Smartphone-controlled optogenetically engineered cells enable semiautomatic glucose homeostasis in diabetic mice

  • Jiawei Shao
  • , Shuai Xue
  • , Guiling Yu
  • , Yuanhuan Yu
  • , Xueping Yang
  • , Yu Bai
  • , Sucheng Zhu
  • , Linfeng Yang
  • , Jianli Yin
  • , Yidan Wang
  • , Shuyong Liao
  • , Sanwei Guo
  • , Mingqi Xie
  • , Martin Fussenegger
  • , Haifeng Ye*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

188 Scopus citations

Abstract

With the increasingly dominant role of smartphones in our lives, mobile health care systems integrating advanced point-of-care technologies to manage chronic diseases are gaining attention. Using a multidisciplinary design principle coupling electrical engineering, software development, and synthetic biology, we have engineered a technological infrastructure enabling the smartphone-Assisted semiautomatic treatment of diabetes in mice. A custom-designed home server SmartController was programmed to process wireless signals, enabling a smartphone to regulate hormone production by optically engineered cells implanted in diabetic mice via a farred light (FRL)-responsive optogenetic interface. To develop this wireless controller network, we designed and implanted hydrogel capsules carrying both engineered cells and wirelessly powered FRL LEDs (light-emitting diodes). In vivo production of a short variant of human glucagon-like peptide 1 (shGLP-1) or mouse insulin by the engineered cells in the hydrogel could be remotely controlled by smartphone programs or a custom-engineered Bluetooth-Active glucometer in a semiautomatic, glucose-dependent manner. By combining electronic device- generated digital signals with optogenetically engineered cells, this study provides a step toward translating cellbased therapies into the clinic.

Original languageEnglish
Article number2298
JournalScience Translational Medicine
Volume9
Issue number387
DOIs
StatePublished - 26 Apr 2017

Fingerprint

Dive into the research topics of 'Smartphone-controlled optogenetically engineered cells enable semiautomatic glucose homeostasis in diabetic mice'. Together they form a unique fingerprint.

Cite this