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Preparation and use of wireless reprogrammable multilateral optogenetic devices for behavioral neuroscience

Abstract

Wireless battery-free optogenetic devices enable behavioral neuroscience studies in groups of animals with minimal interference to natural behavior. Real-time independent control of optogenetic stimulation through near-field communication dramatically expands the realm of applications of these devices in broad contexts of neuroscience research. Dissemination of these tools with advanced functionalities to the neuroscience community requires protocols for device manufacturing and experimental implementation. This protocol describes detailed procedures for fabrication, encapsulation and implantation of recently developed advanced wireless devices in head- and back-mounted forms. In addition, procedures for standard implementation of experimental systems in mice are provided. This protocol aims to facilitate the application of wireless optogenetic devices in advanced optogenetic experiments involving groups of freely moving rodents and complex environmental designs. The entire protocol lasts ~3–5 weeks.

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Fig. 1: Flowchart of general procedures.
Fig. 2: Schematics of fabrication procedures for HM devices.
Fig. 3: Schematics of fabrication procedures for soft interconnections of BM devices.
Fig. 4: Schematics of encapsulation procedures for HM devices.
Fig. 5: Schematics of assembly procedures for BM devices.
Fig. 6: Viral transduction procedures in neonatal mice.
Fig. 7: Viral transduction procedures in adult mice.
Fig. 8: Implantation procedures for active HM devices.
Fig. 9: Implantation procedures for BM devices in mice.

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Data availability

No new data are presented in this paper. The circuit and serpentine design files are available at https://doi.org/10.5281/zenodo.559287318.

Code availability

The computer code for customized graphical user interface is available at https://doi.org/10.5281/zenodo.559287318.

References

  1. Shin, G. et al. Flexible near-field wireless optoelectronics as subdermal implants for broad applications in optogenetics. Neuron 93, 509–521.e3 (2017).

    Article  CAS  Google Scholar 

  2. Park, S. I. L. et al. Soft, stretchable, fully implantable miniaturized optoelectronic systems for wireless optogenetics. Nat. Biotechnol. 33, 1280–1286 (2015).

    Article  CAS  Google Scholar 

  3. McCall, J. G. et al. Fabrication and application of flexible, multimodal light-emitting devices for wireless optogenetics. Nat. Protoc. 8, 2413–2428 (2013).

    Article  CAS  Google Scholar 

  4. Montgomery, K. L. et al. Wirelessly powered, fully internal optogenetics for brain, spinal and peripheral circuits in mice. Nat. Methods 12, 969–974 (2015).

    Article  CAS  Google Scholar 

  5. Kim, T.-i et al. Injectable, cellular-scale optoelectronics with applications for wireless optogenetics. Science 340, 211–216 (2013).

    Article  CAS  Google Scholar 

  6. Pisanello, F. et al. Multipoint-emitting optical fibers for spatially addressable in vivo optogenetics. Neuron 82, 1245–1254 (2014).

    Article  CAS  Google Scholar 

  7. Wu, F. et al. Monolithically integrated μLEDs on silicon neural probes for high-resolution optogenetic studies in behaving animals. Neuron 88, 1136–1148 (2015).

    Article  CAS  Google Scholar 

  8. Mickle, A. D. et al. A wireless closed-loop system for optogenetic peripheral neuromodulation. Nature 565, 361–365 (2019).

    Article  CAS  Google Scholar 

  9. Hibberd, T. J. et al. Optogenetic induction of colonic motility in mice. Gastroenterology 155, 514–528.e6 (2018).

    Article  Google Scholar 

  10. Gutruf, P. et al. Fully implantable optoelectronic systems for battery-free, multimodal operation in neuroscience research. Nat. Electron. 1, 652–660 (2018).

    Article  Google Scholar 

  11. Gutruf, P. & Rogers, J. A. Implantable, wireless device platforms for neuroscience research. Curr. Opin. Neurobiol. 50, 42–49 (2017).

    Article  Google Scholar 

  12. McCall, J. G. et al. Preparation and implementation of optofluidic neural probes for in vivo wireless pharmacology and optogenetics. Nat. Protoc. 12, 219–237 (2017).

    Article  CAS  Google Scholar 

  13. Burton, A. et al. Wireless, battery-free subdermally implantable photometry systems for chronic recording of neural dynamics. Proc. Natl Acad. Sci. USA 117, 2835–2845 (2020).

    Article  CAS  Google Scholar 

  14. Yang, Y. et al. Wireless multilateral devices for optogenetic studies of individual and social behaviors. Nat. Neurosci. 24, 1035–1045 (2021).

    Article  CAS  Google Scholar 

  15. Kale, R. P., Kouzani, A. Z., Walder, K., Berk, M. & Tye, S. J. Evolution of optogenetic microdevices. Neurophotonics 2, 031206 (2015).

    Article  Google Scholar 

  16. Sidor, M. M. et al. In vivo optogenetic stimulation of the rodent central nervous system. J. Vis. Exp. https://doi.org/10.3791/51483 (2015).

