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Dynamic clustering of L-ˇ‐type Ca2+ -ˇ‐channels enables fast synchronized insulin secretion through localized Ca2+  nanodomains
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinsk cellbiologi.
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(Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
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Hälsovetenskaper
Identifikatorer
URN: urn:nbn:se:uu:diva-259062OAI: oai:DiVA.org:uu-259062DiVA, id: diva2:843067
Tillgänglig från: 2015-07-25 Skapad: 2015-07-25 Senast uppdaterad: 2015-10-01Bibliografiskt granskad
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1. Molecular mechanisms of biphasic insulin secretion
Öppna denna publikation i ny flik eller fönster >>Molecular mechanisms of biphasic insulin secretion
2015 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Pancreatic beta-cells secrete insulin in response to increase in blood glucose concentration with a rapid first phase and slower, sustained second phase. This secretion pattern is similar in entire pancreas, isolated islets of Langerhans and single beta-cells and it is disrupted in type 2-diabetes. Insulin stored in secretory vesicles has to undergo preparatory steps upon translocation to the plasma membrane which include docking and priming before being released by exocytosis. A better understanding of the molecules involved in these steps is required to determine the rate limiting factors for sustained secretion. Here these processes were studied in real time using total internal reflection fluorescence microscopy, which enables observation of insulin granules localized at the plasma membrane. A pool of granules morphologically docked at the plasma membrane was found to be depleted upon repeated stimulations. Recovery of the docked pool of granules took tens of minutes and became rate limiting for sustained secretion. Shorter depolarization stimuli did not deplete the docked pool and allowed rapid recovery of releasable granules. When a new granule arrived at the plasma membrane, docking was initiated by de novo formation of syntaxin/munc18 clusters at the docking site. Two-thirds of the granules which arrived at the plasma membrane failed to recruit these proteins and hence failed to dock. Priming involved recruitment of several other proteins including munc13, SNAP25 and Cav1.2 channels. Exocytosing granules were in close proximity to Ca2+ influx sites with high degree of association with Cav1.2 channels. This is because of the association of these channels to exocytosis site through syntaxin and SNAP25. During exocytosis the assembled release machinery disintegrated and the proteins at the release site dispersed. Syntaxin dispersal was initiated already during fusion pore formation rather than after release during exocytosis. This was studied using a newly developed red fluorescent probe - NPY-tdmOrange2 which was the most reliable pH sensitive red granule marker to label insulin granules. Overall these data give new insights into the molecular mechanisms involved in biphasic insulin secretion. Disturbances in the secretion at the level of granule docking and fusion may contribute to the early manifestations of type-2 diabetes.

Ort, förlag, år, upplaga, sidor
Uppsala: Acta Universitatis Upsaliensis, 2015. s. 42
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 1118
Nyckelord
Exocytosis, Insulin secretion, Membrane trafficking, Microscopy, Diabetes
Nationell ämneskategori
Medicin och hälsovetenskap
Forskningsämne
Medicinsk cellbiologi
Identifikatorer
urn:nbn:se:uu:diva-259071 (URN)978-91-554-9281-6 (ISBN)
Disputation
2015-09-11, B41, BMC, Husargatan 3, Uppsala, 09:15 (Engelska)
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Handledare
Tillgänglig från: 2015-08-21 Skapad: 2015-07-26 Senast uppdaterad: 2015-10-01

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Gandasi R., Nikhil

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