Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta

Moran, David Taylor ; Rowley, J. Carter ; Aiken, George R. ; Jafek, Bruce W.

New York, NY [u.a.] : Wiley-Blackwell
Published 1992
ISSN:
1059-910X
Keywords:
Nose ; Olfaction ; Ultrastructure ; Toxicology ; Smell ; Sensory ; Fish ; Life and Medical Sciences ; Cell & Developmental Biology
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Natural Sciences in General
Notes:
This paper describes four investigations of the olfactory mucosa of the brown trout: 1) the ultrastructure of the olfactory mucosa as revealed by scanning (SEM), conventional transmission (TEM), and high voltage (HVEM) electron microscopy; 2) light and electron-microscopic investigations of retrograde transport of the tracer macromolecule horseradish peroxidase (HRP) when applied to the cut olfactory nerve; 3) SEM and TEM investigations of the effects of olfactory nerve transection on cell populations within the olfactory epithelium; and 4) ultrastructural investigations of reversible degeneration of olfactery receptors caused by elevated copper concentrations. The trout lofactory epithelium contains five cell types: ciliated epithelial cells, ciliated olfactory receptor cells, microvillar olfactory receptor cells, supporting cells, and basal cells. The ciliated and microvillar olfactory receptor cells and a small number of basal cells are backfilled by HRP when the tracer is applied to the cut olfactory nerve. When the olfactory nerve is cut, both ciliated and microvillar olfactory receptor cells degenerate within 2 days and are morphologically intact again within 8 days. When wild trout are taken from their native stream and placed in tanks with elevated copper concentrations, ciliated and microvillar cells degenerate. Replacement of these trout into their stream of origin is followed by morphologic restoration of both types of olfactory receptor cells. Ciliated and microvillar receptor cells are primary sensory bipolar neurons whose dendrites make contact with the environment; their axons travel directly to the brain. Consequently, substances can be transported directly from the environment into the brain via these “naked neurons.” Since fish cannot escape from the water in which they swim, and since that water may occasionally contain brain-toxic substances, the ability to close off - and later reopen - this anatomic gateway to the brain would confer a tremendous selective advantage upon animals that evolved the “brain-sparing” capacity to do so. Consequently, the unique regenerative powers of vertebrate olfactory receptor neurons may have their evolutionary origin in fishes. © 1992 Wiley-Liss, Inc.
Additional Material:
26 Ill.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297776849682432
addmaterial 26 Ill.
autor Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
autorsonst Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
book_url http://dx.doi.org/10.1002/jemt.1070230104
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM160586356
issn 1059-910X
journal_name Microscopy Research and Technique
materialart 1
notes This paper describes four investigations of the olfactory mucosa of the brown trout: 1) the ultrastructure of the olfactory mucosa as revealed by scanning (SEM), conventional transmission (TEM), and high voltage (HVEM) electron microscopy; 2) light and electron-microscopic investigations of retrograde transport of the tracer macromolecule horseradish peroxidase (HRP) when applied to the cut olfactory nerve; 3) SEM and TEM investigations of the effects of olfactory nerve transection on cell populations within the olfactory epithelium; and 4) ultrastructural investigations of reversible degeneration of olfactery receptors caused by elevated copper concentrations. The trout lofactory epithelium contains five cell types: ciliated epithelial cells, ciliated olfactory receptor cells, microvillar olfactory receptor cells, supporting cells, and basal cells. The ciliated and microvillar olfactory receptor cells and a small number of basal cells are backfilled by HRP when the tracer is applied to the cut olfactory nerve. When the olfactory nerve is cut, both ciliated and microvillar olfactory receptor cells degenerate within 2 days and are morphologically intact again within 8 days. When wild trout are taken from their native stream and placed in tanks with elevated copper concentrations, ciliated and microvillar cells degenerate. Replacement of these trout into their stream of origin is followed by morphologic restoration of both types of olfactory receptor cells. Ciliated and microvillar receptor cells are primary sensory bipolar neurons whose dendrites make contact with the environment; their axons travel directly to the brain. Consequently, substances can be transported directly from the environment into the brain via these “naked neurons.” Since fish cannot escape from the water in which they swim, and since that water may occasionally contain brain-toxic substances, the ability to close off - and later reopen - this anatomic gateway to the brain would confer a tremendous selective advantage upon animals that evolved the “brain-sparing” capacity to do so. Consequently, the unique regenerative powers of vertebrate olfactory receptor neurons may have their evolutionary origin in fishes. © 1992 Wiley-Liss, Inc.
