Cited by 76Nerve injury and regenerationNeuropeptides and Animal PhysiologyCongenital gastrointestinal and neural anomalies

The DOI matches its Crossref record.

GAP-43 immunoreactivity is widespread in the autonomic neurons and sensory neurons of the rat

Stewart, H.J.S., Cowen, T., Curtis, R., Wilkin, G.P., Mirsky, R., Jessen, K.R.·1992·Neuroscience

Abstract

GAP-43 is a membrane-bound phosphoprotein generally associated with axon growth during development and regeneration. Using immunohistochemical and immunoblotting techniques this study shows that GAP-43 is expressed extensively in the unperturbed adult autonomic nervous system. Strong immunoreactivity was seen in the developing and mature enteric subdivision of the autonomic nervous system and in nerves of the iris and various blood vessels. The presence of GAP-43 immunoreactivity in varicose nerve fibres, and a comparison of the labelling pattern of GAP-43 with the nerve associated marker PGP 9.5 suggests that GAP-43 is present in most or all autonomic nerve fibres in these organs. Immunoblotting of gut samples on 10% polyacrylamide gels revealed a single band of approximately 45,000 mol. wt that co-migrated with pure central nervous system GAP-43. Surgical sympathectomy experiments resulting in almost complete elimination of sympathetic fibres did not markedly affect the pattern of GAP-43 immunoreactivity in the iris, indicating that GAP-43 is expressed not only in sympathetic nerves but also in parasympathetic and sensory fibres. These findings show that GAP-43 is expressed extensively in autonomic nerves of the adult rat, at levels comparable to those seen during development. High levels of GAP-43 are not therefore restricted to development and regeneration in this part of the nervous system.

Overview

Integrity signals

Registry

Crossref · 10.1016/0306-4522(92)90175-2

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • 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 Stewart et al., 1992

Citations

Cites

No references could be resolved yet.

