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RESEARCH PAPER / 2026-02-16

Local demyelination rekindles oligodendrocyte precursor dynamics and remyelination in old age

Eichenseer, K., Askari, S., Shkurti, L., Misgeld, T., Snaidero, N.

University of Tuebingen/ Hertie Institute of Clinical Brain Research · biorxiv

Abstract

Cortical myelination is critical for circuit function, plasticity, and long-term stability in the adult brain. With age and disease, the capacity to restore myelin after oligodendrocyte (OL) loss declines, and this failure is thought to reflect intrinsic limitations of OL precursor cells (OPCs) and a loss of permissive cues within the cortical environment. Here, using single-OL ablations and intravital imaging in mice, we show that as cortical remyelination efficiency declines, OPC motility declines, a phenomenon that can be mimicked by blocking CXCL12/CXCR4 signaling. Counter to prevailing notions, however, we find that even in aging, OPCs retain the capacity to generate new OLs and sheath axons, which can be rekindled by a graded demyelinating stimulus, inducing a more juvenile OPC motile state. This reveals an unrecognized remyelination potential in aging and identifies OPC dynamics as a key determinant of cortical remyelination, a property that could be targeted to improve myelin repair.

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Research summary

The paper claims that oligodendrocyte precursor cells retain the capacity for remyelination in aging, which can be enhanced by demyelination stimuli. This research addresses the mechanisms underlying myelin repair in aging, which is crucial for understanding and potentially mitigating age-related decline in brain function.

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