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      Duration of complex-spikes grades Purkinje cell plasticity and cerebellar motor learning

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      1 , 1 , 2
      Nature

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          Abstract

          Behavioral learning is mediated by cellular plasticity such as changes in the strength of synapses at specific sites in neural circuits. The theory of cerebellar motor learning 1, 2, 3 relies on movement errors signaled by climbing-fiber inputs to cause long-term depression of synapses from parallel fibers to Purkinje cells 4, 5 . Yet, a recent review 6 has called into question the widely-held view that the climbing fiber input is an “all-or-none” event. In anesthetized animals, there is wide variation in the duration of the complex-spike (CS) caused in Purkinje cells by a climbing fiber input 7 . Further, the duration of electrically-controlled bursts in climbing fibers grades the amount of plasticity in Purkinje cells 8, 9 . The duration of bursts depends on the “state” of the inferior olive and therefore could be correlated across climbing fibers 8, 10 . Here, we provide a potential functional context for these mechanisms during motor learning in behaving monkeys. The magnitudes of both plasticity and motor learning depend on the duration of the CS responses. Further, the duration of CS responses appears to be a meaningful signal that is correlated across the Purkinje cell population during motor learning. We suggest that during learning, longer bursts in climbing fibers lead to longer duration CS responses in Purkinje cells, more calcium entry into Purkinje cells, larger synaptic depression, and stronger learning. The same graded impact of instructive signals for plasticity and learning could occur throughout the nervous system.

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          Most cited references33

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          A theory of cerebellar cortex.

          D. Marr (1969)
          1. A detailed theory of cerebellar cortex is proposed whose consequence is that the cerebellum learns to perform motor skills. Two forms of input-output relation are described, both consistent with the cortical theory. One is suitable for learning movements (actions), and the other for learning to maintain posture and balance (maintenance reflexes).2. It is known that the cells of the inferior olive and the cerebellar Purkinje cells have a special one-to-one relationship induced by the climbing fibre input. For learning actions, it is assumed that:(a) each olivary cell responds to a cerebral instruction for an elemental movement. Any action has a defining representation in terms of elemental movements, and this representation has a neural expression as a sequence of firing patterns in the inferior olive; and(b) in the correct state of the nervous system, a Purkinje cell can initiate the elemental movement to which its corresponding olivary cell responds.3. Whenever an olivary cell fires, it sends an impulse (via the climbing fibre input) to its corresponding Purkinje cell. This Purkinje cell is also exposed (via the mossy fibre input) to information about the context in which its olivary cell fired; and it is shown how, during rehearsal of an action, each Purkinje cell can learn to recognize such contexts. Later, when the action has been learnt, occurrence of the context alone is enough to fire the Purkinje cell, which then causes the next elemental movement. The action thus progresses as it did during rehearsal.4. It is shown that an interpretation of cerebellar cortex as a structure which allows each Purkinje cell to learn a number of contexts is consistent both with the distributions of the various types of cell, and with their known excitatory or inhibitory natures. It is demonstrated that the mossy fibre-granule cell arrangement provides the required pattern discrimination capability.5. The following predictions are made.(a) The synapses from parallel fibres to Purkinje cells are facilitated by the conjunction of presynaptic and climbing fibre (or post-synaptic) activity.(b) No other cerebellar synapses are modifiable.(c) Golgi cells are driven by the greater of the inputs from their upper and lower dendritic fields.6. For learning maintenance reflexes, 2(a) and 2(b) are replaced by2'. Each olivary cell is stimulated by one or more receptors, all of whose activities are usually reduced by the results of stimulating the corresponding Purkinje cell.7. It is shown that if (2') is satisfied, the circuit receptor --> olivary cell --> Purkinje cell --> effector may be regarded as a stabilizing reflex circuit which is activated by learned mossy fibre inputs. This type of reflex has been called a learned conditional reflex, and it is shown how such reflexes can solve problems of maintaining posture and balance.8. 5(a), and either (2) or (2') are essential to the theory: 5(b) and 5(c) are not absolutely essential, and parts of the theory could survive the disproof of either.
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            A theory of cerebellar function

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              Long-lasting depression of parallel fiber-Purkinje cell transmission induced by conjunctive stimulation of parallel fibers and climbing fibers in the cerebellar cortex.

              In rabbit cerebellar cortex, local stimulation of parallel fibers induced field potentials with two negative peaks, n1 representing conducting spikes of parallel fibers and n2 postsynaptic excitation in dendrites of Purkinje cells and other cortical cells. Conjunctive stimulation of parallel fibers and climbing fibers at 4 Hz for 30-120 sec caused a significant depression of n2 potential which lasted for at least 1 h. Such an effect could not be produced by stimulation of climbing fibers or parallel fibers alone. These observations support the plasticity assumption in the Marr-Albus model of the cerebellum.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                9 May 2014
                11 May 2014
                26 June 2014
                26 December 2014
                : 510
                : 7506
                : 529-532
                Affiliations
                [1 ]Department of Neurobiology, Duke University, Durham, NC, USA
                [2 ]Howard Hughes Medical Institute, Duke University, Durham, NC, USA
                Author notes
                Correspondence and requests for materials should be addressed to S.G.L. ( lisberger@ 123456neuro.duke.edu ) or Y.Y. ( yanyang@ 123456neuro.duke.edu )
                Proofs and correspondence to: Stephen G. Lisberger, Department of Neurobiology, 401 Research Drive, Room 327D, Durham, NC 27710, LISBERGER@ 123456neuro.duke.edu , Voice: (919) 681-7088
                Article
                NIHMS579567
                10.1038/nature13282
                4132823
                24814344
                7dbc038e-1e42-4e97-9f3a-fdb3e0c1ab1e
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