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Three-dimensional mapping and regulation of action potential propagation in nanoelectronics-innervated tissues

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Abstract

Real-time mapping and manipulation of electrophysiology in three-dimensional (3D) tissues could have important impacts on fundamental scientific and clinical studies, yet realization is hampered by a lack of effective methods. Here we introduce tissue-scaffold-mimicking 3D nanoelectronic arrays consisting of 64 addressable devices with subcellular dimensions and a submillisecond temporal resolution. Real-time extracellular action potential (AP) recordings reveal quantitative maps of AP propagation in 3D cardiac tissues, enable in situ tracing of the evolving topology of 3D conducting pathways in developing cardiac tissues and probe the dynamics of AP conduction characteristics in a transient arrhythmia disease model and subsequent tissue self-adaptation. We further demonstrate simultaneous multisite stimulation and mapping to actively manipulate the frequency and direction of AP propagation. These results establish new methodologies for 3D spatiotemporal tissue recording and control, and demonstrate the potential to impact regenerative medicine, pharmacology and electronic therapeutics.

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Figure 1: 3D spatiotemporal mapping of APs.
Figure 2: AP evolution during tissue development.
Figure 3: Arrhythmia induced by localized norepinephrine injection.
Figure 4: Active spatiotemporal regulation of APs.

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Change history

  • 21 July 2016

    In the version of this Article originally published online, in Fig. 1e, the traces for devices (1,2) and (2,3) were incorrect. This has now been corrected in all versions of the Article. In addition, the original data for Fig. 1d (from which Fig. 1e was extracted) is now provided as Supplementary Data.

References

  1. Langer, R. & Vacanti, J. P. Tissue engineering. Science 260, 920–926 (1993).

    Article  CAS  Google Scholar 

  2. Eschenhagen, T. & Zimmermann, W. H. Engineering myocardial tissue. Circ. Res. 97, 1220–1231 (2005).

    Article  CAS  Google Scholar 

  3. Shimizu, T. et al. Fabrication of pulsatile cardiac tissue grafts using a novel 3-dimensional cell sheet manipulation technique and temperature-responsive cell culture surfaces. Circ. Res. 90, e40 (2002).

    Article  CAS  Google Scholar 

  4. Dvir, T., Timko, B. P., Kohane, D. S. & Langer, R. Nanotechnological strategies for engineering complex tissues. Nature Nanotech. 6, 13–22 (2011).

    Article  CAS  Google Scholar 

  5. Papadaki, M. et al. Tissue engineering of functional cardiac muscle: molecular, structural, and electrophysiological studies. Am. J. Physiol. Heart Circ. Physiol. 280, 168–178 (2001).

    Article  Google Scholar 

  6. Hansen, A. et al. Development of a drug screening platform based on engineered heart tissue. Circ. Res. 107, 35–44 (2010).

    Article  CAS  Google Scholar 

  7. Grosberg, A., Alford, P. W., McCain, M. L. & Parker, K. K. Ensembles of engineered cardiac tissues for physiological and pharmacological study: heart on a chip. Lab Chip 11, 4165–4173 (2011).

    Article  CAS  Google Scholar 

  8. Natarajan, A. et al. Patterned cardiomyocytes on microelectrode arrays as a functional, high information content drug screening platform. Biomaterials 32, 4267–4274 (2011).

    Article  CAS  Google Scholar 

  9. Griffith, L. G. & Naughton, G. Tissue engineering-current challenges and expanding opportunities. Science 295, 1009–1014 (2002).

    Article  CAS  Google Scholar 

  10. Furuta, A. et al. Pulsatile cardiac tissue grafts using a novel three-dimensional cell sheet manipulation technique functionally integrates with the host heart, in vivo. Circ. Res. 98, 705–712 (2006).

    Article  CAS  Google Scholar 

  11. Zimmermann, W. H. et al. Engineered heart tissue grafts improve systolic and diastolic function in infarcted rat hearts. Nature Med. 12, 452–458 (2006).

    Article  CAS  Google Scholar 

  12. St-Pierre, F. et al. High-fidelity optical reporting of neuronal electrical activity with an ultrafast fluorescent voltage sensor. Nature Neurosci. 17, 884–889 (2014).

    Article  CAS  Google Scholar 

  13. Herron, T. J., Lee, P. & Jalife, J. Optical imaging of voltage and calcium in cardiac cells & tissues. Circ. Res. 110, 609–623 (2012).

    Article  CAS  Google Scholar 

  14. Kralj, J. M., Douglass, A. D., Hochbaum, D. R., Maclaurin, D. & Cohen, A. E. Optical recording of action potentials in mammalian neurons using a microbial rhodopsin. Nat. Methods 9, 90–95 (2012).

    Article  CAS  Google Scholar 

  15. Huisken, J., Swoger, J., Del Bene, F., Wittbrodt, J. & Stelzer, E. H. K. Optical sectioning deep inside live embryos by selective plane illumination microscopy. Science 305, 1007–1009 (2004).

    Article  CAS  Google Scholar 

  16. Kim, D. H. et al. Materials for multifunctional balloon catheters with capabilities in cardiac electrophysiological mapping and ablation therapy. Nature Mater. 10, 316–323 (2011).

    Article  CAS  Google Scholar 

  17. Cohen-Karni, T., Timko, B. P., Weiss, L. E. & Lieber, C. M. Flexible electrical recording from cells using nanowire transistor arrays. Proc. Natl Acad. Sci. USA 106, 7309–7313 (2009).

    Article  CAS  Google Scholar 

  18. Viventi, J. et al. A conformal, bio-interfaced class of silicon electronics for mapping cardiac electrophysiology. Sci. Transl. Med. 2, 24ra22 (2010).

