Changes in microtubule number and length during axon differentiation
Open accessAbstract
Hippocampal neurons in culture initially extend several minor processes that are approximately 20 microns in length. The first minor process to grow approximately 10 microns longer than the others will continue to grow rapidly and become the axon (Goslin and Banker, 1989). We sought to define changes in the microtubule (MT) array that occur during axon differentiation. In theory, axon differentiation could involve an increase in MT number, MT length, or some combination of both. To address this issue, we first serially reconstructed the entire MT array of a minor process from a cell whose axon had not yet differentiated. This minor process contained 182 MTs that ranged in length from 0.14 to 20.09 microns. The average MT length was 3.87 +/- 3.83 microns, and the total MT length was 704 microns. We then reconstructed the MT arrays of a minor process and the 56 microns axon from a cell that had undergone axon differentiation. The minor process contained 157 MTs that ranged in length from 0.24 to 17.95 microns. The average MT length was 3.91 +/- 4.84 microns, and the total MT length was 600 microns. The axon contained 1430 MTs that ranged in length from 0.05 to 40.14 microns. The average MT length was 4.02 +/- 5.28 microns, and the total MT length was 5750 microns. These data indicate that a shift occurs toward shorter as well as longer MTs, but that virtually no change in average MT length occurs during axon differentiation. Thus, elongation of existing MTs cannot account for the major expansion of the MT array that occurs as a minor process becomes an axon. In contrast, the number of MTs increases by approximately 10-fold as a minor process differentiates and grows into an axon of the length we analyzed. Based on these data, we conclude that the MT array of a minor process is substantially expanded as it differentiates into an axon, and that the principal mechanism by which this expansion occurs is the copious addition of new MTs.
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Limited spacing between MTs may block mitochondrial movement in neuritic processes such as axons and dendrites.
“Considering that mitochondria would be transported within MT bundles in cultured neurons (Yu and Baas, 1994;Rochlin et al., 1996), limited spacing between MTs may block mitochondrial movement in neuritic processes such as axon and dendrites.”
From Regulation of Mitochondrial Transport and Inter-Microtubule Spacing by Tau Phosphorylation at the Sites Hyperphosphorylated in Alzheimer's Disease (2012) · cites this paper as Yu and Baas, 1994
The axoplasmic MT milieu is under strong tension.
“These features may indicate that the axoplasmic MT milieu is under the strong tension (Yu and Baas, 1994;Rochlin et al., 1996).”
From Regulation of Mitochondrial Transport and Inter-Microtubule Spacing by Tau Phosphorylation at the Sites Hyperphosphorylated in Alzheimer's Disease (2012) · cites this paper as Yu and Baas, 1994
The Results and Discussion describe closely spaced, parallel axonal microtubules, but do not say that the axoplasmic microtubule milieu is under strong tension. Searches for tension and mechanical stress found no passage addressing that claim; page numbers were not available in our copy. (LLM, conf=0.74)
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Kosik, K., & Finch, E. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-10-03142.1987 · Cited by 368 · see citing works
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Research works printed but not linked: 2
- Banker G, Goslin K (1991) Characterizing and studying neuronal cultures. In: Culturing nerve cells (Banker G, Goslin K, eds), pp 75- 109. Cambridge, MA: MIT Press.
- Goslin K, Banker G (199 1) Rat hippocampal neurons in low-density culture. In: Culturing nerve cells (Banker G, Goslin K, eds), pp 251- 28 1. Cambridge, MA: MIT Press.
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Orchestrated reduction of quantum coherence in brain microtubules: a model for consciousness
Hameroff, S., & Penrose, R. (1996) · Mathematics and Computers in Simulation · doi:10.1016/0378-4754(96)80476-9 · Cited by 641 · see citing works
Axonal transport: Driving synaptic function
Guedes-Dias, P., & Holzbaur, E. L. F. (2019) · Science · doi:10.1126/science.aaw9997 · Cited by 355 · see citing works
Quantum computation in brain microtubules: decoherence and biological feasibility
Hagan, S., Hameroff, S. R., & Tuszyński, J. A. (2002) · Physical Review E · doi:10.1103/physreve.65.061901 · Cited by 389 · see citing works
An Essential Role for Katanin in Severing Microtubules in the Neuron
Ahmad, F. J., Yu, W., McNally, F. J., & Baas, P. W. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.2.305 · Cited by 253 · see citing works
Self-citationShahpasand, K., Uemura, I., Saito, T., Asano, T., Hata, K., Shibata, K., Toyoshima, Y., Hasegawa, M., & Hisanaga, S.-I. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5927-11.2012 · Cited by 206 · see citing works
Microtubules released from the neuronal centrosome are transported into the axon
Ahmad, F. J., & Baas, P. W. (1995) · Journal of Cell Science · doi:10.1242/jcs.108.8.2761 · Cited by 132 · see citing works
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- Authors
- Yu, W., & Baas, P.
- Affiliations
- University of Wisconsin System (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1994-05-01
- Volume
- 14
- Issue
- 5
- Pages
- 2818-2829
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6577472
- OpenAlex
- W2146640900
- Cited by
- 213
- References
- 1
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 3 · 2023: 8 · 2022: 11 · 2021: 8 · 2020: 14 · 2019: 9 · 2018: 10 · 2017: 10 · 2016: 11 · 2015: 17 · 2014: 3 · 2013: 8 · 2012: 2
- FWCI
- 2.37
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation (9209939)
- National Institutes of Health (28785)
- National Institute of Neurological Disorders and Stroke (NS-28785)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- microtubules, microtubule length, hippocampal neurons, axon growth, neuronal cytoskeleton
- MeSH terms
- Animals, Axons, Cell Differentiation, Cells, Cultured, Embryo, Mammalian, Hippocampus, Microscopy, Electron, Microtubules, Models, Structural, Neurons, Rats
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