Abstract
dc:description.abstract<p>Calcium (Ca<sup>2+</sup>) plays an important role as a second messenger, transmitting the message of arrival of stimuli such as hormones and neurotransmitters to the intracellular system that carries out the cellular response to the stimulus. The universality of Ca<sup>2+</sup> as an intracellular messenger depends on its enormous versatility. This versatility is exploited to control processes as diverse as fertilization, proliferation, development, learning and memory, contraction and secretion, and must be accomplished within the context of Ca<sup>2+</sup> being highly toxic.</p><p>Ryanodine receptors (RyRs) and inositol trisphosphate receptors (IP<sub>3</sub>Rs) are Ca<sup>2+</sup> -release channels located on intracellular membranes of the endoplasmic reticulum (ER)/sarcoplasmic reticulum (SR) that perform essential functions as key targets of hormone/neurotransmitter action to initiate intracellular Ca<sup>2+</sup> signals. The purpose of this project was to study the role of RyR<sub>2</sub> in Ca<sup>2+</sup> signaling in the NG115-401L neuronal cell line. siRNA transfection methods were employed to knockdown RyR<sub>2</sub> expression levels in NG115-401L cells. We used reverse transcription and real-time PCR to evaluate RyR2 gene expression in transfected/untransfected cells. We also evaluated cytosolic Ca<sup>2+</sup> changes induced by RyR activators or regulators, using fura-2 AM as the Ca<sup>2+</sup> indicator. Successful RyR<sub>2</sub> gene knockdown allowed us to carry out some initial experiments to characterize the specific roles played by the RyR<sub>2</sub> receptor isoform. We examined cell responses to FK-506 under the condition of RyR<sub>2</sub> knockdown, finding that RyR<sub>2</sub> appears to confer selectivity to this response. Finally, the effects of siRNA transfection and FK-506 treatment on NG115-401L cell growth were evaluated. These experimental results may contribute to future studies of RyR<sub>2</sub>, and help develop novel treatments for RyR<sub>2</sub>-base d dysfunctional diseases.</p>
Degree
thesis:*- Name thesis:degree_name
- Master of Science (M.S.)
- Level thesis:degree_level
- Thesis - Pacific Access Restricted
- Discipline thesis:degree_discipline
- Pharmaceutical and Chemical Sciences
- Year dc:date.available
- 2008
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Li, Yiming
- Contributors dc:contributor
-
- David Thomas
Subjects
dc:subject × 7Rights
dc:rightsIdentifiers
dc:identifier.*- Repository record dc:identifier
- https://scholarlycommons.pacific.edu/uop_etds/710
- OAI identifier oai:identifier
- oai:scholarlycommons.pacific.edu:uop_etds-1709