4.8 Article

An Input-Specific Orphan Receptor GPR158-HSPG Interaction Organizes Hippocampal Mossy Fiber-CA3 Synapses

期刊

NEURON
卷 100, 期 1, 页码 201-+

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2018.08.038

关键词

-

资金

  1. CLME grant
  2. InfraMouse (KU Leuven-VIB) through a Hercules type 3 project [ZW09-03]
  3. FWO PhD fellowship [11Z3715N/17N]
  4. FWO postdoctoral fellowship [12N3515N]
  5. NIH [MH105482, DA026405, R00DC013805]
  6. ERC [311083]
  7. FWO Odysseus Grant
  8. FWO [G094016N, G0C4518N]
  9. Methusalem grant of KU Leuven/Flemish Government
  10. ERA-NET NEURON SynPathy 2015
  11. European Research Council (ERC) [311083] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Pyramidal neuron dendrites integrate synaptic input from multiple partners. Different inputs converging on the same dendrite have distinct structural and functional features, but the molecular mechanisms organizing input-specific properties are poorly understood. We identify the orphan receptor GPR158 as a binding partner for the heparan sulfate proteoglycan (HSPG) glypican 4 (GPC4). GPC4 is enriched on hippocampal granule cell axons (mossy fibers), whereas postsynaptic GPR158 is restricted to the proximal segment of CA3 apical dendrites receiving mossy fiber input. GPR158-induced presynaptic differentiation in contacting axons requires cell-surface GPC4 and the co-receptor LAR. Loss of GPR158 increases mossy fiber synapse density but disrupts bouton morphology, impairs ultrastructural organization of active zone and postsynaptic density, and reduces synaptic strength of this connection, while adjacent inputs on the same dendrite are unaffected. Our work identifies an input-specific HSPG-GPR158 interaction that selectively organizes synaptic architecture and function of developing mossy fiber-CA3 synapses in the hippocampus.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据