Wong, Chee Ern David and Hua, Khang and Monis, Simon and Saxena, Vishal and Norazit, Anwar and Mohd Noor, Suzita and Ekker, Marc (2021) gdnf affects early diencephalic dopaminergic neuron development through regulation of differentiation-associated transcription factors in zebrafish. Journal of Neurochemistry, 156 (4). pp. 481-498. ISSN 0022-3042, DOI https://doi.org/10.1111/jnc.15108.
Full text not available from this repository.Abstract
Glial cell line-derived neurotrophic factor (GDNF) has been reported to enhance dopaminergic neuron survival and differentiation in vitro and in vivo, although those results are still being debated. Glial cell line-derived neurotrophic factor (gdnf) is highly conserved in zebrafish and plays a role in enteric nervous system function. However, little is known about gdnf function in the teleost brain. Here, we employed clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 to impede gdnf function in the maintenance of dopaminergic neuron development. Genotyping of gdnf crispants revealed successful deletions of the coding region with various mutant band sizes and down-regulation of gdnf transcripts at 1, 3 and 7 day(s) post fertilization. Notably, similar to 20% reduction in ventral diencephalic dopaminergic neuron numbers in clusters 8 and 13 was observed in the gdnf-deficient crispants. In addition,gdnf depletion caused a modest reduction in dopaminergic neurogenesis as determined by 5-ethynyl-2'-deoxyuridine pulse chase assay. These deleterious effects could be partly attributed to deregulation of dopaminergic neuron fate specification-related transcription factors (otp, lmx1b, shha, and ngn1) in both crispants and established homozygous mutants with whole mount in-situ hybridization(WISH) on gdnf mutants showing reduced otpb and lmx1b.1 expression in the ventral diencephalon. Interestingly, locomotor function of crispants was only impacted at 7 dpf, but not earlier. Lastly, as expected, gdnf deficiency heightened crispants vulnerability to 1-methyl-4-phenylpyridinium toxic insult. Our results suggest conservation of teleost gdnf brain function with mammals and revealed the interactions between gdnf and transcription factors in dopaminergic neuron differentiation.
| Item Type: | Article |
|---|---|
| Funders: | Malaysian Ministry of Higher Education Fundamental Research Grant Scheme [FP027-2014A], Natural Sciences and Engineering Research Council of Canada (NSERC) CGIAR [121795], Universiti Malaya [PG246-2015B], Special Research Assistance grant [BKS064-2017], Research University Grant (Faculty of Medicine RU) [GPF014C-2018], Malaysian Ministry of Higher Education "MyPhD programme", Malaysian Society of Neurosciences Education Grant [02246] |
| Uncontrolled Keywords: | Crispants; Differentiation; Dopaminergic neurons; gdnf; Knock-out; Neurogenesis; Transcription factors; Ventral diencephalon |
| Subjects: | Q Science > QD Chemistry Q Science > QH Natural history > QH301 Biology R Medicine > RC Internal medicine |
| Divisions: | Faculty of Medicine |
| Depositing User: | Ms Zaharah Ramly |
| Date Deposited: | 18 Aug 2022 01:07 |
| Last Modified: | 18 Aug 2022 01:07 |
| URI: | http://eprints.um.edu.my/id/eprint/28765 |
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