    Article  Google Scholar 

  19. Tian, B. Z. et al. Macroporous nanowire nanoelectronic scaffolds for synthetic tissues. Nature Mater. 11, 986–994 (2012).

    Article  CAS  Google Scholar 

  20. Place, E. S., George, J. H., Williams, C. K. & Stevens, M. M. Synthetic polymer scaffolds for tissue engineering. Chem. Soc. Rev. 38, 1139–1151 (2009).

    Article  CAS  Google Scholar 

  21. Zhang, D. et al. Tissue-engineered cardiac patch for advanced functional maturation of human ESC-derived cardiomyocytes. Biomaterials 34, 5813–5820 (2013).

    Article  CAS  Google Scholar 

  22. Yelbuz, T. M., Choma, M. A., Thrane, L., Kirby, M. L. & Izatt, J. A. Optical coherence tomography – a new high-resolution imaging technology to study cardiac development in chick embryos. Circulation 106, 2771–2774 (2002).

    Article  Google Scholar 

  23. Miragoli, M., Gaudesius, G. & Rohr, S. Electrotonic modulation of cardiac impulse conduction by myofibroblasts. Circ. Res. 98, 801–810 (2006).

    Article  CAS  Google Scholar 

  24. Khademhosseini, A. et al. Microfluidic patterning for fabrication of contractile cardiac organoids. Biomed. Microdev. 9, 149–157 (2007).

    Article  Google Scholar 

  25. Timko, B. P., Cohen-Karni, T., Qing, Q., Tian, B. & Lieber, C. M. Design and implementation of functional nanoelectronic interfaces with biomolecules, cells, and tissue using nanowire device arrays. IEEE Trans. Nanotechnol. 9, 269–280 (2010).

    Article  Google Scholar 

  26. Zhang, J. H. et al. Functional cardiomyocytes derived from human induced pluripotent stem cells. Circ. Res. 104, e30 (2009).

    CAS  Google Scholar 

  27. Laflamme, M. A. et al. Cardiomyocytes derived from human embryonic stem cells in pro-survival factors enhance function of infarcted rat hearts. Nature Biotechnol. 25, 1015–1024 (2007).

    Article  CAS  Google Scholar 

  28. Myles, R. C., Wang, L. G., Kang, C. Y., Bers, D. M. & Ripplinger, C. M. Local beta-adrenergic stimulation overcomes source-sink mismatch to generate focal arrhythmia. Circ. Res. 110, 1454–1464 (2012).

    Article  CAS  Google Scholar 

  29. Iravanian, S. et al. Functional reentry in cultured monolayers of neonatal rat cardiac cells. Am. J. Physiol. Heart Circ. Physiol. 285, 449–456 (2003).

    Article  Google Scholar 

  30. Liu, J. et al. Syringe-injectable electronics. Nature Nanotech. 10, 629–636 (2015).

    Article  CAS  Google Scholar 

  31. Garbern, J. C. & Lee, R. T. Cardiac stem cell therapy and the promise of heart regeneration. Cell Stem Cell 12, 689–698 (2013).

    Article  CAS  Google Scholar 

  32. Wobma, H. & Vunjak-Novakovic, G. Tissue engineering and regenerative medicine 2015: a year in review. Tissue Eng. Part B Rev. 22, 101–113 (2016).

    Article  Google Scholar 

  33. Wong, A. D. et al. The blood-brain barrier: an engineering perspective. Front. Neuroeng. 6, 7 (2013).

    Article  Google Scholar 

  34. Wang, X. Y. et al. Engineering interconnected 3D vascular networks in hydrogels using molded sodium alginate lattice as the sacrificial template. Lab Chip 14, 2709–2716 (2014).

    Article  CAS  Google Scholar 

  35. McAlpine, M. C., Ahmad, H., Wang, D. W. & Heath, J. R. Highly ordered nanowire arrays on plastic substrates for ultrasensitive flexible chemical sensors. Nature Mater. 6, 379–384 (2007).

    Article  CAS  Google Scholar 

  36. Annabi, N. et al. Hydrogel-coated microfluidic channels for cardiomyocyte culture. Lab Chip 13, 3569–3577 (2013).

    Article  CAS  Google Scholar 

  37. Wang, C. et al. User-interactive electronic skin for instantaneous pressure visualization. Nature Mater. 12, 899–904 (2013).

    Article  CAS  Google Scholar 

  38. Huang, Y., Duan, X. & Lieber, C. M. Nanowires for integrated multicolor nanophotonics. Small 1, 142–147 (2005).

    Article  CAS  Google Scholar 

  39. Takei, K. et al. Nanowire active-matrix circuitry for low-voltage macroscale artificial skin. Nature Mater. 9, 821–826 (2010).

    Article  CAS  Google Scholar 

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Acknowledgements

The authors thank R. Liao and D. Zhang for the inspiring discussion on cardiac electrophysiology and tissue engineering. The authors thank J. L. Huang for the assistance on instrumentation. This work was supported by National Institutes of Health Director's Pioneer and National Security Science and Engineering Faculty Fellow awards (to C.M.L.).

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Authors

Contributions

X.D., W.Z. and C.M.L. conceived and designed the experiments. X.D., W.Z., T.G. and J.L. performed the experiments and analysed the data. X.D., W.Z. and C.M.L. co-wrote the paper. All authors discussed the results and commented on the manuscript.

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Correspondence to Charles M. Lieber.

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The authors declare no competing financial interests.

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Dai, X., Zhou, W., Gao, T. et al. Three-dimensional mapping and regulation of action potential propagation in nanoelectronics-innervated tissues. Nature Nanotech 11, 776–782 (2016). https://doi.org/10.1038/nnano.2016.96

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