Skip to main content
Log in

Modulation of synchronous calcium oscillations in hippocampal neurons by photostimulation of astrocytes with femtosecond laser

  • Article
  • SPECIAL TOPIC: Huazhong University of Science and Technology Materials Science
  • Published:
Chinese Science Bulletin

Abstract

A large body of evidence indicates that astrocytes play an important role in a range of brain functions through calcium (Ca2+) signaling. Experimentally evoking Ca2+ signaling is a useful technique for investigating the functions of astrocytes. However, conventional stimulation methods typically have poor spatio-temporal precision, and some are invasive. Our group has developed a technique to overcome these problems, in which astrocytes are photostimulated with a femtosecond laser. In the current study, we applied this method to a hippocampal neural network to explore astrocytic functions in detail. The results revealed that applying photostimulation to astrocytes in a cultured hippocampal astrocyte-neuron network caused the following changes: (i) Synchronous Ca2+ oscillations in neurons were induced; (ii) spontaneous Ca2+ synchrony instantaneously emerged; and (iii) high-frequency spontaneous Ca2+ synchrony was regulated. Thus, astrocytic Ca2+ signaling evoked by photostimulation was found to modulate synchronous Ca2+ oscillations in hippocampal neurons. We propose that photostimulation with a femtosecond laser will serve as a powerful tool in investigating astrocytic functions at the network level.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Carmignoto G. Reciprocal communication systems between astrocytes and neurones. Prog Neurobiol, 2000, 62: 561–581

    Article  Google Scholar 

  2. Haydon P G, Carmignoto G. Astrocyte control of synaptic transmission and neurovascular coupling. Physiol Rev, 2006, 86: 1009–1031

    Article  Google Scholar 

  3. Nedergaard M, Ransom B, Goldman S A. New roles for astrocytes: Redefining the functional architecture of the brain. Trends Neurosci, 2003, 26: 523–530

    Article  Google Scholar 

  4. Schummers J, Yu H, Sur M. Tuned responses of astrocytes and their influence on hemodynamic signals in the visual cortex. Science, 2008, 320: 1638–1643

    Article  Google Scholar 

  5. Volterra A, Meldolesi J. Astrocytes, from brain glue to communication elements: the revolution continues. Nat Rev Neurosci, 2005, 6: 626–640

    Article  Google Scholar 

  6. Porter J T, McCarthy K D. Astrocytic neurotransmitter receptors in situ and in vivo. Prog Neurobiol, 1997, 51: 439–455

    Article  Google Scholar 

  7. Verkhratsky A, Orkand R K, Kettenmann H. Glial calcium: Homeostasis and signaling function. Physol Rev, 1998, 78: 99–141

    Google Scholar 

  8. Zhang Z, Chen G, Zhou W, et al. Regulated ATP release from astrocytes through lysosome exocytosis. Nat Cell Biol, 2007, 9: 945–953

    Article  Google Scholar 

  9. Jourdain P, Bergersen L H, Bhaukaurally K, et al. Glutamate exocytosis from astrocytes controls synaptic strength. Nat Neusci, 2007, 10: 331–339

    Article  Google Scholar 

  10. Mothet J-P, Pollegioni L, Ouanounou G, et al. Glutamate receptor activation triggers a calcium-dependent and SNARE protein-dependent release of the gliotransmitter D-serine. Proc Natl Acad Sci USA, 2005, 102: 5606–5611

    Article  Google Scholar 

  11. Charles A C, Merrill J E, Dirksen E R, et al. Intercellular signaling in glial cells: calcium waves and oscillations in response to mechanical stimulation and glutamate. Neuron, 1991, 6: 983–992

    Article  Google Scholar 

  12. Bernardinelli Y, Magistretti P J, Chatton J Y. Astrocytes generate Na+-mediated metabolic waves. Proc Natl Acad Sci USA, 2004, 101: 14937–14942

    Article  Google Scholar 

  13. Nedergaard M. Direct signaling from astrocytes to neurons in cultures of mammalian brain cells. Science, 1994, 263: 1768–1771

    Article  Google Scholar 

  14. Fiacco T A, McCarthy K D. Intracellular astrocyte calcium waves in situ increase the frequency of spontaneous AMPA receptor currents in CA1 pyramidal neurons. J Neurosci, 2004, 24: 722–732