Research works printed but not linked: 46

  1. Anderton, 1982, Monoclonal antibodies show that neurofibrillary tangles and neurofilaments share antigenic determinants, Nature, 298, 84, 10.1038/298084a0 · DOI
  2. Benowitz, 1987, A membrane phosphoprotein associated with neural development, axonal regeneration, phospholipid metabolism, and synaptic plasticity, Trends Neurosci., 10, 527, 10.1016/0166-2236(87)90135-4 · DOI
  3. Benowitz, 1988, Anatomical distribution of the growth-associated protein GAP-43/B-50 in the adult rat brain, J. Neurosci., 8, 339, 10.1523/JNEUROSCI.08-01-00339.1988 · DOI
  4. Benowitz, 1989, Localization of the growth associated protein GAP-43 (B50,F1) in the human cerebral cortex, J. Neurosci., 9, 990, 10.1523/JNEUROSCI.09-03-00990.1989 · DOI
  5. Burnstock, 1971, Fine structural identification of autonomic nerves and their relation to smooth muscle, Vol. 34, 389
  6. Chan, 1986, Phosphoprotein F1: purification and characterization of a brain kinase C substrate related to plasticity, J. Neurosci., 6, 3618, 10.1523/JNEUROSCI.06-12-03618.1986 · DOI
  7. Cowen, 1985, Pontamine sky blue: a counterstain for background autofluorescence in fluorescence and histochemistry, Histochemistry, 82, 205, 10.1007/BF00501396 · DOI
  8. Curtis, 1991, Down-regulation of GAP-43 during oligodendrocyte development and lack of expression by astrocytes in vivo: implications for macroglial differentiation, Eur. J. Neurosci., 3, 876, 10.1111/j.1460-9568.1991.tb00099.x · DOI
  9. Curtis, 1992, Gap-43 is expressed by non-myelin-forming Schwann cells of the peripheral nervous system, J. Cell Biol., 10.1083/jcb.116.6.1455 · DOI
  10. Da Cunha, 1990, Regulation of immunoreactive GAP-43 expression in the rat cortical macroglia is cell type specific, J. Cell Biol., 111, 209, 10.1083/jcb.111.1.209 · DOI
  11. De La Monte, 1989, GAP-43 gene expression during development: persistence in a distinctive set of neurones in the mature central nervous system, Devl Brain Res., 46, 161, 10.1016/0165-3806(89)90279-4 · DOI
  12. De La Torre, 1976, A methodological approach to rapid and sensitive monoamine histofluorescence using a modified glyoxylic acid technique, the SPG method, Histochemistry, 49, 81, 10.1007/BF00495672 · DOI
  13. Deloulme, 1990, Neuromodulin (GAP-43): a neuronal protein kinase C substrate is also present in 0-2A glial cell lineage. Characterization of neuromodulin in secondary cultures of oligodendrocytes and comparison with the neuronal antigen, J. Cell Biol., 111, 1559, 10.1083/jcb.111.4.1559 · DOI
  14. Doster, 1991, Expression of the growth-associated protein GAP-43 in adult rat retinal ganglion cells following axonal injury, Neuron, 6, 635 647, 10.1016/0896-6273(91)90066-9 · DOI
  15. Gabella, 1989, Size of neurones and glial cells in the intramural ganglia of the hypertrophic intestine of the Guinea pig, J. Neurocytol., 13, 73, 10.1007/BF01148319 · DOI
  16. Gabella, 1984, Size of neurones and glial cells in the enteric ganglia of mice, guinea pigs, rabbits and sheep, J. Neurocytol., 13, 49, 10.1007/BF01148318 · DOI
  17. Goslin, 1988, Development of neuronal polarity: GAP-43 distinguishes axonal from dendritic growth, Nature, 336, 672, 10.1038/336672a0 · DOI
  18. Grabczyk, 1990, Cloning and characterization of the rat gene encoding GAP-43, Eur. J. Neurosci., 2, 822, 10.1111/j.1460-9568.1990.tb00393.x · DOI
  19. Greenberg, 1990, Irregular geometries in normal unmyelinated axons: a 3D serial EM analysis, J. Neurocytol., 19, 978, 10.1007/BF01186825 · DOI
  20. Gulbenkian, 1987, The visualization of cardiovascular innervation in the guinea pig using an antiserum to protein gene product 9.5 (PGP 9.5), J. auton. nerv. Syst., 18, 235, 10.1016/0165-1838(87)90122-6 · DOI
  21. Hoffman, 1989, Expression of GAP-43, a rapidly transported growth-associated protein, and class II beta tubulin, a slowly transported cytoskeletal protein, are coordinated in regenerating neurones, J. Neurosci., 9, 893, 10.1523/JNEUROSCI.09-03-00893.1989 · DOI
  22. Kessler, 1985, Parasympathetic, sympathetic, and sensory interactions in the iris: nerve growth factor regulates cholinergic ciliary ganglion innervation in vivo, J. Neurosci., 5, 2719, 10.1523/JNEUROSCI.05-10-02719.1985 · DOI
  23. Kessler, 1983, Interactions between the sympathetic and sensory innervation of the iris, J. Neurosci., 3, 1301, 10.1523/JNEUROSCI.03-06-01301.1983 · DOI · Paper page
  24. Laemmli, 1970, Cleavage of structural proteins during the assembly of the head of bacteriophage T4, Nature, 227, 680, 10.1038/227680a0 · DOI · Paper page
  25. Lawson, 1984, A monoclonal antibody against neurofilament protein specifically labels a subpopulation of rat sensory neurones, J. comp. Neurol., 228, 263, 10.1002/cne.902280211 · DOI
  26. Lichtman, 1987, Visualization of neuromuscular junctions over periods of several months in living mice, J. Neurosci., 7, 1215, 10.1523/JNEUROSCI.07-04-01215.1987 · DOI
  27. McGuire, 1988, Light microscopic immunolocalization of the growth- and plasticity-associated protein GAP-43 in the developing rat brain, Devl Brain Res., 41, 277, 10.1016/0165-3806(88)90189-7 · DOI
  28. Meiri, 1990, GAP-43 in growth cones is associated with areas of membrane that are tightly bound to substrate and is a component of a membrane skeleton subcellular fraction, J. Neurosci., 10, 256, 10.1523/JNEUROSCI.10-01-00256.1990 · DOI
  29. Moss, 1990, Chicken growth-associated protein GAP-43 is tightly bound to the actin-rich neuronal membrane skeleton, J. Neurochem., 54, 729, 10.1111/j.1471-4159.1990.tb02312.x · DOI
  30. Neve, 1987, The neuronal growth associated protein GAP-43 (B50, F1): neuronal specificity, developmental regulation and regional distribution of the human and rat mRNAs, Molec Brain Res., 2, 177, 10.1016/0169-328X(87)90012-X · DOI
  31. Purves, 1987, Nerve terminal remodelling visualized in living mice by repeated examination of the same neurone, Science, 238, 1122, 10.1126/science.3685967 · DOI
  32. Purves, 1987, Imaging mammalian nerve cells and their connections over time in living animals, Trends Neurosci., 10, 398, 10.1016/0166-2236(87)90005-1 · DOI
  33. Roth, 1969, Electron microscopic studies on axonal degeneration in the rat iris following ganglionectomy, Am. J. Anat., 124, 341, 10.1002/aja.1001240305 · DOI
  34. Sharkey, 1990, Distribution of growth-associated protein B-50 (GAP-43) in the mammalian enteric nervous system, Neuroscience, 38, 13, 10.1016/0306-4522(90)90370-J · DOI
  35. Skene, 1981, Characteristics of growth-associated polypeptides in regenerating toad retinal ganglion cell axons, J. Neurosci., 1, 419, 10.1523/JNEUROSCI.01-04-00419.1981 · DOI
  36. Skene, 1981, Changes in axonally transported proteins during axon regeneration in toad retinal ganglion cells, J. Cell Biol., 89, 86, 10.1083/jcb.89.1.86 · DOI
  37. Skene, 1981, Axonally transported proteins associated with axon growth in rabbit central and peripheral nervous systems, J. Cell Biol., 89, 96, 10.1083/jcb.89.1.96 · DOI
  38. Skene, 1989, Axonal growth-associated proteins, A. Rev. Neurosci., 12, 127, 10.1146/annurev.ne.12.030189.001015 · DOI
  39. Snipes, 1987, Regulation of specific neuronal and nonneuronal proteins during development and following injury in the rat central nervous system, Prog. Brain Res., 71, 155, 10.1016/S0079-6123(08)61821-X · DOI
  40. Tetzlaff, 1989, Axonal transport and localization of B50/GAP-43-like immunoreactivity in regenerating sciatic and facial nerves of the rat, J. Neurosci., 9, 1303, 10.1523/JNEUROSCI.09-04-01303.1989 · DOI
  41. Thompson, 1983, PGP 9.5—a new marker for vertebrate neurones and neuroendocrine cells, Brain Res., 278, 224, 10.1016/0006-8993(83)90241-X · DOI
  42. Verge, 1990, Correlation between GAP43 and nerve growth factor receptor in rat sensory neurones, J. Neurosci., 10, 926, 10.1523/JNEUROSCI.10-03-00926.1990 · DOI
  43. Verhaagen, 1990, B-50/GAP-43 gene expression in the rat olfactory system during postnatal development and ageing, Eur. J. Neurosci., 2, 397, 10.1111/j.1460-9568.1990.tb00432.x · DOI
  44. Voyvodic, 1989, Peripheral target regulation of dendritic geometry in the rat superior cervical ganglion, J. Neurosci., 9, 1997, 10.1523/JNEUROSCI.09-06-01997.1989 · DOI
  45. Woolf, 1990, The growth-associated protein GAP-43 appears in the dorsal root ganglion cells and in the dorsal horn of the rat spinal cord following peripheral nerve injury, Neuroscience, 34, 465, 10.1016/0306-4522(90)90155-W · DOI
  46. Yamamoto, 1990, Gene expression of a neuronal growth-associated protein, GAP-43, in the paraganglionic carotid body as well as in the autonomic ganglia of normal adult rats, Neurosci. Lett., 117, 275, 10.1016/0304-3940(90)90676-Z · DOI

