Spinal motor neurons are regenerated after mechanical lesion and genetic ablation in larval zebrafish

Ohnmacht J, Yang Y, Maurer GW, Barreiro-Iglesias A, Tsarouchas TM, Wehner D, Sieger D, Becker CG, Becker T (2016)


Publication Type: Journal article

Publication year: 2016

Journal

Book Volume: 143

Pages Range: 1464-1474

Journal Issue: 9

DOI: 10.1242/dev.129155

Abstract

In adult zebrafish, relatively quiescent progenitor cells show lesioninduced generation of motor neurons. Developmental motor neuron generation from the spinal motor neuron progenitor domain (pMN) sharply declines at 48 hours post-fertilisation (hpf). After that, mostly oligodendrocytes are generated from the same domain. We demonstrate here that within 48 h of a spinal lesion or specific genetic ablation of motor neurons at 72 hpf, the pMN domain reverts to motor neuron generation at the expense of oligodendrogenesis. By contrast, generation of dorsal Pax2-positive interneurons was not altered. Larval motor neuron regeneration can be boosted by dopaminergic drugs, similar to adult regeneration. We use larval lesions to show that pharmacological suppression of the cellular response of the innate immune system inhibits motor neuron regeneration. Hence, we have established a rapid larval regeneration paradigm. Either mechanical lesions or motor neuron ablation is sufficient to reveal a high degree of developmental flexibility of pMN progenitor cells. In addition, we show an important influence of the immune system on motor neuron regeneration from these progenitor cells.

Involved external institutions

How to cite

APA:

Ohnmacht, J., Yang, Y., Maurer, G.W., Barreiro-Iglesias, A., Tsarouchas, T.M., Wehner, D.,... Becker, T. (2016). Spinal motor neurons are regenerated after mechanical lesion and genetic ablation in larval zebrafish. Development, 143(9), 1464-1474. https://doi.org/10.1242/dev.129155

MLA:

Ohnmacht, Jochen, et al. "Spinal motor neurons are regenerated after mechanical lesion and genetic ablation in larval zebrafish." Development 143.9 (2016): 1464-1474.

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