package_name Wiley-Blackwell
publikationsjahr_anzeige 1992
publikationsjahr_facette 1992
publikationsjahr_intervall 8009:1990-1994
publikationsjahr_sort 1992
publikationsort New York, NY [u.a.]
publisher Wiley-Blackwell
reference 23 (1992), S. 28-48
schlagwort Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
search_space articles
shingle_author_1 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
shingle_author_2 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
shingle_author_3 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
shingle_author_4 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
shingle_catch_all_1 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
This paper describes four investigations of the olfactory mucosa of the brown trout: 1) the ultrastructure of the olfactory mucosa as revealed by scanning (SEM), conventional transmission (TEM), and high voltage (HVEM) electron microscopy; 2) light and electron-microscopic investigations of retrograde transport of the tracer macromolecule horseradish peroxidase (HRP) when applied to the cut olfactory nerve; 3) SEM and TEM investigations of the effects of olfactory nerve transection on cell populations within the olfactory epithelium; and 4) ultrastructural investigations of reversible degeneration of olfactery receptors caused by elevated copper concentrations. The trout lofactory epithelium contains five cell types: ciliated epithelial cells, ciliated olfactory receptor cells, microvillar olfactory receptor cells, supporting cells, and basal cells. The ciliated and microvillar olfactory receptor cells and a small number of basal cells are backfilled by HRP when the tracer is applied to the cut olfactory nerve. When the olfactory nerve is cut, both ciliated and microvillar olfactory receptor cells degenerate within 2 days and are morphologically intact again within 8 days. When wild trout are taken from their native stream and placed in tanks with elevated copper concentrations, ciliated and microvillar cells degenerate. Replacement of these trout into their stream of origin is followed by morphologic restoration of both types of olfactory receptor cells. Ciliated and microvillar receptor cells are primary sensory bipolar neurons whose dendrites make contact with the environment; their axons travel directly to the brain. Consequently, substances can be transported directly from the environment into the brain via these “naked neurons.” Since fish cannot escape from the water in which they swim, and since that water may occasionally contain brain-toxic substances, the ability to close off - and later reopen - this anatomic gateway to the brain would confer a tremendous selective advantage upon animals that evolved the “brain-sparing” capacity to do so. Consequently, the unique regenerative powers of vertebrate olfactory receptor neurons may have their evolutionary origin in fishes. © 1992 Wiley-Liss, Inc.
1059-910X
1059910X
Wiley-Blackwell
shingle_catch_all_2 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
This paper describes four investigations of the olfactory mucosa of the brown trout: 1) the ultrastructure of the olfactory mucosa as revealed by scanning (SEM), conventional transmission (TEM), and high voltage (HVEM) electron microscopy; 2) light and electron-microscopic investigations of retrograde transport of the tracer macromolecule horseradish peroxidase (HRP) when applied to the cut olfactory nerve; 3) SEM and TEM investigations of the effects of olfactory nerve transection on cell populations within the olfactory epithelium; and 4) ultrastructural investigations of reversible degeneration of olfactery receptors caused by elevated copper concentrations. The trout lofactory epithelium contains five cell types: ciliated epithelial cells, ciliated olfactory receptor cells, microvillar olfactory receptor cells, supporting cells, and basal cells. The ciliated and microvillar olfactory receptor cells and a small number of basal cells are backfilled by HRP when the tracer is applied to the cut olfactory nerve. When the olfactory nerve is cut, both ciliated and microvillar olfactory receptor cells degenerate within 2 days and are morphologically intact again within 8 days. When wild trout are taken from their native stream and placed in tanks with elevated copper concentrations, ciliated and microvillar cells degenerate. Replacement of these trout into their stream of origin is followed by morphologic restoration of both types of olfactory receptor cells. Ciliated and microvillar receptor cells are primary sensory bipolar neurons whose dendrites make contact with the environment; their axons travel directly to the brain. Consequently, substances can be transported directly from the environment into the brain via these “naked neurons.” Since fish cannot escape from the water in which they swim, and since that water may occasionally contain brain-toxic substances, the ability to close off - and later reopen - this anatomic gateway to the brain would confer a tremendous selective advantage upon animals that evolved the “brain-sparing” capacity to do so. Consequently, the unique regenerative powers of vertebrate olfactory receptor neurons may have their evolutionary origin in fishes. © 1992 Wiley-Liss, Inc.
