4.8 Article

Smartphone-Flashlight-Mediated Remote Control of Rapid Insulin Secretion Restores Glucose Homeostasis in Experimental Type-1 Diabetes

Journal

SMALL
Volume 17, Issue 35, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202101939

Keywords

cell-based therapies; optogenetics; smartphone; synthetic biology; type-1 diabetes

Funding

  1. European Research Council [785800]
  2. National Center of Competence in Research (NCCR) for Molecular Systems Engineering
  3. EC [964497]

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The study demonstrates the successful utilization of smartphone-induced insulin release technology, allowing for repeated and reversible insulin secretion within 15 minutes in response to light stimulation, with a high induction fold both in vitro and in vivo. The programmable percutaneous remote control of implanted microencapsulated i beta-cells with a smartphone's flashlight rapidly reverses hyperglycemia in a mouse model of type-1 diabetes.
Emerging digital assessment of biomarkers by linking health-related data obtained from wearable electronic devices and embedded health and fitness sensors in smartphones is opening up the possibility of creating a continuous remote-monitoring platform for disease management. It is considered that the built-in flashlight of smartphones may be utilized to remotely program genetically engineered designer cells for on-demand delivery of protein-based therapeutics. Here, the authors present smartphone-induced insulin release in beta-cell line (i beta-cell) technology for traceless light-triggered rapid insulin secretion, employing the light-activatable receptor melanopsin to induce calcium influx and membrane depolarization upon illumination. This i beta-cell-based system enables repeated, reversible secretion of insulin within 15 min in response to light stimulation, with a high induction fold both in vitro and in vivo. It is shown that programmable percutaneous remote control of implanted microencapsulated i beta-cells with a smartphone's flashlight rapidly reverses hyperglycemia in a mouse model of type-1 diabetes.

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