is a serious birth defect that typically prevents the development of the anterior portion of the brain and associated skull.

Unfortunately, many neural tube defects occur very early in pregnancy, such that many women do not yet know that they are pregnant. As a result, daily folic acid supplements or a diet that includes foods rich in folate is recommended to all women of reproductive age to help prevent neural tube defects in the event of a pregnancy.

Image of the neural tube defects spina bifida and anencephaly. Details in caption and text.
Figure 18.4. Neural Tube Defects. Spina bifida (left) occurs when the posterior neural tube fails to close. Anencephaly (right) occurs when the anterior neural tube fails to close, causing decreased development of the brain and skull. ‘Neural Tube Defects’ by Valerie Hedges is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Three Vesicle Stage of Development

Early in development, the anterior portion of the neural tube has three distinct vesicles, which will each develop into different structures. These vesicles, from most anterior to most posterior, are the prosencephalon (forebrain), the mesencephalon (midbrain), and the rhombencephalon (hindbrain).

Through development, the walls of these vesicles will differentiate into adult brain structures. Differentiation is the process by which structures become more complex and functionally specialized during development. The names of these early vesicles can be used to describe either the stages through development, or a grouping of structures that eventually form in adulthood. In the following chapters, we will learn more about some of these anatomical structures.

Image of the three vesicles of the anterior neural tube early in development. Details in caption and text.
Figure 18.5. Three vesicle stage of embryonic development. Early in development the anterior portion of the neural tube can be divided into three vesicles: the prosencephalon, the mesencephalon, and the rhombencephalon. ‘Three vesicle stage’ by Valerie Hedges is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Prosencephalon (Forebrain)

The prosencephalon, or the forebrain, is most anterior in the neural tube and eventually develops into the “higher order” brain regions, including the cerebral cortex. Most of the time, when you see an image of an intact brain from the side or the top, the structures that are visible to you are the forebrain structures. The prosencephalon is made up of the telencephalon and the diencephalon.

As the prosencephalon continues to develop, additional structures will form that are associated with the cerebral hemispheres. For instance, the optic vesicles that bud off the surface of the prosencephalon will differentiate into the retinas of the eyes—thus, the retina is made up of neural tissue. The olfactory bulbs will differentiate from the ventral surface of the cerebral hemispheres.

Note that as the walls of the tube develop into these structures, the lumen of the tube remains and will become the fluid-filled ventricles of the brain. The lateral ventricles will form from the tube within the cerebral hemispheres and the third ventricle will be found ventrally surrounded by the diencephalon.

Structures of the Telencephalon: Cerebral Cortex and the Basal Ganglia

The cerebral cortex makes up the outermost layer of the brain. The word “cortex” comes from the word meaning “bark”, the outer layer of a tree. The cerebral cortex is the most evolved structure of the human brain and is responsible for higher order thinking. Here, the brain processes behaviors such as attention, memory, and language.

The basal ganglia are made up of a series of brain structures (including the caudate and putamen, globus pallidus, substantia nigra, and subthalamic nucleus) that are used for such behaviors as motor and habit learning, emotional processing, and action selection.

 

Illustration of a coronal section of the brain showing the location of the basal ganglia and region names. Details in caption.
Figure 18.6. The basal ganglia are subcortical structures located at the base of the forebrain. They are comprised of the caudate and putamen, which both make up the striatum, as well as the globus pallidus, substantia nigra, and subthalamic nucleus. ‘Basal Ganglia’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Structures of the Diencephalon: Thalamus and Hypothalamus

The thalamus is often referred to as a “sensory relay station” in the brain, since almost every sensory modality (sight, taste, touch, and hearing) passes information through the thalamus before being directed to the appropriate area of the cortex.

The hypothalamus is also within the diencephalon. This structure serves as an autonomic control center to alter visceral function and a communication route to the body’s endocrine system through control of anterior pituitary hormones and production of posterior pituitary hormones. Neural signals originating in the hypothalamus have the capability to influence the chemistry and function of the entire body. The hypothalamus also has nuclei that function in emotional responses, and regulate body temperature, food intake, water balance, and sleep.