Cited by

Sorted by citations

Metadata

Authors
Stewart, H. J. S., Cowen, T., Curtis, R., Wilkin, G. P., Mirsky, R., & Jessen, K. R.
Affiliations
  • University College London (GB)
  • Imperial College London (GB)
  • The Royal Free Hospital (GB)
Corresponding author
Stewart, H.J.S.
Venue
Neuroscience
Publisher
Elsevier BV
Published
1992-04
Volume
47
Issue
3
Pages
673-684
ISSN
0306-4522 (ISSN-L)
OpenAlex
W1988843477
Cited by
76
References
0
Citations by year
2020: 1 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 1 · 2014: 1 · 2012: 2
FWCI
3.23
Type
journal article
Language
en
Open access
closed
Locations
  • Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
Funders
Wellcome Trust
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
  • Health Sciences › Medicine › Surgery › Congenital gastrointestinal and neural anomalies
Keywords
GAP-43, neurofilaments, autonomic nervous system, enteric nervous system, sensory neurons, sympathetic nerves, parasympathetic nerves, varicose nerve fibers, PGP 9.5, sympathectomy, axon growth, adult nervous system
MeSH terms
Animals, Autonomic Nervous System, Catecholamines, Cholinergic Fibers, Electrophoresis, Polyacrylamide Gel, Immunohistochemistry, Male, Membrane Glycoproteins, Myenteric Plexus, Nerve Tissue Proteins, Neurons, Neurons, Afferent, Phosphoproteins, Rats, Inbred Strains, Sympathectomy, Blotting, Northern, GAP-43 Protein, Rats

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review