Skip to main content

In Vivo Functional Imaging of Retinal Neurons Using Red and Green Fluorescent Calcium Indicators

  • Conference paper
  • First Online:
Retinal Degenerative Diseases

Abstract

Adaptive optics retinal imaging of fluorescent calcium indicators is a minimally invasive method used to study retinal physiology over extended periods of time. It has potential for discovering novel retinal circuits, tracking retinal function in animal models of retinal disease, and assessing vision restoration therapy. We previously demonstrated functional adaptive optics imaging of retinal neurons in the living eye using green fluorescent calcium indicators; however, the use of green fluorescent indicators presents challenges that stem from the fact that they are excited by short-wavelength light. Using red fluorescent calcium indicators such as jRGECO1a, which is excited with longer-wavelength light (~560 nm), makes imaging approximately five times safer than using short-wavelength light (~500 nm) used to excite green fluorescent calcium indicators such as GCaMP6s. Red fluorescent indicators also provide alternative wavelength imaging regimes to overcome cross talk with the sensitivities of intrinsic photoreceptors and blue light-activated channelrhodopsins. Here we evaluate jRGECO1a for in vivo functional adaptive optics imaging of retinal neurons using single-photon excitation in mice. We find that jRGECO1a provides similar fidelity as the established green indicator GCaMP6s.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Chen TW, Wardill TJ, Sun Y et al (2013) Ultrasensitive fluorescent proteins for imaging neuronal activity. Nature 499:295–300

    Article  CAS  Google Scholar 

  • Dana H, Sun Y, Hasseman JP et al (2014) Improved red protein indicators for in vivo calcium imaging. In: Proceedings of the Society for Neuroscience, Washington DC

    Google Scholar 

  • Dana H, Mohar B, Sun Y et al (2016) Sensitive red protein calcium indicators for imaging neural activity. eLife 5:e12727

    Article  Google Scholar 

  • Dubra A, Harvey Z (2010) Registration of 2D images from fast scanning ophthalmic instruments. In: Biomedical image registration lecture notes in computer science. Springer, Berlin

    Google Scholar 

  • Geng Y, Dubra A, Yin L et al (2012) Adaptive optics retinal imaging in the living mouse eye. Biomed Opt Express 3:715–734

    Article  Google Scholar 

  • Ham WT Jr, Mueller HA, Sliney DH (1976) Retinal sensitivity to damage from short wavelength light. Nature 260:153–155

    Article  Google Scholar 

  • Hunter JJ, Morgan JI, Merigan WH et al (2012) The susceptibility of the retina to photochemical damage from visible light. Prog Retin Eye Res 31:28–42

    Article  Google Scholar 

  • Klapoetke NC, Murata Y, Kim SS et al (2014) Independent optical excitation of distinct neural populations. Nat Methods 11:338–346

    Article  CAS  Google Scholar 

  • Lin JY, Knutsen PM, Muller A et al (2013) ReaChR: a red-shifted variant of channelrhodopsin enables deep transcranial optogenetic excitation. Nat Neurosci 16:1499–1508

    Article  CAS  Google Scholar 

  • Lyubarsky AL, Falsini B, Pennesi ME et al (1999) UV- and midwave-sensitive cone-driven retinal responses of the mouse: a possible phenotype for coexpression of cone photopigments. J Neurosci 19:442–455

    Article  CAS  Google Scholar 

  • Nagel G, Szellas T, Huhn W et al (2003) Channelrhodopsin-2, a directly light-gated cation-selective membrane channel. Proc Natl Acad Sci U S A 100:13940–13945

    Article  CAS  Google Scholar 

  • Tomita H, Sugano E, Murayama N et al (2014) Restoration of the majority of the visual spectrum by using modified Volvox channelrhodopsin-1. Mol Ther J Am Soc Gene Ther 22:1434–1440

    Article  CAS  Google Scholar 

  • Walker MT, Brown RL, Cronin TW et al (2008) Photochemistry of retinal chromophore in mouse melanopsin. Proc Natl Acad Sci U S A 105:8861–8865

    Article  CAS  Google Scholar 

  • Wang YV, Weick M, Demb JB (2011) Spectral and temporal sensitivity of cone-mediated responses in mouse retinal ganglion cells. J Neurosci 31:7670–7681

    Article  CAS  Google Scholar 

  • Wu J, Seregard S, Algvere PV (2006) Photochemical damage of the retina. Surv Ophthalmol 51:461–481

    Article  Google Scholar 

  • Yin L, Geng Y, Osakada F et al (2013) Imaging light responses of retinal ganglion cells in the living mouse eye. J Neurophysiol 109:2415–2421

    Article  CAS  Google Scholar 

  • Yin L, Masella B, Dalkara D et al (2014) Imaging light responses of foveal ganglion cells in the living macaque eye. J Neurosci 34:6596–6605

    Article  CAS  Google Scholar 

  • Zhang J, Sabarinathan R, Bubel T et al (2016) Spectral dependence of light exposure on retinal pigment epithelium (RPE) disruption in living primate retina. Invest Ophthalmol Vis Sci 57:2220–2220

    Google Scholar 

Download references

Acknowledgements

We thank Sophia Zhao for making the jRGECO1a virus, Jie Zhang for designing and constructing the visual stimulus apparatus, and Keith Parkins for programing data acquisition software. This work was supported by grants from the National Eye Institute of the National Institutes of Health, EY001319 and EY021166; an Unrestricted Grant to the University of Rochester Department of Ophthalmology from Research to Prevent Blindness, New York, New York; as well as a Beckman-Argyros Award from the Arnold and Mabel Beckman Foundation. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The Genetically-Encoded Neuronal Indicator and Effector (GENIE) Project and the Janelia Farm Research Campus of the Howard Hughes Medical Institute have generously allowed these GECI materials to be distributed with the understanding that requesting investigators need to acknowledge the GENIE Program and the Janelia Farm Research Campus in any publication in which the material was used, specifically Vivek Jayaraman, PhD; Rex A. Kerr, PhD; Douglas S. Kim, PhD; Loren L. Looger, PhD; and Karel Svoboda, PhD from the GENIE Project, Janelia Farm Research Campus, Howard Hughes Medical Institute.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to William H. Merigan .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2018 Springer International Publishing AG, part of Springer Nature

About this paper

Check for updates. Verify currency and authenticity via CrossMark

Cite this paper

Cheong, S.K., Xiong, W., Strazzeri, J.M., Cepko, C.L., Williams, D.R., Merigan, W.H. (2018). In Vivo Functional Imaging of Retinal Neurons Using Red and Green Fluorescent Calcium Indicators. In: Ash, J., Anderson, R., LaVail, M., Bowes Rickman, C., Hollyfield, J., Grimm, C. (eds) Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology, vol 1074. Springer, Cham. https://doi.org/10.1007/978-3-319-75402-4_17

Download citation

Publish with us

Policies and ethics