Neural tube in the context of "Neurulation"

The brain is an organ that serves as the center of the nervous system in all vertebrate and most invertebrate animals. It consists of nervous tissue and is typically located in the head (cephalization), usually near organs for special senses such as vision, hearing, and olfaction. Being the most specialized organ, it is responsible for receiving information from the sensory nervous system, processing that information (thought, cognition, and intelligence) and the coordination of motor control (muscle activity and endocrine system).

While invertebrate brains arise from paired segmental ganglia (each of which is only responsible for the respective body segment) of the ventral nerve cord, vertebrate brains develop axially from the midline dorsal nerve cord as a vesicular enlargement at the rostral end of the neural tube, with centralized control over all body segments. All vertebrate brains can be embryonically divided into three parts: the forebrain (prosencephalon, subdivided into telencephalon and diencephalon), midbrain (mesencephalon) and hindbrain (rhombencephalon, subdivided into metencephalon and myelencephalon). The spinal cord, which directly interacts with somatic functions below the head, can be considered a caudal extension of the myelencephalon enclosed inside the vertebral column. Together, the brain and spinal cord constitute the central nervous system in all vertebrates.

A chordate (/ˈkɔːrdeɪt/ KOR-dayt) is a bilaterian animal belonging to the phylum Chordata (/kɔːrˈdeɪtə/ kor-DAY-tə). All chordates possess, at some point during their larval or adult stages, five distinctive physical characteristics (synapomorphies) that distinguish them from other taxa. These five synapomorphies are a notochord, a hollow dorsal nerve cord, an endostyle or thyroid, pharyngeal slits, and a post-anal tail.

In addition to the morphological characteristics used to define chordates, analysis of genome sequences has identified two conserved signature indels (CSIs) in their proteins: cyclophilin-like protein and inner mitochondrial membrane protease ATP23, which are exclusively shared by all vertebrates, tunicates and cephalochordates. These CSIs provide molecular means to reliably distinguish chordates from all other animals.

Brain vesicles are the bulge-like enlargements of the early development of the neural tube in vertebrates, which eventually give rise to the brain.

Vesicle formation begins shortly after the rostral closure of the neural tube, at about embryonic day 9.0 in mice, or the fourth and fifth gestational week in humans. In zebrafish and chicken embryos, brain vesicles form by about 24 hours and 48 hours post-conception, respectively.

In the human brain, the diencephalon (or interbrain) is a division of the forebrain (embryonic prosencephalon). It is situated between the telencephalon and the midbrain (embryonic mesencephalon). The diencephalon has also been known as the tweenbrain in older literature. It consists of structures that are on either side of the third ventricle, including the thalamus, the hypothalamus, the epithalamus and the subthalamus.

The diencephalon is one of the main vesicles of the brain formed during embryonic development. During the third week of development a neural tube is created from the ectoderm, one of the three primary germ layers, and forms three main vesicles: the prosencephalon, the mesencephalon and the rhombencephalon. The prosencephalon gradually divides into the telencephalon (the cerebrum) and the diencephalon.

The central canal (also known as spinal foramen or ependymal canal) is the cerebrospinal fluid-filled space that runs through the spinal cord. The central canal lies below and is connected to the ventricular system of the brain, from which it receives cerebrospinal fluid, and shares the same ependymal lining. The central canal helps to transport nutrients to the spinal cord as well as protect it by cushioning the impact of a force when the spine is affected.

The central canal represents the adult remainder of the central cavity of the neural tube. It generally occludes (closes off) with age.

Neuroepithelial cells, or neuroectodermal cells, form the wall of the closed neural tube in early embryonic development. The neuroepithelial cells span the thickness of the tube's wall, connecting with the pial surface and with the ventricular or lumenal surface. They are joined at the lumen of the tube by junctional complexes, where they form a pseudostratified layer of epithelium called neuroepithelium.

Neuroepithelial cells are the stem cells of the central nervous system, known as neural stem cells, and generate the intermediate progenitor cells known as radial glial cells, that differentiate into neurons and glia in the process of neurogenesis.

The neuraxis, also known as the neuroaxis is the axis of the central nervous system. It extends from the brain to the spinal cord and denotes the direction in which the central nervous system lies in both development and in mature organisms. Early on in embryological development, the neuraxis begins as a distinctly straight axis, but quickly develops bends by various flexures, most notably the cephalic flexure, which contributes most to the complex mature structure of the spinal cord and brain.

Embryonic development can help in understanding how complex structures form around the neuraxis The embryonic nervous system in vertebrates is highly conserved, meaning its structure and function have stayed the same across species, and generally appear the same. During development, the formation of the neural tube-and later the brain and spinal cord- define the layout of the neuraxis. This establishes the anterior-posterior dimension of the nervous system. The anterior-posterior dimension of the neuraxis overlays the superior-inferior dimension of the body. Depending on the formation of more differentiated structures, this axis may lose its rigid nature, adopting the curvature introduced by encephalic structures. For example, there is a major curve between the brain stem and forebrain, which is called the cephalic flexure. Because of this, the neuraxis starts in an inferior position—the end of the spinal cord—and ends in an anterior position, the front of the cerebrum. This can be illustrated when looking at a four-legged animal standing up on two legs. Without this flexure in the brain stem and at the top of the neck, a bipedal animal would be unable to look directly in front of them.