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Related Concept Videos

Neurulation01:30

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the anterior...
Neurons: The Axon01:21

Neurons: The Axon

Axons are long, cytoplasmic processes of nerve cells capable of propagating electrical impulses known as action potentials. The cytoplasm or axoplasm of an axon contains neurofibrils, neurotubules, small vesicles, lysosomes, mitochondria, and various enzymes, all encased within the axolemma, the plasma membrane of the axon.
The axon attaches to the cell body at a cone-shaped elevation called the axon hillock. The initial part of the axon, closest to the hillock, is known as the initial segment.
Nervous Tissue: Myelin01:25

Nervous Tissue: Myelin

The myelin sheath is a multilayered lipid and protein covering that insulates the axon of a neuron, enhancing the speed of nerve impulse conduction. Axons without this sheath are referred to as unmyelinated. Two types of neuroglia, Schwann cells in the peripheral nervous system (PNS) and oligodendrocytes in the central nervous system (CNS) are responsible for producing myelin sheaths.
Schwann cells begin to form myelin sheaths around axons during fetal development. They wrap around a small...
Neurogenesis and Regeneration of Nervous Tissue01:15

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In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
Spinal Cord: Information Processing01:10

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The spinal cord is an integral hub for motor and sensory information that enables the brain to communicate with the peripheral nervous system (PNS). This communication consists of relaying sensory data and transmission of motor commands.
Sensory Information Processing
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Functions of the Nervous System

The nervous system is responsible for coordinating and regulating the body's functions. It functions through three main processes: sensory, integrative, and motor processes. Sensory function involves the detection and transmission of information about internal and external stimuli from sensory receptors to the CNS. The CNS processes this information through an integrative function, where it interprets and makes decisions based on the incoming sensory information. Finally, the motor function...

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Related Experiment Video

Updated: Jul 11, 2026

Three-Dimensional Motor Nerve Organoid Generation
09:57

Three-Dimensional Motor Nerve Organoid Generation

Published on: September 24, 2020

Initial motor axon outgrowth from the developing central nervous system.

J P Fraher1, P Dockery, O O'Donoghue

  • 1Department of Anatomy, BioSciences Institute, University College Cork, Cork, Ireland.

Journal of Anatomy
|September 14, 2007
PubMed
Summary
This summary is machine-generated.

Motor rootlet axon bundles emerge from the neural tube, facilitated by radial glial end feet. Unlike sensory rootlets, motor exit points lack boundary cap cells during development.

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Area of Science:

  • Developmental Neuroscience
  • Neurobiology
  • Embryology

Background:

  • The formation and guidance of motor and sensory rootlets are critical for establishing nervous system circuitry.
  • Understanding the cellular and molecular mechanisms governing rootlet emergence is essential for comprehending neural development.

Purpose of the Study:

  • To investigate the cellular interactions and morphological features at the emergence points of motor and sensory rootlets from the neural tube.
  • To differentiate the developmental pathways of motor versus sensory rootlet exit points.

Main Methods:

  • Comparative histological analysis of rat and chick embryos during neural tube development.
  • Microscopic examination of radial glial end feet, basal lamina, and associated cell clusters at motor and sensory rootlet exit sites.

Main Results:

  • Earliest motor rootlet axon bundles emerge through presumptive glia limitans, facilitated by loosely arranged radial glial end feet.
  • Motor rootlets acquire a basal lamina sleeve from the neural tube surface and later associate with peripheral cell clusters.
  • A tight collar of glial end feet forms around motor axon bundles post-emergence, contrasting sharply with sensory rootlets.
  • Sensory rootlets exhibit prefigured entry zones by boundary cap cells, which are absent at motor exit points.

Conclusions:

  • Motor rootlet emergence is a distinct process from sensory rootlet development, characterized by glial end feet facilitation and the absence of boundary cap cells.
  • The findings highlight species-specific (rat, chick) cellular arrangements during early motor axon pathfinding from the neural tube.