Illustration of a sagittal section of the brain showing the location of the hypothalamus and the pituitary.
Figure 18.7. The pituitary, shown in green in a mid-sagittal section, lies inferior to the hypothalamus, shown in blue. ‘Hypothalamus and Pituitary’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Mesencephalon

Moving more caudally, the mesencephalon (or the midbrain) differentiates into the tectum and the tegmentum.

Tectum

The tectum (which means “roof”) is the dorsal portion of the midbrain and it has two major structures: the superior colliculus and inferior colliculus. The superior colliculus is important in reflexive eye movements that allow you to quickly orient to something changing in your environment. The inferior colliculus relays auditory information to the thalamus for auditory function.

Tegmentum

The tegmentum (which means “floor”) is the ventral portion of the midbrain. There are many structures in the tegmentum and they can perform a wide variety of functions. For example, the periaqueductal gray allows us to respond to painful stimuli, the red nucleus and substantia nigra coordinate complex movements, and the ventral tegmental area is important for the processing of reward and motivation.

 

Illustration of the internal anatomy of the cerebrum and brainstem. Details in caption.
Figure 18.8. A midsagittal section of the brain. The midbrain (tectum and tegmentum) are located anterior to the pons. ‘Internal Brain Regions’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Rhombencephalon

The most posterior/caudal portion of the neural tube is the rhombencephalon (or hindbrain). Evolutionarily speaking, the rhombencephalon represents the oldest part of the central nervous system. These structures likely evolved some 570 million years ago.

Rostral Hindbrain

The more rostral portion of the hindbrain differentiates into two structures: the cerebellum and the pons. The cerebellum, or “little brain”, is best known as a structure that enables motor control functions, such as balance, coordination, posture, and learning physical actions. The cerebellum helps us recognize and predict sequences of events during motor learning. More recently, the cerebellum has also been recognized to play a role in non-motor functions like learning. The pons (which means “bridge”) is an important structure that relays impulses between the motor cortex and the cerebellum. It has a critical function to help us perform involuntary functions like breathing.

Caudal Hindbrain

The caudal portion of the hindbrain differentiates into the medulla. The medulla is found at the far posterior end of these three early developmental vesicles. The medulla contains many clumps of neurons that are responsible for functions that an organism carries out unconsciously. It contains a cardiovascular center that is especially important in maintaining and changing blood pressure and heart rate, and also has connections to the pons to help regulate breathing. The medulla contains areas that can detect toxins in the blood that come from dietary sources, triggering vomiting. Other behaviors like hiccupping, swallowing, coughing, and sneezing are also controlled by the medulla.

Moving beyond this anterior portion of the neural tube that contains the prosencephalon, mesencephalon, and rhombencephalon, the neural tube continues down the length of the embryo. The remainder of the neural tube will differentiate into the spinal cord, with the lumen of the tube becoming the central canal of the spinal cord. The spinal cord is important in relaying information to and from the body.

Image of structures of the rhombencephalon
Figure 18.9. Structures of the rhombencephalon. The rostral portion of the rhombencephalon develops into the cerebellum and pons. The caudal portion of the of the rhombencephalon develops into the medulla. The spinal cord is connected to the posterior end of the medulla and continues down the length of the spine. ‘Structures of the rhombencephalon’ by Valerie Hedges is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Key Takeaways

  • The ectoderm layer of the embryo develops into the nervous system
  • Neurulation is the process that forms the neural tube and failure for portions of the neural tube to close can cause neural tube defects
  • The prosencephalon, mesencephalon, and rhombencephalon are the three vesicles at the anterior end of the neural tube. They will develop into structures in the adult brain.

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Attributions

This chapter is adapted from “Brain Structure Differentiation” in Introduction to Neuroscience by Valerie Hedges which is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

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Introduction to Neurobiology Copyright © 2024 by Avinash Singh is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, except where otherwise noted.

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