Multiple sclerosis iPSC-derived oligodendroglia conserve their intrinsic properties to functionally interact with axons and glia in vivo

Mozafari, S.; Starost, L.; Manot-Saillet, B.; Garcia-Diaz, B.; Xu, Y. K. T.; Roussel, D.; Levy, M. J. F.; Ottoboni, L.; Kim, K.-P.; Scholer, H. R.; Kennedy, T. E.; Antel, J. P.; Martino, G.; Angulo, M. C.; Kuhlmann, T.; Baron-Van Evercooren, A.

doi:10.1101/2020.05.05.078642

bioRxiv · 10.1101/2020.05.05.078642

Multiple sclerosis iPSC-derived oligodendroglia conserve their intrinsic properties to functionally interact with axons and glia in vivo

Mozafari, S.·Starost, L.·Manot-Saillet, B.·Garcia-Diaz, B.·Xu, Y. K. T.·Roussel, D.·Levy, M. J. F.·Ottoboni, L.·Kim, K.-P.·Scholer, H. R.·Kennedy, T. E.·Antel, J. P.·Martino, G.·Angulo, M. C.·Kuhlmann, T.·Baron-Van Evercooren, A.

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Abstract

The remyelination failure in multiple sclerosis (MS) is associated with a migration/differentiation block of oligodendroglia. The reason for this block is highly debated. It could result from disease-related extrinsic regulators of the oligodendroglial biology or reflect MS oligodendrocyte intrinsic properties. To avoid confounding immune-mediated extrinsic effect, we used an immune-deficient, dysmyelinating mouse model, to compare side-by-side induced pluripotent stem-cell-derived O4+ oligodendroglia from MS and healthy donors following their engraftment in the developing CNS. We show that the MS-progeny survives, proliferates and differentiates into oligodendrocytes to the same extent as controls. Quantitative multi-parametric imaging indicates that MS and control oligodendrocytes generate equal amounts of myelin, with bona-fide nodes of Ranvier and promote equal restoration of their host slow conduction. Moreover, the MS-derived progeny expressed oligodendrocyte- and astrocyte-specific connexins and established functional connections with donor and host glial cells. Thus, MS pluripotent stem cell-derived progeny fully integrates into functional axo-glial and glial-glial components, reinforcing the view that the MS oligodendrocyte differentiation block is not due to intrinsic oligodendroglial deficits. These biological findings as well as the fully integrated human-murine chimeric model should facilitate the development of pharmacological or cell-based therapies to promote CNS remyelination. One Sentence SummaryMultiple Sclerosis oligodendroglia, regardless of major immune manipulators, are intrinsically capable of myelination and making functional axo-glia and glia-glia connections after engraftment in the murine CNS, reinforcing the view that the MS oligodendrocyte differentiation block is not due to major intrinsic oligodendroglial deficits but most likely to environmental conditions.

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Mozafari, S., Starost, L., Manot-Saillet, B., Garcia-Diaz, B., Xu, Y. K. T., Roussel, D., Levy, M. J. F., Ottoboni, L., Kim, K.-P., Scholer, H. R., Kennedy, T. E., Antel, J. P., Martino, G., Angulo, M. C., Kuhlmann, T., Baron-Van Evercooren, A.. 2020-05-06. Multiple sclerosis iPSC-derived oligodendroglia conserve their intrinsic properties to functionally interact with axons and glia in vivo. https://doi.org/10.1101/2020.05.05.078642

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