Abstract
Since 1990s, long-term depression of (LTD) at parallel fiber–Purkinje cell synapses has been regarded as a cellular phenomenon for motor learning. However, parallel fiber LTD by itself cannot account for motor learning. Here, we review a rich variety of use-dependent plasticity in the cerebellar cortex and nuclei, including long-term potentiation (LTP) and LTD at excitatory and inhibitory synapses, and persistent modulation of intrinsic excitability. Prevailing studies demonstrated that intrinsic and extrinsic factors, including neuronal excitation, specific molecular mechanisms, theta oscillation, and external neuromodulators, are essential to different forms of plasticity in the cerebellum.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Aizenman CD, Manis PB, Linden DJ (1998) Polarity of long-term synaptic gain change is related to postsynaptic spike firing at a cerebellar inhibitory synapse. Neuron 21:827–835
Aizenman CD, Huang EJ, Linden DJ (2003) Morphological correlates of intrinsic electrical excitability in neurons of the deep cerebellar nuclei. J Neurophysiol 89:1738–1747
Bear MF, Linden DJ (2000) The mechanisms and meaning of long-term synaptic depression in the mammalian brain. In: Cowan WM, Davies K (eds) The synapse. Johns Hopkins Univ Press, Baltimore, MD, pp 455–516
Bouvier G, Higgins D, Spolidoro M et al (2016) Burst-dependent bidirectional plasticity in the cerebellum is driven by presynaptic NMDA receptors. Cell Rep 15:104–116
Coesmans M, Weber JT, De Zeeuw CI et al (2004) Bidirectional parallel fiber plasticity in the cerebellum under climbing fiber control. Neuron 44:691–700
D’Angelo E, Rossi P, Armano S et al (1999) Evidence for NMDA and mGlu receptor-dependent long-term potentiation of mossy fibre–granule cell transmission in rat cerebellum. J Neurophysiol 81:277–287
Ekerot CF, Kano M (1989) Stimulation parameters influencing climbing fibre induced long-term depression of parallel fibre synapses. Neurosci Res 6:264–268.
Gall D, Prestori F, Sola E et al (2005) Intracellular calcium regulation by burst discharge determines bidirectional longterm synaptic plasticity at the cerebellum input stage. J Neurosci 25:4813–4822
Grasselli G, Boele HJ, Titley HK et al (2020) SK2 channels in cerebellar Purkinje cells contribute to excitability modulation in motor-learning-specific memory traces. PLoS Biol 18:e3000596
Gutierrez-Castellanos N, Da Silva-Matos CM, Zhou K et al (2017) Motor learning requires Purkinje cell synaptic potentiation through activation of AMPA-receptor subunit GluA3. Neuron 93:409–424
Hansel C, Linden DJ (2000) Long-term depression of the cerebellar climbing fiber-Purkinje neuron synapse. Neuron 26:473–482
Hansel C, Linden DJ, D’Angelo E (2001) Beyond parallel fiber LTD: the diversity of synaptic and nonsynaptic plasticity in the cerebellum. Nat Neurosci 4:467–475
Häusser M, Clark BA (1997) Tonic synaptic inhibition modulates neuronal output pattern and spatiotemporal synaptic integration. Neuron 19:665–678
Ito M, Sakurai M, Tongroach P (1982) Climbing fiber induced depression of both mossy fiber responsiveness and glutamate sensitivity of cerebellar Purkinje cells. J Physiol Lond 324:113–134
Jang DC, Shim HG, Kim SJ (2020) Intrinsic plasticity of cerebellar Purkinje cells contributes to motor memory consolidation. J Neurosci 40:4145–4157
Kano M (1996) Long-lasting potentiation of GABAergic inhibitory synaptic transmission in cerebellar Purkinje cells: its properties and possible mechanisms. Behav Brain Sci 19:354–361
Kano M, Rexhausen U, Dreessen J et al (1992) Synaptic excitation produces a long-lasting rebound potentiation of inhibitory synaptic signals in cerebellar Purkinje cells. Nature 356:601–604
Kawaguchi S, Hirano T (2000) Suppression of inhibitory synaptic potentiation by presynaptic activity through postsynaptic GABAB receptors in a Purkinje neuron. Neuron 27:339–347
Kono M, Kakegawa W, Yoshida K et al (2019) Interneuronal NMDA receptors regulate long-term depression and motor learning in the cerebellum. J Physiol 597:903–920
