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LRRTM4:调控视网膜双极细胞突触前抑制和带状突触排列的新型调节蛋白。

LRRTM4: A Novel Regulator of Presynaptic Inhibition and Ribbon Synapse Arrangements of Retinal Bipolar Cells.

机构信息

Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, Madison, USA; McPherson Eye Research Institute, University of Wisconsin, Madison, WI, USA; Department of Physiology and Biophysics, University of Washington, Seattle, WA, USA.

Department of Physiology and Pathophysiology, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3E 0J9, Canada; Neuroscience Research Program, Kleysen Institute for Advanced Medicine, Health Sciences Center, Winnipeg, MB R3E 0Z3, Canada; The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.

出版信息

Neuron. 2020 Mar 18;105(6):1007-1017.e5. doi: 10.1016/j.neuron.2019.12.028. Epub 2020 Jan 20.

Abstract

LRRTM4 is a transsynaptic adhesion protein regulating glutamatergic synapse assembly on dendrites of central neurons. In the mouse retina, we find that LRRTM4 is enriched at GABAergic synapses on axon terminals of rod bipolar cells (RBCs). Knockout of LRRTM4 reduces RBC axonal GABA and GABA receptor clustering and disrupts presynaptic inhibition onto RBC terminals. LRRTM4 removal also perturbs the stereotyped output synapse arrangement at RBC terminals. Synaptic ribbons are normally apposed to two distinct postsynaptic "dyad" partners, but in the absence of LRRTM4, "monad" and "triad" arrangements are also formed. RBCs from retinas deficient in GABA release also demonstrate dyad mis-arrangements but maintain LRRTM4 expression, suggesting that defects in dyad organization in the LRRTM4 knockout could originate from reduced GABA receptor function. LRRTM4 is thus a key synapse organizing molecule at RBC terminals, where it regulates function of GABAergic synapses and assembly of RBC synaptic dyads.

摘要

LRRTM4 是一种跨突触黏附蛋白,可调节中枢神经元树突上的谷氨酸能突触组装。在小鼠视网膜中,我们发现 LRRTM4 在杆状双极细胞 (RBC) 轴突末梢上的 GABA 能突触中富集。LRRTM4 的缺失减少了 RBC 轴突 GABA 和 GABA 受体的聚集,并破坏了 RBC 末梢上的突触前抑制。LRRTM4 的去除也扰乱了 RBC 末梢上定型的输出突触排列。突触带通常与两个不同的突触后“二联体”伙伴相对,但在没有 LRRTM4 的情况下,也会形成“单体”和“三联体”排列。缺乏 GABA 释放的视网膜中的 RBC 也表现出二联体排列异常,但仍保持 LRRTM4 的表达,这表明 LRRTM4 缺失中的二联体组织缺陷可能源于 GABA 受体功能的降低。因此,LRRTM4 是 RBC 末梢处的关键突触组织分子,它调节 GABA 能突触的功能和 RBC 突触二联体的组装。

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