4.8 Article

Synthetic beta cells for fusion-mediated dynamic insulin secretion

Journal

NATURE CHEMICAL BIOLOGY
Volume 14, Issue 1, Pages 86-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NCHEMBIO.2511

Keywords

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Funding

  1. American Diabetes Association [1-15-ACE-21]
  2. Alfred P. Sloan Foundation (Sloan Research Fellowship)
  3. National Science Foundation [1708620, 1542015]
  4. NC TraCS, NIH's Clinical and Translational Science Award (CTSA) at UNC-CH [1UL1TR001111]
  5. State of North Carolina
  6. NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES [UL1TR001111] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [F30DK113728] Funding Source: NIH RePORTER

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Generating artificial pancreatic beta cells by using synthetic materials to mimic glucose-responsive insulin secretion in a robust manner holds promise for improving clinical outcomes in people with diabetes. Here, we describe the construction of artificial beta cells (A beta Cs) with a multicompartmental 'vesicles-in-vesicle' superstructure equipped with a glucose-metabolism system and membrane-fusion machinery. Through a sequential cascade of glucose uptake, enzymatic oxidation and proton efflux, the A beta Cs can effectively distinguish between high and normal glucose levels. Under hyperglycemic conditions, high glucose uptake and oxidation generate a low pH (<5.6), which then induces steric deshielding of peptides tethered to the insulin-loaded inner small liposomal vesicles. The peptides on the small vesicles then form coiled coils with the complementary peptides anchored on the inner surfaces of large vesicles, thus bringing the membranes of the inner and outer vesicles together and triggering their fusion and insulin 'exocytosis'.

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