Libster AM, Title B, Yarom Y (2015) Corticotropin-releasing factor increases Purkinje neuron excitability by modulating sodium, potassium, and Ih currents. J Neurophysiol 114:3339–3350
Linden DJ (1998) Synaptically-evoked glutamate transport currents may be used to detect the expression of long-term potentiation in cerebellar culture. J Neurophysiol 79:3151–3156
Lippiello P, Hoxha E, Speranza L et al (2016) The 5-HT7 receptor triggers cerebellar long-term synaptic depression via PKC-MAPK. Neuropharmacology 101:426–438
Lonart G, Schoch S, Kaeser PS et al (2003) Phosphorylation of RIM1alpha by PKA triggers presynaptic long-term potentiation at cerebellar parallel fiber synapses. Cell 115:49–60
Mark MD, Krause M, Boele HJ et al (2015) Spinocerebellar ataxia type 6 protein aggregates cause deficits in motor learning and cerebellar plasticity. J Neurosci 35:8882–8895
MartÃn R, GarcÃa-Font N, Suárez-Pinilla AS et al (2020) β-Adrenergic receptors/Epac signaling increases the size of the readily releasable pool of synaptic vesicles required for parallel fiber LTP. J Neurosci 40:8604–8617
Piochon C, Kruskal P, Maclean J, Hansel C (2013) Non-Hebbian spike-timing-dependent plasticity in cerebellar circuits. Front Neural Circuits 6:124
Pugh JR, Raman IM (2006) Potentiation of mossy fiber EPSCs in the cerebellar nuclei by NMDA receptor activation followed by postinhibitory rebound current. Neuron 51:113–123
Ryu C, Jang DC, Jung D et al (2017) STIM1 regulates somatic Ca2+ signals and intrinsic firing properties of cerebellar Purkinje neurons. J Neurosci 37:8876–8894
Safo PK, Regehr WG (2005) Endocannabinoids control the induction of cerebellar LTD. Neuron 48:647–659
Salin PA, Malenka RC, Nicoll RA (1996) cAMP mediates a presynaptic form of LTP at cerebellar parallel fiber synapses. Neuron 16:797–803
Serulle Y, Zhang S, Ninan I et al (2007) A GluR1-cGKII interaction regulates AMPA receptor trafficking. Neuron 56:670–688
Shen Y, Linden DJ (2005) Long-term potentiation of neuronal glutamate transporters. Neuron 46:715–722
Shen Y, Hansel C, Linden DJ (2002) Glutamate release during LTD at cerebellar climbing fiber-Purkinje cell synapses. Nat Neurosci 5:725–726
Shim HG, Jang SS, Jang DC et al (2016) mGlu1 receptor mediates homeostatic control of intrinsic excitability through Ih in cerebellar Purkinje cells. J Neurophysiol 115:2446–2455
Tsai PT, Hull C, Chu Y et al (2012) Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice. Nature 488:647–651
Wang YT, Linden DJ (2000) Expression of cerebellar long-term depression requires postsynaptic clathrin-mediated endocytosis. Neuron 25:635–647
Wang DJ, Su LD, Wang YN et al (2014) Long-term potentiation at cerebellar parallel fiber-Purkinje cell synapses requires presynaptic and postsynaptic signaling cascades. J Neurosci 34:2355–2364
Yamamoto M, Kim M, Imai H et al (2019) Microglia-triggered plasticity of intrinsic excitability modulates psychomotor behaviors in acute cerebellar inflammation. Cell Rep 28:2923–2938
Zhou L, Yang D, Wang DJ et al (2015) Numb deficiency in cerebellar Purkinje cells impairs synaptic expression of metabotropic glutamate receptor and motor coordination. Proc Natl Acad Sci U S A 112:15474–15479
Zhou JH, Wang XT, Zhou L et al (2017) Ablation of TFR1 in Purkinje cells inhibits mGlu1 trafficking and impairs motor coordination, but not autistic-like behaviors. J Neurosci 37:11335–11352
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2023 The Author(s), under exclusive license to Springer Nature Switzerland AG
About this chapter
Cite this chapter
Wang, XT., Shen, Y. (2023). Plasticity of the Cerebellum. In: Gruol, D.L., Koibuchi, N., Manto, M., Molinari, M., Schmahmann, J.D., Shen, Y. (eds) Essentials of Cerebellum and Cerebellar Disorders. Springer, Cham. https://doi.org/10.1007/978-3-031-15070-8_43
Download citation
DOI: https://doi.org/10.1007/978-3-031-15070-8_43
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-031-15069-2
Online ISBN: 978-3-031-15070-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)