Unknown

Dataset Information

0

Emergence of stable striatal D1R and D2R neuronal ensembles with distinct firing sequence during motor learning.


ABSTRACT: The dorsolateral striatum (DLS) is essential for motor and procedure learning, but the role of DLS spiny projection neurons (SPNs) of direct and indirect pathways, as marked, respectively, by D1 and D2 receptor (D1R and D2R) expression, remains to be clarified. Long-term two-photon calcium imaging of the same neuronal population during mouse learning of a cued lever-pushing task revealed a gradual emergence of distinct D1R and D2R neuronal ensembles that reproducibly fired in a sequential manner, with more D1R and D2R neurons fired during the lever-pushing period and intertrial intervals (ITIs), respectively. This sequential firing pattern was specifically associated with the learned motor behavior, because it changed markedly when the trained mice performed other cued motor tasks. Selective chemogenetic silencing of D1R and D2R neurons impaired the initiation of learned motor action and suppression of erroneous lever pushing during ITIs, respectively. Thus, motor learning involves reorganization of DLS neuronal activity, forming stable D1R and D2R neuronal ensembles that fired sequentially to regulate different aspects of the learned behavior.

SUBMITTER: Sheng MJ 

PROVIDER: S-EPMC6561210 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Emergence of stable striatal D1R and D2R neuronal ensembles with distinct firing sequence during motor learning.

Sheng Meng-Jun MJ   Lu Di D   Shen Zhi-Ming ZM   Poo Mu-Ming MM  

Proceedings of the National Academy of Sciences of the United States of America 20190509 22


The dorsolateral striatum (DLS) is essential for motor and procedure learning, but the role of DLS spiny projection neurons (SPNs) of direct and indirect pathways, as marked, respectively, by D1 and D2 receptor (D1R and D2R) expression, remains to be clarified. Long-term two-photon calcium imaging of the same neuronal population during mouse learning of a cued lever-pushing task revealed a gradual emergence of distinct D1R and D2R neuronal ensembles that reproducibly fired in a sequential manner  ...[more]

Similar Datasets

| S-EPMC4474764 | biostudies-literature
| S-EPMC7166195 | biostudies-literature
| S-EPMC5127676 | biostudies-literature
| S-EPMC4495341 | biostudies-literature
| S-EPMC3455126 | biostudies-literature
| S-EPMC2930415 | biostudies-literature