Cbln1 is essential for synaptic integrity and plasticity in the cerebellum.

Nat Neurosci

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 332 North Lauderdale Street, MS 323, Memphis, Tennessee 38105-2794, USA.

Published: November 2005

Cbln1 is a cerebellum-specific protein of previously unknown function that is structurally related to the C1q and tumor necrosis factor families of proteins. We show that Cbln1 is a glycoprotein secreted from cerebellar granule cells that is essential for three processes in cerebellar Purkinje cells: the matching and maintenance of pre- and postsynaptic elements at parallel fiber-Purkinje cell synapses, the establishment of the proper pattern of climbing fiber-Purkinje cell innervation, and induction of long-term depression at parallel fiber-Purkinje cell synapses. Notably, the phenotype of cbln1-null mice mimics loss-of-function mutations in the orphan glutamate receptor, GluR delta2, a gene selectively expressed in Purkinje neurons. Therefore, Cbln1 secreted from presynaptic granule cells may be a component of a transneuronal signaling pathway that controls synaptic structure and plasticity.

Download full-text PDF

Source
http://dx.doi.org/10.1038/nn1576DOI Listing

Publication Analysis

Top Keywords

fiber-purkinje cell
12
granule cells
8
parallel fiber-purkinje
8
cell synapses
8
cbln1
4
cbln1 essential
4
essential synaptic
4
synaptic integrity
4
integrity plasticity
4
plasticity cerebellum
4

Similar Publications

C1q/TNF-related protein 14 (CTRP14), also known as C1q-like 1 (C1QL1), is a synaptic protein predominantly expressed in the brain. It plays a critical role in the formation and maintenance of the climbing fiber-Purkinje cell synapses, ensuring that only one single winning climbing fiber from the inferior olivary neuron synapses with the proximal dendrites of Purkinje cells during the early postnatal period. Loss of CTRP14/C1QL1 results in incomplete elimination of supernumerary climbing fibers, leading to multiple persistent climbing fibers synapsing with the Purkinje cells.

View Article and Find Full Text PDF

α2δ-2 regulates synaptic GluK1 kainate receptors in Purkinje cells and motor coordination.

Brain

October 2024

Center for Neuroscience and Pain Research, Department of Anesthesiology and Perioperative Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Article Synopsis
  • - Gabapentin and pregabalin, drugs used for neuropathic pain and epilepsy, interact with α2δ-2 proteins in the brain, which can lead to movement disorders, but the exact mechanisms are unclear.
  • - Research showed that α2δ-2 enhances the activity of GluK1 receptors, but pregabalin reduces this enhancement, indicating a complex relationship between these proteins.
  • - The study also found that blocking GluK1 receptors affected synaptic signals in Purkinje cells, and altering the interaction between α2δ-2 and GluK1 impacted overall receptor activity, suggesting potential pathways for managing drug side effects.
View Article and Find Full Text PDF

The effects of corticotropin-releasing factor on motor learning.

Sci Rep

July 2024

Institute of Innovative Science and Technology, Tokai University, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan.

Corticotropin-releasing factor (CRF) is mainly secreted from the hypothalamic paraventricular nuclei and plays a crucial role in stress-related responses. Recent studies have reported that CRF is a neuromodulator in the central nervous system. In the cerebellum, CRF is essential for the induction of long-term depression (LTD) at the parallel fiber-Purkinje cell synapses.

View Article and Find Full Text PDF

The enhancement of associative synaptic plasticity often results in impaired rather than enhanced learning. Previously, we proposed that such learning impairments can result from saturation of the plasticity mechanism (Nguyen-Vu et al., 2017), or, more generally, from a history-dependent change in the threshold for plasticity.

View Article and Find Full Text PDF

A Model with Dopamine Depletion in Basal Ganglia and Cerebellum Predicts Changes in Thalamocortical Beta Oscillations.

Int J Neural Syst

September 2024

NearLab, Department of Electronics, Information and Bioengineering (DEIB), Politecnico di Milano, Milano, Italy.

Parkinsonism is presented as a motor syndrome characterized by rigidity, tremors, and bradykinesia, with Parkinson's disease (PD) being the predominant cause. The discovery that those motor symptoms result from the death of dopaminergic cells in the substantia nigra led to focus most of parkinsonism research on the basal ganglia (BG). However, recent findings point to an active involvement of the cerebellum in this motor syndrome.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!