Developmental and Regional Patterns of GAP-43 Immunoreactivity in a Metamorphosing Brain
Open accessAbstract
Growth-associated protein-43 is typically expressed at high levels in the nervous system during development. In adult animals, its expression is lower, but still observable in brain areas showing structural or functional plasticity. We examined patterns of GAP-43 immunoreactivity in the brain of the bullfrog, an animal whose nervous system undergoes considerable reorganization across metamorphic development and retains a strong capacity for plasticity in adulthood. Immunolabeling was mostly diffuse in hatchling tadpoles, but became progressively more discrete as larval development proceeded. In many brain areas, intensity of immunolabel peaked at metamorphic climax, the time of final transition from aquatic to semi-terrestrial life. Changes in intensity of GAP-43 expression in the medial vestibular nucleus, superior olivary nucleus, and torus semicircularis appeared correlated with stage-dependent functional changes in processing auditory stimuli. Immunolabeling in the Purkinje cell layer of the cerebellum and in the cerebellar nucleus was detectable at most developmental time points. Heavy immunolabel was present from early larval stages through the end of climax in the thalamus (ventromedial, anterior, posterior, central nuclei). Immunolabel in the tadpole telencephalon was observed around the lateral ventricles, and in the medial septum and ventral striatum. In postmetamorphic animals, immunoreactivity was confined mainly to the ventricular zones and immediately adjacent cell layers. GAP-43 expression was present in olfactory, auditory and optic cranial nerves throughout larval and postmetamorphic life. The continued expression of GAP-43 in brain nuclei and in cranial nerves throughout development and into adulthood reflects the high regenerative potential of the bullfrog’s central nervous system.
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GAP-43 is expressed in both the CNS and the ENS; it is found in high levels throughout the lifespan in the hippocampus, as well as in the myenteric and submucous ganglia.
“An important neurodevelopment and plasticity-related protein growth-associated protein-43 (GAP-43) is expressed in both the CNS and the ENS; it is found in high levels throughout the lifespan in the hippocampus (Simmons et al., 2008), as well as in the myenteric and submucous ganglia (Giaroni et al., 1999;Stewart et al., 1992).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Simmons et al., 2008
The ‘Species Similarities and Differences in GAP-43 Immunoreactivity’ section reports GAP-43’s presence in the mammalian hippocampus. It does not establish that hippocampal levels are high throughout the lifespan. The myenteric and submucous ganglia are cited to other sources in the citing sentence, not to Simmons et al.; page numbers were unavailable in our copy. (LLM, conf=0.85)
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Research works printed but not linked: 4
- McDiarmid RW, Altig R (1999) Research: mate- rials and techniques. In: Tadpoles: the Biol- ogy of Anuran Larvae (McDiarmid RW, Al- tig R, eds), pp 7-23. Chicago, IL: University of Chicago Press.
- Nieuwenhuys R, Opdam P (1976) Structure of the brain stem. In: Frog Neurobiology (Lli- nas R, Precht W, eds), pp 81-855. New York: Springer-Verlag.
- Shi Y-B (1999) Amphibian Metamorphosis: From Morphology to Molecular Biology. New York: Wiley-Liss.
- Simmons AM, Horowitz SS (2007) Plasticity in the auditory system across metamorphosis. In: Hearing and Sound Communication in Amphibians (Fay RR, Popper AN, Narins PM, Feng AS, eds), pp 291-322. New York: Springer-Verlag.
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Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works
- Authors
- Simmons, A. M., Tanyu, L. H., Horowitz, S. S., Chapman, J. A., & Brown, R. A.
- Affiliations
- Brown University (US)
- Venue
- Brain, Behavior and Evolution
- Publisher
- S. Karger AG
- Published
- 2008
- Volume
- 71
- Issue
- 4
- Pages
- 247-262
- ISSN
- 0006-8977 (ISSN-L)
- 1421-9743
- PMC
- PMC3257825
- OpenAlex
- W2059742898
- Cited by
- 9
- References
- 0
- Citations by year
- 2019: 1 · 2018: 2 · 2017: 1 · 2016: 1 · 2012: 1
- FWCI
- 0.31
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Brain Behavior and Evolution (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Rhode Island Space Grant Consortium
- National Institutes of Health
- National Institute on Deafness and Other Communication Disorders (F31DC006776, R01-DC05257, R01DC005257)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- growth-associated protein 43, brain development, metamorphosis, bullfrog, larval brain, metamorphic climax, auditory processing, vestibular nuclei, superior olivary nucleus, torus semicircularis, cerebellum, thalamus, telencephalon, cranial nerves, neuroplasticity, central nervous system regeneration, ventricular zone
- MeSH terms
- Animals, Brain, Immunohistochemistry, Larva, Medulla Oblongata, Mesencephalon, Metamorphosis, Biological, Neural Pathways, Rana catesbeiana, Biomarkers, Up-Regulation, GAP-43 Protein
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