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Transcriptional profile of migrating GABAergic progentitors in the E14 mouse brain following maternal exposure to cypermethrin and restraint stress

ABSTRACT: Transcriptional profile of migrating GABAergic progentitors in the E14 mouse brain following maternal exposure to cypermethrin and restraint stress

PROVIDER: PRJNA603850 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR10987767_1.fastq.gz	Fastqsanger.gz
	SRR10987767_2.fastq.gz	Fastqsanger.gz
	SRR10987768_1.fastq.gz	Fastqsanger.gz
	SRR10987768_2.fastq.gz	Fastqsanger.gz
	SRR10987769_1.fastq.gz	Fastqsanger.gz

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Transcriptional profile of migrating GABAergic progentitors in the E14 mouse brain following maternal exposure to cypermethrin and restraint stress

Project description:The goal of this experiment was to assess transcriptional changes in isolated GABAergic progenitors to determine the mechanism by which prenatal exposure to cypermethrin and maternal stress alter their migration

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Project description:Transplantation of GABAergic interneurons (INs) can sustain long-standing benefits in animal models of epilepsy and other neurological disorders. In a therapeutic perspective, a renewable source of functional GABAergic INs is needed. Here, we identified five factors (Foxg1, Sox2, Ascl1, Dlx5 and Lhx6) able to convert fibroblasts directly into induced GABAergic INs (iGABA-INs), displaying the molecular signature of telencephalic INs. The selected factors recapitulate in fibroblasts the activation of transcriptional networks required for the specification of GABAergic fate during telencephalon development. iGABA-INs exhibited progressively maturing firing patterns comparable to those of cortical INs, had synaptic currents and released GABA. Importantly, upon grafting in the hippocampus, iGABA-INs survived, matured and their optogenetic stimulation triggered GABAergic transmission and inhibited the activity of connected granule cells. The five factors also converted human cells into functional GABAergic neurons. These properties define iGABA-INs as a promising tool for disease modeling and cell-based therapeutic approaches. Comparison of iGABA-INs transcriptional profile with those of starting fibroblasts and GAD67-GFP+ cortical interneurons.

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