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Lesion‐induced generation of interneuron cell types in specific dorsoventral domains in the spinal cord of adult zebrafish
Author(s) -
Kuscha Veronika,
Frazer Sarah L.,
Dias Tatyana B.,
Hibi Masahiko,
Becker Thomas,
Becker Catherina G.
Publication year - 2012
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.23115
Subject(s) - biology , interneuron , spinal cord , zebrafish , olig2 , neuroscience , progenitor cell , anatomy , population , lesion , green fluorescent protein , central nervous system , inhibitory postsynaptic potential , microbiology and biotechnology , pathology , stem cell , medicine , oligodendrocyte , biochemistry , myelin , environmental health , gene
In contrast to mammals, adult zebrafish regenerate neurons in the lesioned spinal cord. For example, motor neurons are generated from an olig2‐expressing population of pMN‐like ependymoradial glial cells in a ventrolateral position at the central canal. However, the extent of neuronal regeneration is unclear. Here we show, using a transgenic fish in which V2 interneurons are labeled by green fluorescent protein (GFP) under the control of the vsx1 promoter, that after a complete spinal cord transection, large numbers of V2 interneurons are generated in the vicinity of the lesion site. Tg(vsx1:GFP) + cells are not present in the unlesioned spinal cord and label with the proliferation marker bromodeoxyuridine (BrdU) after a lesion. Some mediolaterally elongated Tg(vsx1:GFP) + cells contact the central canal in a medial position. These cells likely arise from a p2‐like domain of ependymoradial glial progenitor cells, indicated by coexpression of Pax6 and Nkx6.1, but not DsRed driven by the olig2 promoter in these cells. We also present evidence that Pax2 + interneurons are newly generated after a spinal lesion, whereas the generation rate for a dorsal population of parvalbuminergic interneurons is comparatively low. Our results identify the regenerative potential of different interneuron types for the first time and support a model in which different progenitor cell domains in distinct dorsoventral positions around the central canal are activated by a lesion to give rise to diverse neuronal cell types in the adult zebrafish spinal cord. J. Comp. Neurol. 520:3604–3616, 2012. © 2012 Wiley Periodicals, Inc.