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dc.contributor.authorLevy, Elana
dc.date.accessioned2018-11-05T21:11:05Z
dc.date.available2018-11-05T21:11:05Z
dc.date.issued2015-04
dc.identifier.urihttps://hdl.handle.net/20.500.12202/4069
dc.identifier.urihttps://yulib002.mc.yu.edu/login?url=https://repository.yu.edu/handle/20.500.12202/4069
dc.descriptionThe file is restricted for YU community access only.
dc.description.abstractIn humans, insulin release is necessary to the regulation of the metabolism and is triggered by the presence of glucose in the bloodstream. Insulin release originates from beta cells of the islets of Langerhans in the pancreas, where it is stored in approximately 10,000 secretory granules per cell12 . Its release is triggered by the presence of excess glucose in the blood, which would be toxic if not processed promptly. A loss of insulin content or mechanistic control of insulin release can result in various metabolic conditions including, classically, diabetes mellitus3 . After stimulation and synthesis, insulin must be packaged into granules for exocytotic release. These secretory granules are instrumental for the efficient and effective release of insulin into the bloodstream. Secretagogue stimulation results in the transcription, translation, and release of insulin through these transport vesicles. This secretory regulation is critical in ensuring proper control over diverse signaling events, including cell metabolism, growth, and differentiation4 . While long-studied, no formal consensus exists regarding the precise mechanisms responsible for packaging of insulin into granules, how these loaded granules are transported to the cell surface, and then their release of contents into the bloodstream during periods of prolonged cell stimulation56 . Particularly in the case of insulin secretion, to date, the exact mechanisms remain poorly characterized and controversial. The central question revolves around the kinetics of insulin granule recruitment and release upon reaching the release zone.en_US
dc.language.isoen_USen_US
dc.publisherStern College for Womenen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectInsulin --Mechanism of action --Research.en_US
dc.subjectGlucose --Mechanism of action --Research.en_US
dc.subjectCryomicroscopy.en_US
dc.subjectCytoplasmic granules --Research.en_US
dc.subjectGranular flow --Research.en_US
dc.titleQuantitation of Secretory Granule Dynamics During Glucose Stimulationen_US
dc.typeThesisen_US


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  • Honors Student Theses [208]
    Senior honors theses sponsored by the S. Daniel Abraham Honors Program of Stern College for Women

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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States