Collateral Sprouting of Peripheral Sensory Neurons Exhibits a Unique Transcriptomic Profile
Author
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Lemaitre, Dominique
Author
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Llavero Hurtado, Maica
Author
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De Gregorio, Cristian
Author
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Oñate, Maritza G.
Author
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Martínez Bravo, Gabriela
Author
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Catenaccio, Alejandra
Author
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Wishart, Thomas M.
Author
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Court, Felipe A.
Admission date
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2020-09-21T16:29:01Z
Available date
dc.date.available
2020-09-21T16:29:01Z
Publication date
dc.date.issued
2020
Cita de ítem
dc.identifier.citation
Molecular Neurobiology 57(1): 4232-4249 (2020)
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Identifier
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10.1007/s12035-020-01986-3
Identifier
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https://repositorio.uchile.cl/handle/2250/176798
Abstract
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Peripheral nerve injuries result in motor and sensory dysfunction which can be recovered by compensatory or regenerative
processes. In situations where axonal regeneration of injured neurons is hampered, compensation by collateral sprouting from
uninjured neurons contributes to target reinnervation and functional recovery. Interestingly, this process of collateral sprouting from
uninjured neurons has been associated with the activation of growth-associated programs triggered by Wallerian degeneration.
Nevertheless, themolecular alterations at the transcriptomic level associated with these compensatory growthmechanisms remain to
be fully elucidated. We generated a surgical model of partial sciatic nerve injury in mice to mechanistically study degenerationinduced
collateral sprouting from spared fibers in the peripheral nervous system. Using next-generation sequencing and Ingenuity
Pathway Analysis, we described the sprouting-associated transcriptome of uninjured sensory neurons and compare it with the
activated by regenerating neurons. In vitro approacheswere used to functionally assess sprouting gene candidates in the mechanisms
of axonal growth. Using a novel animal model, we provide the first description of the sprouting transcriptome observed in uninjured
sensory neurons after nerve injury. This collateral sprouting-associated transcriptome differs from that seen in regenerating neurons,
suggesting a molecular program distinct from axonal growth.We further demonstrate that genetic upregulation of novel sproutingassociated
genes activates a specific growth program in vitro, leading to increased neuronal branching. These results contribute to
our understanding of the molecular mechanisms associated with collateral sprouting in vivo. The data provided here will therefore
be instrumental in developing therapeutic strategies aimed at promoting functional recovery after injury to the nervous system.
es_ES
Patrocinador
dc.description.sponsorship
Geroscience Center for Brain Health and Metabolism
FONDAP-15150012
Takeda Pharmaceutical Company Ltd
P09-015-F
Formation of Advance Human Capital Program of CONICYT
21110017
ISPG from the BBSRC
FONDECYT-1150766
FONDECYT1190518