Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

The Transcription Factors COUP-TFI and COUP-TFII have Distinct Roles in Arealisation and GABAergic Interneuron Specification in the Early Human Fetal Telencephalon

Lookup NU author(s): Ayman Alzu'bi, Emerita Professor Susan Lindsay, Lauren Harkin, Dr Steven LisgoORCiD, Dr Gavin ClowryORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

In human telencephalon at 8–12 postconceptional weeks, ribonucleic acid quantitative sequencing andimmunohistochemistry revealed cortical chicken ovalbumin upstream promotor-transcription factor 1 (COUP-TFI)expression in a high ventro-posterior to low anterior gradient except for raised immunoreactivity in the anterior ventralpallium. Unlike in mouse, COUP-TFI and SP8 were extensively co-expressed in dorsal sensory neocortex and dorsalhippocampus whereas COUPTFI/COUPTFII co-expression defined ventral temporal cortex and ventral hippocampus. In theganglionic eminences (GEs) COUP-TFI immunoreactivity demarcated the proliferative zones of caudal GE (CGE), dorsalmedial GE (MGE), MGE/lateral GE (LGE) boundary, and ventral LGE whereas COUP-TFII was limited to ventral CGE and theMGE/LGE boundary. Co-labeling with gamma amino butyric acidergic interneuron markers revealed that COUP-TFI wasexpressed in subpopulations of either MGE-derived (SOX6+) or CGE-derived (calretinin+/SP8+) interneurons. COUP-TFII wasmainly confined to CGE-derived interneurons. Twice as many GAD67+ cortical cells co-labeled for COUP-TFI than for COUPTFII.A fifth of COUP-TFI cells also co-expressed COUP-TFII, and cells expressing either transcription factor followedposterior or anterio-lateral pathways into the cortex, therefore, a segregation of migration pathways according to COUP-TFexpression as proposed in mouse was not observed. In cultures differentiated from isolated human cortical progenitors,many cells expressed either COUP-TF and 30% also co-expressed GABA, however no cells expressed NKX2.1. This suggestsinterneurons could be generated intracortically from progenitors expressing either COUP-TF.


Publication metadata

Author(s): Alzu'bi A, Lindsay SJ, Harkin LF, McIntyre J, Lisgo SN, Clowry GJ

Publication type: Article

Publication status: Published

Journal: Cerebral Cortex

Year: 2017

Volume: 27

Issue: 10

Pages: 4971-4987

Print publication date: 01/10/2017

Online publication date: 09/08/2017

Acceptance date: 03/07/2017

Date deposited: 07/09/2017

ISSN (print): 1047-3211

ISSN (electronic): 1460-2199

Publisher: Oxford University Press

URL: https://doi.org/10.1093/cercor/bhx185

DOI: 10.1093/cercor/bhx185


Altmetrics

Altmetrics provided by Altmetric


Funding

Funder referenceFunder name
099175/Z/12/ZWellcome Trust
MC/PC/13047

Share