Knockout of syntaxin-4 in 3T3-L1 adipocytes reveals new insight into GLUT4 trafficking and adiponectin secretion
Black, Hannah L. and Livingstone, Rachel and Mastick, Cynthia C. and Al Tobi, Mohammed and Taylor, Holly and Geiser, Angéline and Stirrat, Laura and Kioumourtzoglou, Dimitrios and Petrie, John R. and Boyle, James G. and Bryant, Nia J. and Gould, Gwyn W. (2022) Knockout of syntaxin-4 in 3T3-L1 adipocytes reveals new insight into GLUT4 trafficking and adiponectin secretion. Journal of Cell Science, 135 (1). 258375. ISSN 0021-9533 (https://doi.org/10.1242/jcs.258375)
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Abstract
Adipocytes are key to metabolic regulation, exhibiting insulin-stimulated glucose transport that is underpinned by the insulin-stimulated delivery of glucose transporter type 4 (SLC2A4, also known and hereafter referred to as GLUT4)-containing vesicles to the plasma membrane where they dock and fuse, and increase cell surface GLUT4 levels. Adipocytokines, such as adiponectin, are secreted via a similar mechanism. We used genome editing to knock out syntaxin-4, a protein reported to mediate fusion between GLUT4-containing vesicles and the plasma membrane in 3T3-L1 adipocytes. Syntaxin-4 knockout reduced insulin-stimulated glucose transport and adiponectin secretion by ∼50% and reduced GLUT4 levels. Ectopic expression of haemagglutinin (HA)-tagged GLUT4 conjugated to GFP showed that syntaxin-4-knockout cells retain significant GLUT4 translocation capacity, demonstrating that syntaxin-4 is dispensable for insulin-stimulated GLUT4 translocation. Analysis of recycling kinetics revealed only a modest reduction in the exocytic rate of GLUT4 in knockout cells, and little effect on endocytosis. These analyses demonstrate that syntaxin-4 is not always rate limiting for GLUT4 delivery to the cell surface. In sum, we show that syntaxin-4 knockout results in reduced insulin-stimulated glucose transport, depletion of cellular GLUT4 levels and inhibition of adiponectin secretion but has only modest effects on the translocation capacity of the cells.
ORCID iDs
Black, Hannah L., Livingstone, Rachel, Mastick, Cynthia C., Al Tobi, Mohammed, Taylor, Holly, Geiser, Angéline ORCID: https://orcid.org/0000-0002-7108-2440, Stirrat, Laura, Kioumourtzoglou, Dimitrios, Petrie, John R., Boyle, James G., Bryant, Nia J. and Gould, Gwyn W. ORCID: https://orcid.org/0000-0001-6571-2875;-
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Item type: Article ID code: 78909 Dates: DateEvent10 January 2022Published3 December 2021Published Online18 November 2021AcceptedSubjects: Science > Microbiology
Medicine > Therapeutics. PharmacologyDepartment: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 15 Dec 2021 12:26 Last modified: 11 Nov 2024 13:19 URI: https://strathprints.strath.ac.uk/id/eprint/78909