In:
eLife, eLife Sciences Publications, Ltd, Vol. 7 ( 2018-08-09)
Abstract:
The cerebellum, or 'little brain', handles movement, thought and social interaction. Unlike the rest of the brain, which primarily develops in the womb, most of its cells appear within the first year of our lives (or first few weeks in mice). This makes it vulnerable to injury around the time of birth. We used to think that the brain could not replace damaged neurons, but when specific precursor cells in the cerebellum in the brains of newborn mice are removed, they are able to renew themselves. This is because specialized stem cells start to divide and produce the missing cells of the cerebellum. Another type of cells in the cerebellum, called Purkinje neurons, are already produced in the embryo. They direct the development of several other cell types in the cerebellum after birth. They are also a crucial component of the circuits within the cerebellum, and losing them can cause loss of muscle coordination. Purkinje cells do not normally divide once an animal is born, but scientists want to know if they might be able to regrow after injury at birth. Bayin et al. killed Purkinje cells in newborn mice with a toxin and used fluorescent markers to track the dying cells. Then, the remaining cells in the surrounding area were studied. This revealed that even when half of the Purkinje cells died a day after birth, the mice behaved normally. The cells regrew, and the cerebellum developed as it should. This happened because the loss of the Purkinje cells activated a population of immature Purkinje cells (iPCs). These cells would normally mature into adult Purkinje cells, but in their immature state they can still divide and make copies of themselves to replace lost neurons after injury. As the mice grew older, the number of iPCs started to drop as the immature cells developed into adult Purkinje cells. When the iPCs ran out, any cells available to divide were gone and the mice could no longer replace any damaged Purkinje cells – the repair window had closed. This work raises the possibility that other types of immature cells in the brain could be set aside to help repair damage during early development. A better understanding of these cells could reveal clues about conditions such as autism, which have been linked to damages or faults in the cerebellum. It may also help to gain new insights into how to regenerate the adult brain after injury.
Type of Medium:
Online Resource
ISSN:
2050-084X
DOI:
10.7554/eLife.39879.001
DOI:
10.7554/eLife.39879.002
DOI:
10.7554/eLife.39879.003
DOI:
10.7554/eLife.39879.007
DOI:
10.7554/eLife.39879.008
DOI:
10.7554/eLife.39879.004
DOI:
10.7554/eLife.39879.005
DOI:
10.7554/eLife.39879.006
DOI:
10.7554/eLife.39879.009
DOI:
10.7554/eLife.39879.010
DOI:
10.7554/eLife.39879.011
DOI:
10.7554/eLife.39879.012
DOI:
10.7554/eLife.39879.013
DOI:
10.7554/eLife.39879.014
DOI:
10.7554/eLife.39879.015
DOI:
10.7554/eLife.39879.016
DOI:
10.7554/eLife.39879.017
DOI:
10.7554/eLife.39879.018
DOI:
10.7554/eLife.39879.019
DOI:
10.7554/eLife.39879.020
DOI:
10.7554/eLife.39879.021
DOI:
10.7554/eLife.39879.022
DOI:
10.7554/eLife.39879.023
DOI:
10.7554/eLife.39879.024
DOI:
10.7554/eLife.39879.025
DOI:
10.7554/eLife.39879.026
DOI:
10.7554/eLife.39879.027
DOI:
10.7554/eLife.39879.028
DOI:
10.7554/eLife.39879.029
DOI:
10.7554/eLife.39879.030
DOI:
10.7554/eLife.39879.033
DOI:
10.7554/eLife.39879.034
DOI:
10.7554/eLife.39879.032
Language:
English
Publisher:
eLife Sciences Publications, Ltd
Publication Date:
2018
detail.hit.zdb_id:
2687154-3