  17. Etter, G. et al. Optogenetic gamma stimulation rescues memory impairments in an Alzheimer’s disease mouse model. Nat. Commun. 10, 5322 (2019).

    Article  Google Scholar 

  18. Yang, Y. et al. Preparation and use of wireless reprogrammable multilateral optogenetic devices for behavioral neuroscience. Smart NFC Optogenetics https://doi.org/10.5281/zenodo.5592873 (2021).

  19. Owen, S. F., Liu, M. H. & Kreitzer, A. C. Thermal constraints on in vivo optogenetic manipulations. Nat. Neurosci. 22, 1061–1065 (2019).

    Article  CAS  Google Scholar 

  20. Zhang, F. et al. The microbial opsin family of optogenetic tools. Cell 147, 1446–1457 (2011).

    Article  CAS  Google Scholar 

  21. Wu, M. et al. Attenuated dopamine signaling after aversive learning is restored by ketamine to rescue escape actions. eLife 10, e64041 (2021).

    Article  CAS  Google Scholar 

  22. Wu, M., Minkowicz, S., Dumrongprechachan, V., Hamilton, P. & Kozorovitskiy, Y. Ketamine rapidly enhances glutamate-evoked dendritic spinogenesis in medial prefrontal cortex through dopaminergic mechanisms. Biol. Psychiatry 89, 1096–1105 (2021).

    Article  CAS  Google Scholar 

  23. Ausra, J. et al. Wireless, battery-free, subdermally implantable platforms for transcranial and long-range optogenetics in freely moving animals. Proc. Natl Acad. Sci. USA 118, e2025775118 (2021).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work utilized Northwestern University Micro/Nano Fabrication Facility (NUFAB), which is partially supported by Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205), the Materials Research Science and Engineering Center (DMR-1720139), the State of Illinois, and Northwestern University. C.H.G. is supported by the LUCI program, sponsored by the Basic Research Office, Office of Under Secretary of Defense for Research and Engineering (USD R&E). Y.K. is supported by the NIH R01MH117111 and R01NS107539, and Beckman Young Investigator Award. M.W is supported as an affiliate fellow of the NIH T32 AG20506 and 2021 Christina Enroth-Cugell and David Cugell Fellow. Z.X. acknowledges the support from the National Natural Science Foundation of China (grant no. 12072057), LiaoNing Revitalization Talents Program (grant no. XLYC2007196) and Fundamental Research Funds for the Central Universities (grant no. DUT20RC(3)032). Y.H. acknowledges support from NSF (CMMI1635443).

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Authors and Affiliations

Authors

Contributions

Y.Y., M.W., A.J.W., A.V.-G., Z.X., C.H.G., Y.K. and J.A.R. contributed ideas and designed research. Y.Y., A.V.-G., C.H.G. and J.A.R. proposed the device platform. M.W., A.J.W., C.H.G. and Y.K. developed and performed the device implantation. A.V.-G. and Y.Y. established the electronic system. Y.Y., M.W., A.J.W., A.V.-G., A.I.E., F.L., T.W., Y.M., A.B., Z.L., Z.X. and C.H.G. performed experiments. Y.Y., M.W., A.J.W., A.V.-G., C.H.G., Y.H., Y.K. and J.A.R. wrote the paper with input from other authors.

Corresponding authors

Correspondence to Cameron H. Good, Yevgenia Kozorovitskiy or John A. Rogers.

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Competing interests

J.A.R. and A.B. are cofounders in a company, Neurolux, Inc., that offers related technology products to the neuroscience community.

Peer review

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Nature Protocols thanks Seongjun Park and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

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Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Key reference using this protocol

Yang, Y. et al. Nat. Neurosci. 24, 1035–1045 (2021): https://doi.org/10.1038/s41593-021-00849-x

Extended data

Extended Data Fig. 1 Preparation of the electronic module and probes.

a, Apply laser ablation to form the geometrical layouts and circuit footprints for electronic modules and probes. b, Use ultrasonic flux bath to clean the surfaces of modules and probes after laser ablation. ce, Fill in laser-ablated via holes with liquid silver paint using a 30 gauge blunt needle to make electrical connections between top and bottom circuits: active HM device (c), BM module (d), passive HM device (e) and probes for BM devices (f). gj, Solder electronic components on circuit footprint: active HM device (g), BM module (h), passive HM device (i), probes for BM devices (j). km, Device operation: passive HM device (k), active HM device (l), BM module (m).

Extended Data Fig. 2 Attiny84 microcontroller programming using Arduino IDE.

The microcontroller is programmed using open-source Arduino software, commercial ISP programmer and QFN20 packaging adapter socket. (i) Open the microcontroller firmware using Arduino. Set the corresponding programming parameters. (ii) Connect the programmer to the computer. (iii) Mount the microcontroller chip onto the QFN20 socket and secure properly. Upload the firmware to the microcontroller.

