Fate plasticity of interneuron specification

Neuronal subtype generation in the mammalian central nervous system is governed by competing genetic programs. The medial ganglionic eminence (MGE) produces two major cortical interneuron (IN) populations, somatostatin (Sst) and parvalbumin (Pvalb), which develop on different timelines. The extent to which external signals influence these identities remains unclear. Pvalb-positive INs are crucial for cortical circuit regulation but challenging to model <i>in vitro</i>. We grafted mouse MGE progenitors into diverse 2D and 3D co-culture systems, including mouse and human cortical, MGE, and thalamic models. Strikingly, only 3D human corticogenesis models promoted efficient, non-autonomous Pvalb differentiation, characterized by upregulation of Pvalb maturation markers, downregulation of Sst-specific markers, and the formation of perineuronal nets. Additionally, lineage-traced postmitotic Sst-positive INs upregulated Pvalb when grafted onto human cortical models. These findings reveal unexpected fate plasticity in MGE-derived INs, suggesting that their identities can be dynamically shaped by the environment.

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Publication Details

Journal
iScience
Published
2025-03-27
DOI
https://doi.org/10.1016/j.isci.2025.112295
Citations
7
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
6.67

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article

Fate plasticity of interneuron specification

Madeline G. Andrews, Jesus Gonzalez-Ferrer, Mircea Teodorescu, Arnold R. Kriegstein et al.
7 citations
iScience
Genetics, Aging, and Longevity in Model Organisms
6.67
article

Fate plasticity of interneuron specification

Madeline G. Andrews, Jesus Gonzalez-Ferrer, Mircea Teodorescu, Arnold R. Kriegstein, Mercedes F. Paredes, Ash Robbins, Arturo Álvarez-Buylla, Mohammed A. Mostajo-Radji, Walter Mancia, Matthew T. Schmitz, Yonatan Perez, Alex A. Pollen, Tanzila Mukhtar, H. Schweiger, Julian Lehrer, Arnar Breevoort, Darío Tejera, Frederika N. Sullivan, Li Zhou, Eric C Choy, Julia Chu
article en
7 citations

Abstract

Neuronal subtype generation in the mammalian central nervous system is governed by competing genetic programs. The medial ganglionic eminence (MGE) produces two major cortical interneuron (IN) populations, somatostatin (Sst) and parvalbumin (Pvalb), which develop on different timelines. The extent to which external signals influence these identities remains unclear. Pvalb-positive INs are crucial for cortical circuit regulation but challenging to model <i>in vitro</i>. We grafted mouse MGE progenitors into diverse 2D and 3D co-culture systems, including mouse and human cortical, MGE, and thalamic models. Strikingly, only 3D human corticogenesis models promoted efficient, non-autonomous Pvalb differentiation, characterized by upregulation of Pvalb maturation markers, downregulation of Sst-specific markers, and the formation of perineuronal nets. Additionally, lineage-traced postmitotic Sst-positive INs upregulated Pvalb when grafted onto human cortical models. These findings reveal unexpected fate plasticity in MGE-derived INs, suggesting that their identities can be dynamically shaped by the environment.

iScienceVol. 28(4)
University of California, San Francisco (US), University of California, Santa Cruz (US), Broad Center (US), Neurological Surgery (US)
National Science Foundation, California Institute for Regenerative Medicine, Office of the President, University of California, National Institute of Mental Health, National Human Genome Research Institute
Openalex Percentile: Top 3%
Genetics, Aging, and Longevity in Model Organisms
6.67
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