Spontaneous calcium waves in granule cells in cerebellar slice cultures

Neuroscience Letters

Volumn 553, Issue , 2013, Pages 78-83

  Apuschkin, Mia ^a   Ougaard, Maria ^a   Rekling, Jens C ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Axon guidance; Calcium waves; Cerebellum; Granule cells; Patterning

Indexed keywords

6 NITRO 7 SULFAMOYLBENZO[F]QUINOXALINE 2,3 DIONE; CALCIUM; DIZOCILPINE;

ANIMAL TISSUE; ARTICLE; BRAIN SLICE; BRAIN STEM; CALCIUM CELL LEVEL; CALCIUM SIGNALING; CEREBELLUM; EXCITATORY POSTSYNAPTIC POTENTIAL; GRANULE CELL; IMMUNOHISTOCHEMISTRY; INTRACELLULAR RECORDING; MOUSE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; SLICE CULTURE;

AXON GUIDANCE; CALCIUM WAVES; CEREBELLUM; GRANULE CELLS; PATTERNING;

ANIMALS; CALCIUM; CEREBELLUM; MICE; NEURONS; PATCH-CLAMP TECHNIQUES; RECEPTORS, AMPA; SYNAPTIC TRANSMISSION;

EID: 84884358724     PISSN: 03043940     EISSN: 18727972     Source Type: Journal    
DOI: 10.1016/j.neulet.2013.08.022     Document Type: Article

References (30)

