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The role of neurotrophins in regulating spiral ganglion morphology

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TitleInfo
Title
The role of neurotrophins in regulating spiral ganglion morphology
Name (type = personal)
NamePart (type = family)
Smith
NamePart (type = given)
Felicia L.
NamePart (type = date)
1982-
DisplayForm
Felicia L. Smith
Role
RoleTerm (authority = RULIB)
author
Name (type = personal)
NamePart (type = family)
Davis
NamePart (type = given)
Robin L
DisplayForm
Robin L Davis
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
chair
Name (type = personal)
NamePart (type = family)
Plummer
NamePart (type = given)
Mark
DisplayForm
Mark Plummer
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = personal)
NamePart (type = family)
Hsu
NamePart (type = given)
Shu-Chan
DisplayForm
Shu-Chan Hsu
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = personal)
NamePart (type = family)
Dreyfus
NamePart (type = given)
Cheryl
DisplayForm
Cheryl Dreyfus
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = personal)
NamePart (type = family)
Olson
NamePart (type = given)
Elizabeth
DisplayForm
Elizabeth Olson
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
outside member
Name (type = corporate)
NamePart
Rutgers University
Role
RoleTerm (authority = RULIB)
degree grantor
Name (type = corporate)
NamePart
Graduate School - New Brunswick
Role
RoleTerm (authority = RULIB)
school
TypeOfResource
Text
Genre (authority = marcgt)
theses
OriginInfo
DateCreated (qualifier = exact)
2014
DateOther (qualifier = exact); (type = degree)
2014-10
Place
PlaceTerm (type = code)
xx
CopyrightDate (encoding = w3cdtf)
2014
Language
LanguageTerm (authority = ISO639-2b); (type = code)
eng
Abstract (type = abstract)
Many structural features of spiral ganglion neurons are specifically designed to carry out frequency-specific coding. Specific morphological properties correspond to tonotopic position along the cochlea contour, which include soma area and axon length. To examine how these features are regulated, we used various preparations. Thus, soma area is altered in a predictable manner corresponding to the frequency location of its peripheral target tissue. The sensory endorgan alters the axon characteristics of the spiral ganglion neurons. The regenerated axons have peripheral nervous system-like (PNS) and central nervous system-like (CNS) axon profiles that enable the examination of putative PNS/CNS axon length ratios. Similar to their in vivo patterns, the putative peripheral axons regenerated from low frequency neurons extend their processes a longer distance than high frequency neurons. This pattern is altered when the neuronal explants are paired with peripheral target tissue isolated from different cochlear regions. To identify the regulatory factors that control these structural features, we investigated brain derived neurotrophic factor (BDNF) and neurotrophin 3 (NT3). These neurotrophins control the ion channel composition that mediates the neuronal firing patterns (Adamson et al., 2002) and the synaptic protein levels (Flores-Otero et al., 2007) in spiral ganglion neurons. For example, the exposure to BDNF transformed neurons isolated from the apical or basal region phenotypic properties to resemble basal neurons. In contrast, the exposure to NT3 transformed the phenotypic properties of both apical and basal neurons to resemble apical neurons. We investigated whether soma area and axon length conforms to the same regulatory mechanism. In the neuronal explant cultures, exposure to BDNF or NT3 had limited or no influence on cell size. Moreover, the effect of the peripheral target tissue on axon length is modulated by BDNF and NT3. However, both neurotrophins have a differential result on the axon length of spiral ganglion neurons isolated from distinct cochlear regions. In all, frequency specific signals within the organ of Corti direct the structural phenotype of spiral ganglion neurons. These results indicate a different regulatory mechanism is needed to alter the structural phenotype within the spiral ganglion.
Subject (authority = RUETD)
Topic
Neuroscience
Subject (authority = ETD-LCSH)
Topic
Neurotrophic functions
Subject (authority = ETD-LCSH)
Topic
Neurons--Physiology
RelatedItem (type = host)
TitleInfo
Title
Rutgers University Electronic Theses and Dissertations
Identifier (type = RULIB)
ETD
Identifier
ETD_5930
PhysicalDescription
Form (authority = gmd)
electronic resource
InternetMediaType
application/pdf
InternetMediaType
text/xml
Extent
1 online resource (viii, 117 p. : ill.)
Note (type = degree)
Ph.D.
Note (type = bibliography)
Includes bibliographical references
Note (type = statement of responsibility)
by Felicia L. Smith
RelatedItem (type = host)
TitleInfo
Title
Graduate School - New Brunswick Electronic Theses and Dissertations
Identifier (type = local)
rucore19991600001
Location
PhysicalLocation (authority = marcorg); (displayLabel = Rutgers, The State University of New Jersey)
NjNbRU
Identifier (type = doi)
doi:10.7282/T31V5GKB
Genre (authority = ExL-Esploro)
ETD doctoral
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Rights

RightsDeclaration (ID = rulibRdec0006)
The author owns the copyright to this work.
RightsHolder (type = personal)
Name
FamilyName
Smith
GivenName
Felicia
MiddleName
L.
Role
Copyright Holder
RightsEvent
Type
Permission or license
DateTime (encoding = w3cdtf); (qualifier = exact); (point = start)
2014-09-30 12:58:27
AssociatedEntity
Name
Felicia Smith
Role
Copyright holder
Affiliation
Rutgers University. Graduate School - New Brunswick
AssociatedObject
Type
License
Name
Author Agreement License
Detail
I hereby grant to the Rutgers University Libraries and to my school the non-exclusive right to archive, reproduce and distribute my thesis or dissertation, in whole or in part, and/or my abstract, in whole or in part, in and from an electronic format, subject to the release date subsequently stipulated in this submittal form and approved by my school. I represent and stipulate that the thesis or dissertation and its abstract are my original work, that they do not infringe or violate any rights of others, and that I make these grants as the sole owner of the rights to my thesis or dissertation and its abstract. I represent that I have obtained written permissions, when necessary, from the owner(s) of each third party copyrighted matter to be included in my thesis or dissertation and will supply copies of such upon request by my school. I acknowledge that RU ETD and my school will not distribute my thesis or dissertation or its abstract if, in their reasonable judgment, they believe all such rights have not been secured. I acknowledge that I retain ownership rights to the copyright of my work. I also retain the right to use all or part of this thesis or dissertation in future works, such as articles or books.
Copyright
Status
Copyright protected
Availability
Status
Open
Reason
Permission or license
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RULTechMD (ID = TECHNICAL1)
ContentModel
ETD
OperatingSystem (VERSION = 5.1)
windows xp
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