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Electrogenetic cellular insulin release for real-time glycemic control in type 1 diabetic mice

Science. 2020 May 29;368(6494):993-1001. doi: 10.1126/science.aau7187.

Abstract

Sophisticated devices for remote-controlled medical interventions require an electrogenetic interface that uses digital electronic input to directly program cellular behavior. We present a cofactor-free bioelectronic interface that directly links wireless-powered electrical stimulation of human cells to either synthetic promoter-driven transgene expression or rapid secretion of constitutively expressed protein therapeutics from vesicular stores. Electrogenetic control was achieved by coupling ectopic expression of the L-type voltage-gated channel CaV1.2 and the inwardly rectifying potassium channel Kir2.1 to the desired output through endogenous calcium signaling. Focusing on type 1 diabetes, we engineered electrosensitive human β cells (Electroβ cells). Wireless electrical stimulation of Electroβ cells inside a custom-built bioelectronic device provided real-time control of vesicular insulin release; insulin levels peaked within 10 minutes. When subcutaneously implanted, this electrotriggered vesicular release system restored normoglycemia in type 1 diabetic mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bionics
  • Calcium Channels, L-Type / genetics
  • Calcium Signaling
  • Cell Engineering
  • Diabetes Mellitus, Experimental / therapy*
  • Diabetes Mellitus, Type 1 / therapy*
  • Electric Stimulation / instrumentation*
  • HEK293 Cells
  • Humans
  • Insulin Secretion / genetics*
  • Insulin-Secreting Cells / metabolism*
  • Male
  • Mice
  • Potassium Channels, Inwardly Rectifying / genetics
  • Prostheses and Implants
  • Transcription, Genetic
  • Transgenes
  • Wireless Technology / instrumentation*

Substances

  • Calcium Channels, L-Type
  • Kir2.1 channel
  • L-type calcium channel alpha(1C)
  • Potassium Channels, Inwardly Rectifying