1059-910X
1059910X
Wiley-Blackwell
shingle_catch_all_3 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
This paper describes four investigations of the olfactory mucosa of the brown trout: 1) the ultrastructure of the olfactory mucosa as revealed by scanning (SEM), conventional transmission (TEM), and high voltage (HVEM) electron microscopy; 2) light and electron-microscopic investigations of retrograde transport of the tracer macromolecule horseradish peroxidase (HRP) when applied to the cut olfactory nerve; 3) SEM and TEM investigations of the effects of olfactory nerve transection on cell populations within the olfactory epithelium; and 4) ultrastructural investigations of reversible degeneration of olfactery receptors caused by elevated copper concentrations. The trout lofactory epithelium contains five cell types: ciliated epithelial cells, ciliated olfactory receptor cells, microvillar olfactory receptor cells, supporting cells, and basal cells. The ciliated and microvillar olfactory receptor cells and a small number of basal cells are backfilled by HRP when the tracer is applied to the cut olfactory nerve. When the olfactory nerve is cut, both ciliated and microvillar olfactory receptor cells degenerate within 2 days and are morphologically intact again within 8 days. When wild trout are taken from their native stream and placed in tanks with elevated copper concentrations, ciliated and microvillar cells degenerate. Replacement of these trout into their stream of origin is followed by morphologic restoration of both types of olfactory receptor cells. Ciliated and microvillar receptor cells are primary sensory bipolar neurons whose dendrites make contact with the environment; their axons travel directly to the brain. Consequently, substances can be transported directly from the environment into the brain via these “naked neurons.” Since fish cannot escape from the water in which they swim, and since that water may occasionally contain brain-toxic substances, the ability to close off - and later reopen - this anatomic gateway to the brain would confer a tremendous selective advantage upon animals that evolved the “brain-sparing” capacity to do so. Consequently, the unique regenerative powers of vertebrate olfactory receptor neurons may have their evolutionary origin in fishes. © 1992 Wiley-Liss, Inc.
1059-910X
1059910X
Wiley-Blackwell
shingle_catch_all_4 Moran, David Taylor
Rowley, J. Carter
Aiken, George R.
Jafek, Bruce W.
Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
Nose
Olfaction
Ultrastructure
Toxicology
Smell
Sensory
Fish
Life and Medical Sciences
Cell & Developmental Biology
This paper describes four investigations of the olfactory mucosa of the brown trout: 1) the ultrastructure of the olfactory mucosa as revealed by scanning (SEM), conventional transmission (TEM), and high voltage (HVEM) electron microscopy; 2) light and electron-microscopic investigations of retrograde transport of the tracer macromolecule horseradish peroxidase (HRP) when applied to the cut olfactory nerve; 3) SEM and TEM investigations of the effects of olfactory nerve transection on cell populations within the olfactory epithelium; and 4) ultrastructural investigations of reversible degeneration of olfactery receptors caused by elevated copper concentrations. The trout lofactory epithelium contains five cell types: ciliated epithelial cells, ciliated olfactory receptor cells, microvillar olfactory receptor cells, supporting cells, and basal cells. The ciliated and microvillar olfactory receptor cells and a small number of basal cells are backfilled by HRP when the tracer is applied to the cut olfactory nerve. When the olfactory nerve is cut, both ciliated and microvillar olfactory receptor cells degenerate within 2 days and are morphologically intact again within 8 days. When wild trout are taken from their native stream and placed in tanks with elevated copper concentrations, ciliated and microvillar cells degenerate. Replacement of these trout into their stream of origin is followed by morphologic restoration of both types of olfactory receptor cells. Ciliated and microvillar receptor cells are primary sensory bipolar neurons whose dendrites make contact with the environment; their axons travel directly to the brain. Consequently, substances can be transported directly from the environment into the brain via these “naked neurons.” Since fish cannot escape from the water in which they swim, and since that water may occasionally contain brain-toxic substances, the ability to close off - and later reopen - this anatomic gateway to the brain would confer a tremendous selective advantage upon animals that evolved the “brain-sparing” capacity to do so. Consequently, the unique regenerative powers of vertebrate olfactory receptor neurons may have their evolutionary origin in fishes. © 1992 Wiley-Liss, Inc.
1059-910X
1059910X
Wiley-Blackwell
shingle_title_1 Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
shingle_title_2 Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
shingle_title_3 Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
shingle_title_4 Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
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wilbert
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source_archive Wiley InterScience Backfile Collection 1832-2000
timestamp 2024-05-06T10:13:22.015Z
titel Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
titel_suche Ultrastructural neurobiology of the olfactory mucosa of the brown trout, Salmo trutta
topic TA-TD
uid nat_lic_papers_NLM160586356