Pen-2 regulates glial homeostasis by coordinating self-renewal and transdifferentiation programs in oligodendrocyte
Huiru Bi1, Jinxing Hou2, Wenkai Shao3
1Department of Neurology, Nanjing Drum Tower Hospital, Affiliated Hospital of Nanjing University Medical School, Medical School, Nanjing University, Nanjing 210008, China; Nanjing Normal University of Special Education, Nanjing 210038, China.
Abstract:
Presenilin enhancer 2 (Pen-2) is implicated in neurological diseases characterized by glial dysregulation. To investigate whether oligodendrocytic γ-secretase activity is important for the maintenance of glial populations, we analyzed two conditional knockout (cKO) mouse models lacking Pen-2 or nicastrin. Both models exhibited similar expansions of oligodendrocyte precursor cells (OPCs) and astrocytes in the CNS. To test whether STAT3 mediates Pen-2-dependent glial homeostasis, we inactivated Stat3 in Pen-2 cKO mice. Intriguingly, STAT3 deficiency did not attenuate OPC expansion but normalized astrocyte numbers. We further demonstrated that Pen-2 represses Ascl1 expression via HES1 and that Ascl1 knockdown rescues the aberrant self-renewal capacity of Pen-2-deficient OPCs. Collectively, these results uncover a dual regulatory mechanism by which Pen-2 maintains glial homeostasis by (1) restraining OPC self-renewal through the HES1-ASCL1 axis and (2) suppressing OPC-to-astrocyte transdifferentiation in a STAT3-dependent manner. Our findings provide novel insights into glial abnormalities in PEN-2-linked neurological diseases.
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