Reprogramming of neuronal genome function and phenotype by astrocytes
Neuronal gene expression and chromatin accessibility landscape are profoundly remodeled by astrocytes over weeks of co-cultureAstrocyte-responsive neuronal gene modules and neuron-responsive astrocytic gene modules are enriched for genes associated with schizophrenia and familial Alzheimer's DiseaseSingle-cell CRISPR interference and activation screens of astrocyte-responsive gene regulatory elements identified dozens of functional regulatory elements of TF genes in neuronsSingle-cell CRISPR interference and activation screens of >200 astrocyte-responsive TF genes uncovered discrete functional clusters that promote neuronal maturity or stemnessAstrocyte-responsive TF genes reprogram neuronal electrophysiology and neurite morphology.
Authors
- Sara Geraghty (ORCID: https://orcid.org/0000-0002-6476-0207)
- Alexias Safi (ORCID: https://orcid.org/0000-0001-6381-4923)
- Kevin Hagy
- B. Li
- M Beer (ORCID: https://orcid.org/0000-0001-9955-3809)
- Ruhi Rai
- Samuel Reisman
- Cagla Eroglu
- Michael I. Love
- Patrick F. Sullivan
- Gregory E. Crawford
- Alyssa N. Pederson
- Charles A. Gersbach
Institutions
- University of North Carolina at Chapel Hill (US)
- Howard Hughes Medical Institute (US)
- Johns Hopkins University (US)
- Duke University (US)
- Duke Institute for Health Innovation (US)
- Duke Medical Center (US)
- Duke University Hospital (US)
- Applied Genetic Technologies (United States) (US)
Publication Details
- Journal
- bioRxiv (Cold Spring Harbor Laboratory)
- Published
- 2026-03-07
- DOI
- https://doi.org/10.64898/2026.03.07.710282
- Primary Topic
- Pluripotent Stem Cells Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00