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Formin Activity and mDia1 Contribute to Maintain Axon Initial Segment Composition and Structure
- Source :
- Molecular Neurobiology, Molecular Neurobiology, 2021, ⟨10.1007/s12035-021-02531-6⟩, Digital.CSIC. Repositorio Institucional del CSIC, instname, Molecular Neurobiology, Humana Press, 2021, ⟨10.1007/s12035-021-02531-6⟩
- Publication Year :
- 2021
- Publisher :
- Springer Science and Business Media LLC, 2021.
-
Abstract
- The axon initial segment (AIS) is essential for maintaining neuronal polarity, modulating protein transport into the axon, and action potential generation. These functions are supported by a distinctive actin and microtubule cytoskeleton that controls axonal trafficking and maintains a high density of voltage-gated ion channels linked by scaffold proteins to the AIS cytoskeleton. However, our knowledge of the mechanisms and proteins involved in AIS cytoskeleton regulation to maintain or modulate AIS structure is limited. In this context, formins play a significant role in the modulation of actin and microtubules. We show that pharmacological inhibition of formins modifies AIS actin and microtubule characteristics in cultured hippocampal neurons, reducing F-actin density and decreasing microtubule acetylation. Moreover, formin inhibition diminishes sodium channels, ankyrinG and ßIV-spectrin AIS density, and AIS length, in cultured neurons and brain slices, accompanied by decreased neuronal excitability. We show that genetic downregulation of the mDia1 formin by interference RNAs also decreases AIS protein density and shortens AIS length. The ankyrinG decrease and AIS shortening observed in pharmacologically inhibited neurons and neuron-expressing mDia1 shRNAs were impaired by HDAC6 downregulation or EB1-GFP expression, known to increase microtubule acetylation or stability. However, actin stabilization only partially prevented AIS shortening without affecting AIS protein density loss. These results suggest that mDia1 maintain AIS composition and length contributing to the stability of AIS microtubules.<br />Open Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. The work was supported by agrant from Ministerio de Ciencia y Universidades (RTI2018-095156-B-100) to JJG and INSERM funding to DD. Wei Zhang was supported by a fellowship from China Scholarship Council (No.201506300085) and Beatriz Achon by a Master fellowship from Universidad Autónoma de Madrid.
- Subjects :
- Neuroscience (miscellaneous)
Formins
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
macromolecular substances
Hippocampus
Microtubules
Article
Mice
03 medical and health sciences
Cellular and Molecular Neuroscience
0302 clinical medicine
AnkyrinG
Microtubule
mDia1
medicine
Animals
Axon
Cytoskeleton
Cells, Cultured
Actin
030304 developmental biology
Neurons
0303 health sciences
biology
Chemistry
Sodium channel
Axon initial segment
Axons
Cell biology
medicine.anatomical_structure
Neurology
biology.protein
MDia1
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 15591182 and 08937648
- Volume :
- 58
- Database :
- OpenAIRE
- Journal :
- Molecular Neurobiology
- Accession number :
- edsair.doi.dedup.....d48fd22dac612831af9667dacc1b1546