Extended Data Fig. 3 Preparation of soft interconnections for back-mounted devices.

a, Apply photolithographic method to define the serpentine geometries for metallic and SiO2 layers. b, Use RIE to define the serpentine geometries of parylene encapsulation layers. The contact pads are exposed for electrical connections. cf, Transfer printing process: cover the silicon wafer with a thin wipe (Kimtech) and another same-sized silicon wafer, and put it in an acetone bath heated by a hotplate at 80 °C for 120 min (c); use water-soluble tape to transfer the interconnection traces from silicon substrate (d); bond the interconnection traces on silicone substrate (e); dissolve tape in distilled water (f).

Extended Data Fig. 4 Preparation of tungsten strengthened probes.

ac, Glue tungsten stiffeners on the active HM device (a), the passive HM device (b) and the probe for BM device (c). Scale bars, 5 mm.

Extended Data Fig. 5 PDMS coatings for HM devices.

a, Use a sharp tweezer to dip PDMS droplets to cover the coils, electronic components, serpentine connections, and probes of an active HM device lying on a flat stage. b, Same dip coating process applied at top side of a passive HM device. c, Same dip coating process applied at back side of an active HM device. d, Same dip coating process applied at back side of a passive HM device. Scale bars, 5 mm.

Extended Data Fig. 6 Assembly of back-mounted devices.

a, Cover the BM module and probe with PI shadow mask with contact pads exposed. RIE process removes the parylene coatings on contact pads, allowing future electrical connections among these components. b, Solder the probe on soft interconnection traces (left). Verify the electrical connections by powering the µ-ILED with multimeter (right). c, Solder the soft interconnection traces on the BM module to complete the assembly. d, Encapsulate the solder joints with epoxy. The joints include the back side of the probe’s flag (top left), top side of the ends of soft serpentine traces (bottom left), top side of the probe’s flag (top right) and back side of the ends of soft serpentine traces (bottom right). e, Use a sharp tweezer to dip Ecoflex droplets on the top side of serpentine traces followed by thermal curing. Then dip PDMS droplets on top side of the BM module and back side of probes (the side with the tungsten stiffeners) followed by thermal curing. f, Similar dip coating process with PDMS droplets is applied at the back side of the BM device including the back side of the electronic module and the front side of the probes (with µ-ILEDs). Scale bar, 5 mm.

Extended Data Fig. 7 Implantation procedures for passive HM devices.

a, Clamp the first probe. b, Prepare the surgical space, make an incision, confirm the implantation coordinates and drill insertion holes. c, Insert the first probe. d,e, Use dental cement to fix the injected probe. f, Insert the second probe. g, fix the position of the second probe, and withdraw the probe holder. h, Suture the skin, and proceed with postoperative steps and monitoring according to institutional guidelines.

Extended Data Fig. 8 Experimental implementation.

a, Block diagram that indicates the implementation of the typical wireless optogenetics system. The graphic user interface (GUI) is hosted on a computer and interfaces with the power distribution controller (PDB) via serial interface. The PDB box drives radio frequency power at 13.56 MHz to the transmitting antenna on the experimental enclosure and transfers wireless power to the receiving antennae on the NFC devices. The impedance of the transmission antenna is properly matched using an impedance tuner (Tuner). The PDB, besides providing RF power, also relays read/write commands instructed from the GUI to the NFC device as the basis of wireless control of the mode of operation of the implantable devices. b, Photograph of a typical experimental implementation showing the hardware described in a.

Extended Data Fig. 9 Implementation of a generic wireless power transfer system for passive and active devices.

a, Block diagram that shows the implementation of the RF system for operating passive devices. b, Block diagram that shows the implementation of a system for operating smart NFC devices.

Extended Data Fig. 10 Graphic user interface.

a, Screenshot of the GUI designed to control multiple devices sharing the same experimental arena. The GUI connects to the PDB box using commands in block (i). Commands in block (ii) allow the detection of devices in the RF field (Inventory) which are then listed in dropdown menu (Device list). The command ‘Read summary’ interrogates the selected devices and provides a summary of the parameters currently stored in the device’s memory (see b). Commands in block (iii) read (Read) and write (Write) parameters such as Frequency, Pulse width and Burst period to the selected device and selected mode of operation. Commands in block (iv) provide access to the mode of operation of the devices. Options such as Single or Dual mode of operation, as well as the channel selection or tonic or burst stimulation modes, are specified here. Commands in block (v) provides access to the RF parameters of the PDB box, such as power setting or toggling the operation status of the RF field, i.e., ON/OFF operation. Finally, block (vi) shows a snapshot of the waveform that the device will produce based on the parameters specified in blocks (iii) and (iv). b, Screenshot of the configuration summary currently stored in the memory of the device produced when hitting the ‘Read summary’ command button in block (ii). If the experiment does not require further adjustment of these parameters, only commands such as those specified in block (iv) will need subsequent changes.

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Yang, Y., Wu, M., Wegener, A.J. et al. Preparation and use of wireless reprogrammable multilateral optogenetic devices for behavioral neuroscience. Nat Protoc 17, 1073–1096 (2022). https://doi.org/10.1038/s41596-021-00672-5

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