A 4D view on insulin secretory granule turnover in the β‐cell. (September 2017)

• Record Type: Journal Article
• Authors: Müller, Andreas; Mziaut, Hassan; Neukam, Martin; Knoch, Klaus‐Peter; Solimena, Michele
• Other Names: Cerasi Erol guestEditor.; Accili Domenico guestEditor.; Ahrén Bo guestEditor.; Boitard Christian guestEditor.; Seino Susumu guestEditor.; Thorens Bernard guestEditor.
• Is Part Of: Diabetes, obesity & metabolism. Volume 19(2017)Supplement 1
• Page Start: 107
• Page End: 114
• Publication Date: 2017-09
• Subjects: insulin degradation -- insulin secretion -- insulin secretory granule ageing -- microscopy -- SNAP tag; Diabetes -- Periodicals; Obesity -- Periodicals; Metabolism -- Disorders -- Periodicals; Clinical pharmacology -- Periodicals; 616.462
• DOI: 10.1111/dom.13015
• Languages: English
• ISSNs: 1462-8902

Abstract

Abstract : Insulin secretory granule (SG) turnover consists of several highly regulated processes allowing for proper β‐cell function and insulin secretion. Besides the spatial distribution of insulin SGs, their age has great impact on the likelihood of their secretion and their behaviour within the β‐cell. While quantitative measurements performed decades ago demonstrated the preferential secretion of young insulin, new experimental approaches aim to investigate insulin ageing at the granular level. Live‐cell imaging, automated image analysis and correlative light and electron microscopy have fostered knowledge of age‐defined insulin SG dynamics, their interaction with the cytoskeleton and ultrastructural features. Here, we review our recent work in regards to the connection between insulin SG age, SG dynamics, intracellular location and interaction with other proteins.