Neuroblast

A neuroblast or primitive nerve cell[1] is a postmitotic cell that does not divide further,[2] and which will develop into a neuron after a migration phase.[3] Neuroblasts differentiate from radial glial cells and are committed to becoming neurons.[4] Neural stem cells, which only divide symmetrically to produce more neural stem cells, transition gradually into radial glial cells.[5] Radial glial cells, also called radial glial progenitor cells, divide asymmetrically to produce a neuroblast and another radial glial cell that will re-enter the cell cycle.[5][3]

This mitosis occurs in the germinal neuroepithelium (or germinal zone), when a radial glial cell divides to produce the neuroblast. The neuroblast detaches from the epithelium and migrates while the radial glial progenitor cell produced stays in the lumenal epithelium. The migrating cell will not divide further and this is called the neuron's birthday. Cells with the earliest birthdays will only migrate a short distance. Those cells with later birthdays will migrate further to the more outer regions of the cerebral cortex. The positions that the migrated cells occupy will determine their neuronal differentiation.[6]

Formation

Neuroblasts are formed by the asymmetric division of radial glial cells. They start to migrate as soon as they are born. Neurogenesis can only take place when neural stem cells have transitioned into radial glial cells.[5]

Differentiation

Neuroblasts are mainly present as precursors of neurons during embryonic development; however, they also constitute one of the cell types involved in adult neurogenesis. Adult neurogenesis is characterized by neural stem cell differentiation and integration in the mature adult mammalian brain. This process occurs in the dentate gyrus of the hippocampus and in the subventricular zones of the adult mammalian brain. Neuroblasts are formed when a neural stem cell, which can differentiate into any type of mature neural cell (i.e. neurons, oligodendrocytes, astrocytes, etc.), divides and becomes a transit amplifying cell. Transit amplifying cells are slightly more differentiated than neural stem cells and can divide asymmetrically to produce postmitotic neuroblasts and glioblasts, as well as other transit amplifying cells. A neuroblast, a daughter cell of a transit amplifying cell, is initially a neural stem cell that has reached the "point of no return." A neuroblast has differentiated such that it will mature into a neuron and not any other neural cell type.[7] Neuroblasts are being studied extensively as they have the potential to be used therapeutically to combat cell loss due to injury or disease in the brain, although their potential effectiveness is debated.

Migration

In the embryo neuroblasts form the middle mantle layer of the neural tube wall which goes on to form the grey matter of the spinal cord. The outer layer to the mantle layer is the marginal layer and this contains the myelinated axons from the neuroblasts forming the white matter of the spinal cord.[1] The inner layer is the ependymal layer that will form the lining of the ventricles and central canal of the spinal cord.[8]

In humans, neuroblasts produced by stem cells in the adult subventricular zone migrate into damaged areas after brain injuries. However, they are restricted to the subtype of small interneuron-like cells, and it is unlikely that they contribute to functional recovery of striatal circuits.[9]

Clinical significance

There are several disorders known as neuronal migration disorders that can cause serious problems. These arise from a disruption in the pattern of migration of the neuroblasts on their way to their target destinations. The disorders include, lissencephaly, microlissencephaly, pachygyria, and several types of gray matter heterotopia.

Neuroblast development in Drosophila

The study of the development of neuroblasts has been carried out largely on the fruit fly model organism Drosophila melanogaster.[10] Up until 2017 eight Nobel Prizes have been awarded for research on this organism.

In the neuroectoderm, small clusters of equivalent cells acquire the potential to become neuroblasts, through the expression of proneural genes. From there, one particular cell from each cluster is selected to become a neuroblast, through the action of the Notch signaling pathway. Once the future neuroblast cells are selected, they delaminate, then carry on dividing for a pre-programmed number of divisions.

Neuroblasts divide asymmetrically at every stage, creating one cell that continues being a neuroblast, and one cell that becomes the ganglion mother cell (GMC), which goes on to divide into 4 differentiated cells (neurons or glia). The switch from pluripotent neuroblast to differentiated cell fate is facilitated by the proteins Prospero, Numb, and Miranda. Prospero is a transcription factor that triggers differentiation. It is expressed in neuroblasts, but is kept out of the nucleus by Miranda, which tethers it to the cell basal cortex. This also results in asymmetric division, where Prospero localizes in only one out of the two daughter cells. After division, Prospero enters the nucleus, and the cell it is present in becomes the GMC.

Each neuroblast goes on to create a specific sequence of cells with particular identities. This is partly based on the position of the neuroblast along the Anterior/Posterior and Dorsal/Ventral axes, and partly on a temporal sequence of transcription factors that are expressed in a specific order as neuroblasts undergo sequential divisions.

See also

• Neuroblastoma
• Posterior column
• List of human cell types derived from the germ layers

References

1. Sadler, T. (2010). Langman's medical embryology (11th ed.). Philadelphia: Lippincott William & Wilkins. pp. 296–297. ISBN 978-07817-9069-7.
2. Williams, S. Mark (2001). "The Initial Formation of the Nervous System: Gastrulation and Neurulation". Neuroscience. 2nd edition. Retrieved 5 January 2019.
3. Purves, Dale (2012). Neuroscience (5th ed.). Sinauer Associates. p. 490. ISBN 9780878936953.
4. "wberesford.hsc.wvu.edu". Retrieved 2010-04-08.
5. Johnson, CA; Wright, CE; Ghashghaei, HT (December 2017). "Regulation of cytokinesis during corticogenesis: focus on the midbody". FEBS Letters. 591 (24): 4009–4026. doi:10.1002/1873-3468.12676. PMID 28493553.
6. Gilbert, Scott (2006). Developmental biology (8th ed.). Sinauer Associates Publishers. pp. 386–387. ISBN 9780878932504.
7. Purves, D; et al. (2007). Neuroscience (4th ed.). New York: W. H. Freeman. ISBN 978-0-87893-697-7.
8. Tortora, G; Derrickson, B (2011). Principles of anatomy & physiology (13th. ed.). Wiley. p. 571. ISBN 9780470646083.
9. Liu, F; You, Y; Li, X; Ma, T; Nie, Y; Wei, B; Li, T; Lin, H; Yang, Z (April 2009). "Brain Injury Does Not Alter the Intrinsic Differentiation Potential of Adult Neuroblasts". The Journal of Neuroscience. 29 (16): 5075–5087. doi:10.1523/JNEUROSCI.0201-09.2009. PMID 19386903.
10. Gallaud, E; Pham, T; Cabernard, C (2017). "Drosophila melanogaster Neuroblasts: A Model for Asymmetric Stem Cell Divisions". Results and problems in cell differentiation. 61: 183–210. doi:10.1007/978-3-319-53150-2_8. PMID 28409305.