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An isogenic human iPSC model unravels neurodevelopmental abnormalities in SMA

Grass, T.; Rosignol, I.; Thomas, J.; Buchner, F.; Dokuzluoglu, Z.; Dalinskaya, A.; Becker, J.; Wirth, B.; Rodriguez-Muela, N.

2023-01-03 neuroscience
10.1101/2023.01.02.522499 bioRxiv
Show abstract

Whether neurodevelopmental defects underlie the selective neuronal death that characterizes neurodegenerative diseases is becoming an intriguing question. To address it, we focused on the motor neuron (MN) disease Spinal Muscular Atrophy (SMA), caused by reduced levels of the ubiquitous protein SMN. Taking advantage of the first isogenic human induced pluripotent stem cell-derived SMA model that we have generated and a spinal cord organoid system, here we report that the relative and temporal expression of early neural progenitor and MN markers is altered in SMA. Furthermore, the corrected isogenic controls only partially reverse these abnormalities. These findings raise the relevant clinical implication that SMN-increasing treatments might not fully amend SMA pathological phenotypes. The approach we have taken demonstrates that the discovery of new disease mechanisms is greatly improved by using human isogenic models. Moreover, our study implies that SMA has a developmental component that might trigger the MN degeneration.

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