Title Information
Title
Diverse subtypes of fast-spiking inhibitory neurons in neocortex
Name: Personal
Name Part
Sugden, Arthur U
Role
Role Term: Text
creator
Origin Information
Copyright Date
2015
Physical Description
Extent
xx, 132 p.
digitalOrigin
born digital
Note
Thesis (Ph.D. -- Brown University (2015)
Name: Personal
Name Part
Connors, Barry
Role
Role Term: Text
Director
Name: Personal
Name Part
Cruikshank, Scott
Role
Role Term: Text
Director
Name: Personal
Name Part
Barnea, Gilad
Role
Role Term: Text
Reader
Name: Personal
Name Part
Berson, David
Role
Role Term: Text
Reader
Name: Personal
Name Part
Jaworski, Alexander
Role
Role Term: Text
Reader
Name: Personal
Name Part
Harwell, Corey
Role
Role Term: Text
Reader
Name: Corporate
Name Part
Brown University. BIOMED: Molecular Biology, Cell Biology, and Biochemistry
Role
Role Term: Text
sponsor
Genre (aat)
theses
Abstract
Inhibitory interneurons are essential for normal cortical function. They prevent seizures, regulate temporal and spatial coding, and generate oscillations and synchrony in pyramidal cells. The largest subtype of inhibitory interneurons is fast-spiking (FS) cells, which mediate feedforward inhibition and have been implicated in the generation of gamma oscillations, the oscillations that may bind a percept together as it passes through groups of neurons. FS cells are canonically marked by the calcium-binding protein parvalbumin (PV), whose levels have been linked to synaptic plasticity. Like-types of adult neocortical inhibitory neurons are linked by gap junctions with a probability of greater than 50\% within 50 microns. FS cells are linked by gap junctions, and these gap junctions have long been thought to add to the generation of gamma oscillations. In this dissertation I have asked two questions. First, ventral postrhinal cortex, a subset of the parahippocampal region, lacks canonical PV-expressing FS cells. Within this area, it has been possible to ask how is inhibition altered in a neocortical region lacking canonical FS cells? Second, using a two-pronged approach of in vitro electrophysiology and a computational model, I have asked what roles do gap junctions play in neocortical gamma oscillations? In examining these problems, I have found three results. First, the commonly-stated overlap between parvalbumin (PV) and FS cells does not apply in ventral postrhinal cortex. The majority of FS cells in this region are PV-negative, and these cells extend into neighboring cortex with canonical FS cells. Second, the absence of canonical FS cells from vPOR and the corresponding decrease in inhibitory cell density does not decrease total inhibition onto excitatory cells, due to decreased inhibition onto inhibitory cells in vPOR. Third, gamma oscillations do not require gap junctions in neocortex, unless compensation in RS cells for the lack of gap junctions in inhibitory cells is masking the effect.
Subject
Topic
inhibitory
Subject
Topic
gamma
Subject
Topic
parvalbumin
Subject
Topic
fast-spiking
Record Information
Record Content Source (marcorg)
RPB
Record Creation Date (encoding="iso8601")
20150601
Language
Language Term: Code (ISO639-2B)
eng
Language Term: Text
English
Identifier: DOI
10.7301/Z0QC01WF
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In Copyright
Access Condition: restriction on access
Collection is open for research.
Type of Resource (primo)
dissertations