Abstract
Neurotrophin-3 (NT-3) and its receptor TrkC are known to be important for neuronal survival. More recently, NT-3 has been implicated as playing a role in oligodendrocyte (OL) proliferation and survival in vitro. Examination of NT-3 and TrkC knockout mice revealed a reduction in NT-3-dependent neurons. To date, no study has examined alterations in glial cell populations in these knockout mice. In this report, we demonstrate a decline in OL progenitor cell numbers within the CNS of NT-3 and TrkC knockout mice. We also observed that immature and mature OL-specific markers were attenuated in the NT-3 and TrkC knockout animals. Deficiencies in other CNS glial cells, including astrocytes and ameboid microglia, were also observed. The subventricular zone (SVZ), a highly proliferative region for progenitor glial cells, was reduced in size. Furthermore, a nuclear-specific stain revealed a decline in the numbers of pyknotic nuclei in and around the SVZ of the knockout mice. These data will support an in vivo NT-3-dependent mechanism for the normal development of CNS glial cells.
Original language | English (US) |
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Pages (from-to) | 153-165 |
Number of pages | 13 |
Journal | GLIA |
Volume | 26 |
Issue number | 2 |
DOIs | |
State | Published - 1999 |
Keywords
- Astrocytes
- CNS
- Glia
- Microglia
- Neurotrophin-3
- Oligodendrocytes
- TrkC
ASJC Scopus subject areas
- Neurology
- Cellular and Molecular Neuroscience