Investigating the formation and remodelling of myelinated axons in vivo
dc.contributor.advisor
Lyons, David
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dc.contributor.advisor
Ffrench-Constant, Charles
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dc.contributor.author
Williamson, Jill M.
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dc.contributor.sponsor
Medical Research Council (MRC)
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dc.date.accessioned
2020-01-30T10:48:23Z
dc.date.available
2020-01-30T10:48:23Z
dc.date.issued
2020-01-22
dc.description.abstract
Myelin is a crucial component of the vertebrate nervous system, both in facilitating
rapid conduction of action potentials and in metabolically supporting axons. Recent
research has theorised that myelin sheaths play a more intricate role in nervous
system function by regulating circuits in response to experience. The number, length,
thickness, and distribution of myelin sheaths along an axon all influence its underlying
conduction properties. Thus, establishing or changing particular myelin patterns along
axons could refine the precise timing of signals to change circuit outputs. Yet, how
the myelin patterns along single axons are established, how myelin is remodelled over
time, and how neuronal activity affects these processes, is not yet fully understood. I
sought to investigate how myelin is formed, remodelled and maintained over time
along individual axons in the larval zebrafish central nervous system.
I first characterised the formation of myelin patterns along two different subtypes of
axon in the larval zebrafish spinal cord. Using transgenic tools and confocal
microscopy, I performed live imaging of single axons over a period of time during
developmental myelination. Reticulospinal (RS) axons are involved in locomotor
circuits, and are myelinated in a synaptic vesicle release-dependent manner;
whereas, Commissural Primary Ascending (CoPA) axons are involved in sensory
processing circuits, and are myelinated in a synaptic vesicle release-independent
manner. I hypothesised that myelin patterns along axons are formed in a circuit-dependent
fashion, and, therefore, that axons from different circuits would exhibit
different myelin patterns. However, I found that both RS and CoPA axons have very
similar myelin patterns, in terms of their myelin sheath number, length, myelin
coverage, and nodal gap length, and that these patterns are established within a
defined time window after the onset of myelination.
I, then, assessed how myelin sheaths are remodelled along RS and CoPA axons over
time, and found that myelin sheaths could either grow or shrink in length, or could be
fully retracted from the axon itself. I hypothesised that myelin remodelling would occur
along axons which use activity-related signals to regulate their myelination, and
therefore, that RS axons would exhibit more myelin remodelling than CoPA axons.
However, I found that RS and CoPA axons exhibited very similar degrees of myelin
remodelling.
Finally, I used a chemogenetic tool and live imaging by confocal microscopy to
investigate how increasing activity in individual RS axons affects the dynamics of
myelin sheath growth and the formation of myelin patterns. I found that increasing
neuronal activity promotes the early growth of myelin sheaths within a critical period;
after this period, neuronal activity no longer affects myelin sheath dynamics along RS
axons. By promoting this early sheath growth, activity can change the myelin pattern
established along individual RS axons.
Collectively, this research begins to elucidate how individual myelinated axons are
formed and maintained during nervous system development, and the cellular
mechanisms by which neuronal activity may regulate this process.
en
dc.identifier.uri
https://hdl.handle.net/1842/36699
dc.identifier.uri
http://dx.doi.org/10.7488/era/6
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
Almeida, R.G., Pan, S., Cole, K.L.H., Williamson, J.M., Early, J.J., Czopka, T., Klingseisen, A., Chan, J.R., Lyons, D.A., 2018. Myelination of neuronal cell bodies when myelin supply exceeds axonal demand. Curr. Biol. 28, 1296–1305.
en
dc.relation.hasversion
Early, J.J., Cole, K.L.H., Williamson, J.M., Swire, M., Kamadurai, H., Muskavitch, M., Lyons, D.A., 2018. An automated high-resolution in vivo screen in Zebrafish to identify chemical regulators of myelination. Elife 7, e35136.
en
dc.relation.hasversion
Williamson, J. M., and Lyons, D. A. (2018). Myelin dynamics throughout life: an ever-changing landscape? Front. Cell. Neurosci. 12. doi:10.3389/fncel.2018.00424.
en
dc.relation.hasversion
Williamson, J. M., Lyons, D. A., and Almeida, R. G. (2019). “Manipulating neuronal activity in the developing zebrafish spinal cord to investigate adaptive myelination,” in Oligodendrocytes: Methods and Protocols, eds D. A. Lyons and L. Kegel (New York, NY: Springer New York), 211-225. doi:10.1007/978- 1-4939-9072-6_12.
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dc.subject
myelin
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dc.subject
myelin sheaths
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dc.subject
zebrafish
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dc.subject
zebrafish spinal cord
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dc.subject
myelinated axons
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dc.subject
live imaging
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dc.subject
axons
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dc.subject
myelin sheath development
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dc.subject
CoPA
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dc.subject
CoPA axons
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dc.subject
RS axons
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dc.title
Investigating the formation and remodelling of myelinated axons in vivo
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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