Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Aug 11;11(16):2499.
doi: 10.3390/cells11162499.

Neurons: The Interplay between Cytoskeleton, Ion Channels/Transporters and Mitochondria

Affiliations
Review

Neurons: The Interplay between Cytoskeleton, Ion Channels/Transporters and Mitochondria

Paola Alberti et al. Cells. .

Abstract

Neurons are permanent cells whose key feature is information transmission via chemical and electrical signals. Therefore, a finely tuned homeostasis is necessary to maintain function and preserve neuronal lifelong survival. The cytoskeleton, and in particular microtubules, are far from being inert actors in the maintenance of this complex cellular equilibrium, and they participate in the mobilization of molecular cargos and organelles, thus influencing neuronal migration, neuritis growth and synaptic transmission. Notably, alterations of cytoskeletal dynamics have been linked to alterations of neuronal excitability. In this review, we discuss the characteristics of the neuronal cytoskeleton and provide insights into alterations of this component leading to human diseases, addressing how these might affect excitability/synaptic activity, as well as neuronal functioning. We also provide an overview of the microscopic approaches to visualize and assess the cytoskeleton, with a specific focus on mitochondrial trafficking.

Keywords: axonal excitability; biomarkers; cytoskeleton; ion channels; transporters.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Mitochondrial trafficking with holotomographic microscopy. Each panel (panel (AC)) enables us to follow different mitochondria at different time frames (time frame is stated in the upper left corner of each image). White arrows point out single mitochondria in each frame (images obtained with Nanolive holotomographic microscope).

References

    1. Marek K.W., Davis G.W. Controlling the active properties of excitable cells. Curr. Opin. Neurobiol. 2003;13:607–611. doi: 10.1016/j.conb.2003.09.001. - DOI - PubMed
    1. López-Bendito G., Arlotta P. Cell replacement therapies for nervous system regeneration. Dev. Neurobiol. 2012;72:145–152. doi: 10.1002/dneu.20897. - DOI - PMC - PubMed
    1. Frade J.M., Ovejero-Benito M.C. Neuronal cell cycle: The neuron itself and its circumstances. Cell Cycle. 2015;14:712–720. doi: 10.1080/15384101.2015.1004937. - DOI - PMC - PubMed
    1. Sheng Z.H. The Interplay of Axonal Energy Homeostasis and Mitochondrial Trafficking and Anchoring. Trends Cell Biol. 2017;27:403–416. doi: 10.1016/j.tcb.2017.01.005. - DOI - PMC - PubMed
    1. Sheng Z.H. Mitochondrial trafficking and anchoring in neurons: New insight and implications. J. Cell Biol. 2014;204:1087–1098. doi: 10.1083/jcb.201312123. - DOI - PMC - PubMed

LinkOut - more resources