1. Blankenship A.G., Feller M.B. Mechanisms underlying spontaneous patterned activity in developing neural circuits. Nat. Rev. Neurosci. 2010, 11:18-29.
2. Momose-Sato Y., Sato K., Kinoshita M. Spontaneous depolarization waves of multiple origins in the embryonic rat CNS. Eur. J. Neurosci. 2007, 25:929-944.
3. Torborg C.L., Feller M.B. Spontaneous patterned retinal activity and the refinement of retinal projections. Prog. Neurobiol. 2005, 76:213-235.
4. C.Gonzalez-Islas, Wenner P. Spontaneous network activity in the embryonic spinal cord regulates AMPAergic and GABAergic synaptic strength. Neuron 2006, 49:563-575.
5. Hanson M.G., Landmesser L.T. Normal patterns of spontaneous activity are required for correct motor axon guidance and the expression of specific guidance molecules. Neuron 2004, 43:687-701.
6. Garaschuk O., Linn J., Eilers J., Konnerth A. Large-scale oscillatory calcium waves in the immature cortex. Nat. Neurosci. 2000, 3:452-459.
7. Corlew R., Bosma M.M., Moody W.J. Spontaneous, synchronous electrical activity in neonatal mouse cortical neurones. J. Physiol. 2004, 560:377-390.
8. Sun J.J., Luhmann H.J. Spatio-temporal dynamics of oscillatory network activity in the neonatal mouse cerebral cortex. Eur. J. Neurosci. 2007, 26:1995-2004.
9. Yang J.W., Hanganu-Opatz I.L., Sun J.J., Luhmann H.J. Three patterns of oscillatory activity differentially synchronize developing neocortical networks in vivo. J. Neurosci. 2009, 29:9011-9025.
10. Allene C., Cattani A., Ackman J.B., Bonifazi P., Aniksztejn L., Ben-Ari Y., Cossart R. Sequential generation of two distinct synapse-driven network patterns in developing neocortex. J. Neurosci. 2008, 28:12851-12863.
11. Hoogland T.M., Kuhn B., Gobel W., Huang W., Nakai J., Helmchen F., Flint J., Wang S.S. Radially expanding transglial calcium waves in the intact cerebellum. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:3496-3501.
12. Mathiesen C., Brazhe A., Thomsen K., Lauritzen M. Spontaneous calcium waves in Bergman glia increase with age and hypoxia and may reduce tissue oxygen. J. Cereb. Blood Flow Metab. 2013, 33:161-169.
13. Nimmerjahn A., Mukamel E.A., Schnitzer M.J. Motor behavior activates Bergmann glial networks. Neuron 2009, 62:400-412.
14. Watt A.J., Cuntz H., Mori M., Nusser Z., Sjostrom P.J., Hausser M. Traveling waves in developing cerebellar cortex mediated by asymmetrical Purkinje cell connectivity. Nat. Neurosci. 2009, 12:463-473.
15. Kumada T., Komuro H. Completion of neuronal migration regulated by loss of Ca(2+) transients. Proc. Natl. Acad. Sci. U.S.A. 2004, 101:8479-8484.
16. Guan C.B., Xu H.T., Jin M., Yuan X.B., Poo M.M. Long-range Ca2+ signaling from growth cone to soma mediates reversal of neuronal migration induced by slit-2. Cell 2007, 129:385-395.
17. W.van I., Smith I.T., Watt A.J. The metamorphosis of the developing cerebellar microcircuit. Curr. Opin. Neurobiol. 2011, 21:245-253.
18. Morita D.F., Tominaga-Yoshino K., Ogura A. Survival promotion of rat cerebellar granule neurons by co-culture with pontine explant. Brain Res. 2003, 982:1-11.
19. Weyer A., Schilling K. Developmental and cell type-specific expression of the neuronal marker NeuN in the murine cerebellum. J. Neurosci. Res. 2003, 73:400-409.
20. Dusart I., Airaksinen M.S., Sotelo C. Purkinje cell survival and axonal regeneration are age dependent: an in vitro study. J. Neurosci. 1997, 17:3710-3726.
21. Scelfo B., Strata P. Correlation between multiple climbing fibre regression and parallel fibre response development in the postnatal mouse cerebellum. Eur. J. Neurosci. 2005, 21:971-978.
22. Dupont J.L., Fourcaudot E., Beekenkamp H., Poulain B., Bossu J.L. Synaptic organization of the mouse cerebellar cortex in organotypic slice cultures. Cerebellum 2006, 5:243-256.
23. Silver R.A., Traynelis S.F., Cull-Candy S.G. Rapid-time-course miniature and evoked excitatory currents at cerebellar synapses in situ. Nature 1992, 355:163-166.
24. Kirischuk S., Voitenko N., Kostyuk P., Verkhratsky A. Calcium signalling in granule neurones studied in cerebellar slices. Cell Calcium 1996, 19:59-71.
25. Mhyre T.R., Maine D.N., Holliday J. Calcium-induced calcium release from intracellular stores is developmentally regulated in primary cultures of cerebellar granule neurons. J. Neurobiol. 2000, 42:134-147.
26. Manzini I., Schweer T.S., Schild D. Improved fluorescent (calcium indicator) dye uptake in brain slices by blocking multidrug resistance transporters. J. Neurosci. Methods 2008, 167:140-147.
27. Meissirel C., Ruiz de A.C., Knevels E., Coulon C., Chounlamountri N., Segura I., de R.P., Vinckier S., Anthonis K., Deleglise B., de M.M., Ali C., Dassonville K., Loyens E., Honnorat J., Michotte Y., Rogemond V., Smolders I., Voets T., Vivien D., Vanden Berghe P., Van den Bosch L., Robberecht W., Chedotal A., Oliviero S., Dewerchin M., Schmucker D., Thomasset N., Salin P., Carmeliet P. VEGF modulates NMDA receptors activity in cerebellar granule cells through Src-family kinases before synapse formation. Proc. Natl. Acad. Sci. U.S.A. 2011, 108:13782-13787.
28. Scemes E., Giaume C. Astrocyte calcium waves: what they are and what they do. Glia 2006, 54:716-725.
29. Sieger D., Moritz C., Ziegenhals T., Prykhozhij S., Peri F. Long-range Ca2+ waves transmit brain-damage signals to microglia. Dev. Cell 2012, 22:1138-1148.
30. Hashimoto K., Yoshida T., Sakimura K., Mishina M., Watanabe M., Kano M. Influence of parallel fiber-Purkinje cell synapse formation on postnatal development of climbing fiber-Purkinje cell synapses in the cerebellum. Neuroscience 2009, 162:601-611.