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A dual-transduction-integrated biosensing system to examine the 3D cell-culture for bone regeneration

  • Evgeny Kozhevnikov
  • , Shupei Qiao
  • , Fengtong Han
  • , Wei Yan
  • , Yufang Zhao
  • , Xiaolu Hou
  • , Alaka Acharya
  • , Yijun Shen
  • , Hui Tian
  • , Haijiao Zhang
  • , Xiongbiao Chen
  • , Yuanchuan Zheng
  • , Hongji Yan
  • , Mian Guo
  • , Weiming Tian*
  • *Corresponding author for this work
  • School of Life Science and Technology, Harbin Institute of Technology
  • The First Affiliated Hospital of Harbin Medical University
  • University of Saskatchewan
  • School of Chemistry and Chemical Engineering, Harbin Institute of Technology
  • KTH Royal Institute of Technology
  • The Second Affiliated Hospital of Harbin Medical University

Research output: Contribution to journalArticlepeer-review

Abstract

Three-dimensional (3D) cell cultures developed with living cells and scaffolds have demonstrated outstanding potential for tissue engineering and regenerative medicine applications. However, no suitable tools are available to monitor dynamically variable cell behavior in such a complex microenvironment. In particular, simultaneously assessing cell behavior, cell secretion, and the general state of a 3D culture system is of a really challenging task. This paper presents our development of a dual-transduction-integrated biosensing system that assesses electrical impedance in conjunction with imaging techniques to simultaneously investigate the 3D cell-culture for bone regeneration. First, we created models to mimic the dynamic deposition of the extracellular matrix (ECM) in 3D culture, which underwent osteogenesis by incorporating different amounts of bone–ECM components (collagen, hydroxyapatite [HAp], and hyaluronic acid [HA]) into alginate-based hydrogels. The formed models were investigated by means of electrical impedance spectroscopy (EIS), with the results showing that the impedances increased linearly with collagen and hyaluronan, but changed in a more complex manner with HAp. Thereafter, we created two models that consisted of primary osteoblast cells (OBs), which expressed the enhanced green fluorescent protein (EGFP), and 4T1 cells, which secreted the EGFP-HA, in the alginate hydrogel. We found the capacitance (associated with impedance and measured by EIS) increased with the increases in initial embedded OBs, and also confirmed the cell proliferation over 3 days with the EGFP signal as monitored by the fluorescent imaging component in our system. Interestingly, the change in capacitance is found to be associated with OB migration following stimulation. Also, we show higher capacitance in 4T1 cells that secret HA when compared to control 4T1 cells after a 3-day culture. Taken together, we demonstrate that our biosensing system is able to investigate the dynamic process of 3D culture in a non-invasive and real-time manner.

Original languageEnglish
Article number111481
JournalBiosensors and Bioelectronics
Volume141
DOIs
StatePublished - 15 Sep 2019
Externally publishedYes

Keywords

  • Bone regeneration
  • Electrical impedance
  • Fluorescence imaging

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