| Popis: |
In the spinal cord, most oligodendrocytes, the myelinating cell type of the CNS, and motor neurons arise from common, ventral, olig2-expressing precursors called pMN cells. In the hindbrain, the degree to which motor neurons and oligodendrocytes share common origins and, consequently, are specified by similar molecular mechanisms is not clear. This ambiguity results, at least in part, from the fact that both oligodendrocyte progenitor cells (OPCs) and some motor neurons migrate, obscuring whether these cells have common or distinct origins. Therefore, we used zebrafish as a model system to investigate hindbrain motor neuron and oligodendrocyte development. We found, using cell specific markers, transgenic reporter lines and time-lapse microscopy, that a subset of OPCs and abducens motor neurons, which control eye movement, arise from common olig2-expressing precursors in rhombomeres (r) 5 and 6. To investigate the role of olig2, we reduced its function using translation-blocking morpholino oligonucleotides. This produced deficits of OPCs and abducens motor neurons, but not other motor neuron populations. However, we also found that facial motor neurons failed to complete their migration from r4 into r6 and r7. This raises the possibility that the olig2+ precursors provide a positional cue necessary for facial motor neuron migration. A better understanding of proper OPC and neuronal specification and migration in the hindbrain will bring increased insight to motor neuron disorders such as Mobius Syndrome and Duane Syndrome, which affect the facial and abducens motor neurons, respectively, as well as demyelinating disorders, such as Multiple Sclerosis. |
