The neuron-intrinsic membrane skeleton is required for motor neuron integrity throughout lifespan

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The paper investigates whether the spectrin-based membrane periodic skeleton (MPS), specifically β-spectrin/UNC-70, is required for maintaining GABAergic motor neuron axon integrity in C. elegans across development and adulthood. Using an auxin-inducible degron system for cell-type–specific, time-dependent degradation of β-spectrin, the authors found that degrading β-spectrin from neurons beginning at larval stages caused widespread axon breakage and regeneration in VD/DD GABAergic motor neurons in both larvae and adults, and similar breakage occurred when degradation was restricted to GABA neurons or initiated from the mature nervous system. They also report that epidermal β-spectrin is not required for VD/DD axon integrity, highlighting a cell-intrinsic neuronal role. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Axons experience physical stress throughout an organism’s lifetime, and disruptions in axonal integrity are hallmarks of both neurodegenerative diseases and traumatic injuries. The spectrin-based membrane periodic skeleton (MPS) is proposed to have a crucial role in maintaining axonal strength, flexibility, and resilience. To investigate the importance of the intrinsic MPS for GABAergic motor neuron integrity in C. elegans , we employed the auxin-inducible degron system to degrade β-spectrin/UNC-70 in a cell-type specific and time-dependent manner. Degradation of β-spectrin from all neurons beginning at larval development resulted in widespread axon breakage and regeneration in VD/DD GABAergic motor neurons in both larval and adult animals. Similarly, targeted degradation of β-spectrin in GABA neurons alone resulted in extensive breakage. Moreover, we found that depleting β-spectrin from the mature nervous system also induced axon breaks. By contrast, epidermal β-spectrin was not required for axon integrity of VD/DD neurons. These findings demonstrate the cell-intrinsic importance of neuronal β-spectrin/UNC-70 for axon integrity both during development and in adulthood.
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Abstract Axons experience physical stress throughout an organism’s lifetime, and disruptions in axonal integrity are hallmarks of both neurodegenerative diseases and traumatic injuries. The spectrin-based membrane periodic skeleton (MPS) is proposed to have a crucial role in maintaining axonal strength, flexibility, and resilience. To investigate the importance of the intrinsic MPS for GABAergic motor neuron integrity in C. elegans, we employed the auxin-inducible degron system to degrade β-spectrin/UNC-70 in a cell-type specific and time-dependent manner. Degradation of β-spectrin from all neurons beginning at larval development resulted in widespread axon breakage and regeneration in VD/DD GABAergic motor neurons in both larval and adult animals. Similarly, targeted degradation of β-spectrin in GABA neurons alone resulted in extensive breakage. Moreover, we found that depleting β-spectrin from the mature nervous system also induced axon breaks. By contrast, epidermal β-spectrin was not required for axon integrity of VD/DD neurons. These findings demonstrate the cell-intrinsic importance of neuronal β-spectrin/UNC-70 for axon integrity both during development and in adulthood. Competing Interest Statement The authors have declared no competing interest. Footnotes ↵5 Lead Contact

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europepmc
last seen: 2026-05-20T01:45:00.602351+00:00