bioRxiv preprint doi: https://doi.org/10.1101/2020.03.06.981373; this version posted March 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Evidence for oligodendrocyte progenitor cell heterogeneity in the adult mouse brain. Authors: Rebecca M. Beiter1,2, Anthony Fernández-Castañeda1,2, Courtney Rivet-Noor1,2, Andrea Merchak1,2, Robin Bai1, Erica Slogar1, Scott M. Seki1,2,3, Dorian A Rosen1,4, Christopher C. Overall1,5, and Alban Gaultier1,5,# 1Center for Brain Immunology and Glia, Department of Neuroscience, 2Graduate Program in Neuroscience, 3Medical Scientist Training Program, 4Graduate Program in Pharmacological Sciences School of Medicine, University of Virginia, Charlottesville, VA 22908, USA. #Corresponding author. Email:
[email protected] 5Christopher C. Overall and Alban Gaultier are co-senior authors 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.03.06.981373; this version posted March 8, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. ABSTRACT Oligodendrocyte progenitor cells (OPCs) are a mitotically active population of glia that comprise approximately 5% of the adult brain. OPCs maintain their proliferative capacity and ability to differentiate in oligodendrocytes throughout adulthood, but relatively few mature oligodendrocytes are produced following developmental myelination. Recent work has begun to demonstrate that OPCs likely perform multiple functions in both homeostasis and disease, and can significantly impact behavioral phenotypes such as food intake and depressive symptoms. However, the exact mechanisms through which OPCs might influence brain function remains unclear.