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dc.contributor.authorFonseca, Sonya G.
dc.contributor.authorGromada, Jesper
dc.contributor.authorUrano, Fumihiko
dc.date2022-08-11T08:10:15.000
dc.date.accessioned2022-08-23T17:01:09Z
dc.date.available2022-08-23T17:01:09Z
dc.date.issued2011-07-05
dc.date.submitted2011-08-01
dc.identifier.citationTrends Endocrinol Metab. 2011 Jul;22(7):266-74. Epub 2011 Mar 31. <a href="http://dx.doi.org/10.1016/j.tem.2011.02.008">Link to article on publisher's site</a>
dc.identifier.issn1043-2760 (Linking)
dc.identifier.doi10.1016/j.tem.2011.02.008
dc.identifier.pmid21458293
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43944
dc.description.abstractIn pancreatic beta-cells, the endoplasmic reticulum (ER) is an important cellular compartment for insulin biosynthesis, which accounts for half of the total protein production in these cells. Protein flux through the ER must be carefully monitored to prevent dysregulation of ER homeostasis and stress. ER stress elicits a signaling cascade known as the unfolded protein response (UPR), which influences both life and death decisions in cells. beta-cell loss is a pathological component of both type 1 and type 2 diabetes, and recent findings suggest that ER stress is involved. In this review, we address the transition from the physiological ER stress response to the pathological response, and explore the mechanisms of ER stress-mediated beta-cell loss during the progression of diabetes.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=21458293&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.tem.2011.02.008
dc.subjectEndoplasmic Reticulum
dc.subjectUnfolded Protein Response
dc.subjectHomeostasis
dc.subjectDiabetes Mellitus
dc.subjectCell Death
dc.subjectStress, Physiological
dc.subjectGenetics and Genomics
dc.titleEndoplasmic reticulum stress and pancreatic beta-cell death
dc.typeJournal Article
dc.source.journaltitleTrends in endocrinology and metabolism: TEM
dc.source.volume22
dc.source.issue7
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pgfe_pp/155
dc.identifier.contextkey2124690
html.description.abstract<p>In pancreatic beta-cells, the endoplasmic reticulum (ER) is an important cellular compartment for insulin biosynthesis, which accounts for half of the total protein production in these cells. Protein flux through the ER must be carefully monitored to prevent dysregulation of ER homeostasis and stress. ER stress elicits a signaling cascade known as the unfolded protein response (UPR), which influences both life and death decisions in cells. beta-cell loss is a pathological component of both type 1 and type 2 diabetes, and recent findings suggest that ER stress is involved. In this review, we address the transition from the physiological ER stress response to the pathological response, and explore the mechanisms of ER stress-mediated beta-cell loss during the progression of diabetes.</p>
dc.identifier.submissionpathpgfe_pp/155
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentProgram in Gene Function and Expression
dc.source.pages266-74


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