    Article  Google Scholar 

  15. Leybaert L, Paemeleire K, Strahonja A, et al. Inositol-trisphosphate-dependent intercellular calcium signaling in and between astrocytes and endothelial cells. Glia, 1998, 24: 398–407

    Article  Google Scholar 

  16. Zhao Y, Zhang Y, Liu X, et al. Photostimulation of astrocytes with femtosecond laser pulses. Opt Express, 2009, 17: 1291–1298

    Article  Google Scholar 

  17. Vogel A, Noack J, Huttman G, et al. Mechanisms of femtosecond laser nanosurgery of cells and tissues. Appl Phys B, 2005, 81: 1015–1047

    Article  Google Scholar 

  18. Vogel A, Venugopalan V. Mechanisms of pulsed laser ablation of biological tissues. Chem Rev, 2003, 103: 577–644

    Article  Google Scholar 

  19. Tirlapur U K, König K. Femtosecond near-infrared laser pulses as a versatile non-invasive tool for intra-tissue nanoprocessing in plants without compromising viability. The Plant J, 2002, 31: 365–374

    Article  Google Scholar 

  20. Watanabe W, Matsunaga S, Fukui K, et al. Intracellular manipulation by femtosecond lasers: Review. J Innov Opt Health Sci, 2009, 2: 1–8

    Article  Google Scholar 

  21. Yanik M F, Cinar H, Cinar H N, et al. Functional regeneration after laser axotomy. Nature, 2004, 432: 822–822

    Article  Google Scholar 

  22. Zhou W, Liu X, Lv X, et al. Monitor and control of neuronal activities with femtosecond pulse laser. Chinese Sci Bull, 2008, 53: 687–694

    Article  Google Scholar 

  23. Gong J, Zhao X, Xing Q, et al. Femtosecond laser-induced cell fusion. Appl Phys Lett, 2008, 92: 093901

    Article  Google Scholar 

  24. Tirlapur U K, König K. Targeted transfection by femtosecond laser. Nature, 2002, 418: 290–291

    Article  Google Scholar 

  25. König K, Riemann I, Fritzsche W. Nanodissection of human chromosomes with near-infrared femtosecond laser pulses. Opt Lett, 2001, 26: 819–821

    Article  Google Scholar 

  26. Liu X, Lv X, Zeng S, et al. Noncontact and nondestructive identification of neural circuits with a femtosecond laser. Appl Phys Lett, 2009, 94: 061113

    Article  Google Scholar 

  27. Chen W, Li X, Pu J, et al. Nonlinear characteristics in the spontaneous activities of cultured neuronal networks (in Chinese). Chinese Sci Bull, 2010, 55: 7–14

    Article  Google Scholar 

  28. Lau P, Bi G. Reverberatory activity in neuronal networks in vitro. Chinese Sci Bull, 2009, 54: 1828–1835

    Article  Google Scholar 

  29. Corlew R, Bosma M M, Moody W J. Spontaneous, synchronous electrical activity in neonatal mouse cortical neurones. J Physiol, 2004, 560: 377–390

    Article  Google Scholar 

  30. Engel A K, Fries P, Singer W. Dynamic predictions: Oscillations and synchrony in top-down processing. Nat Rev Neurosci, 2001, 2: 704–716

    Article  Google Scholar 

  31. Schnitzler A, Gross J. Normal and pathological oscillatory communication in the brain. Nat Rev Neurosci, 2005, 6: 285–296

    Article  Google Scholar 

  32. Fellin T, Pascual O, Gobbo S, et al. Neuronal synchrony mediated by astrocytic glutamate through activation of extrasynaptic NMDA receptors. Neuron, 2004, 43: 729–743

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to ShaoQun Zeng.

About this article

Cite this article

Zhao, Y., Liu, X., Zhang, Y. et al. Modulation of synchronous calcium oscillations in hippocampal neurons by photostimulation of astrocytes with femtosecond laser. Chin. Sci. Bull. 55, 3436–3440 (2010). https://doi.org/10.1007/s11434-010-3376-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11434-010-3376-z

Keywords

Navigation