Adhesion GPCR Latrophilin 3 regulates synaptic function of cone photoreceptors in a trans-synaptic manner

被引:2
|
作者
Wang, Yuchen [1 ]
Cao, Yan [1 ]
Hays, Cassandra L. [2 ]
Laboute, Thibaut [1 ]
Ray, Thomas A. [3 ]
Guerrero-Given, Debbie [4 ]
Ahuja, Abhimanyu S. [1 ]
Patil, Dipak [1 ]
Rivero, Olga [5 ]
Kamasawa, Naomi [4 ]
Kay, Jeremy N. [3 ]
Thoreson, Wallace B. [2 ]
Martemyanov, Kirill A. [1 ]
机构
[1] Scripps Res Inst, Dept Neurosci, Jupiter, FL 33458 USA
[2] Univ Nebraska Med Ctr, Durham Res Ctr 1, Truhlsen Eye Inst, Omaha, NE 68198 USA
[3] Duke Univ, Sch Med, Dept Neurobiol & Ophthalmol & Cell Biol, Durham, NC 27710 USA
[4] Max Planck Florida Inst, Electron Microscopy Core Facil, Jupiter, FL 33458 USA
[5] Univ Wurzburg, Ctr Mental Hlth, Div Mol Psychiat, D-97080 Wurzburg, Germany
关键词
retina; adhesion GPCR; synapses; horizontal cells; vision; HORIZONTAL CELLS; STRUCTURAL BASIS; EXOCYTOSED PROTONS; PEANUT AGGLUTININ; RIBBON SYNAPSE; GENE; FEEDBACK; BINDING; RETINA; LIGHT;
D O I
10.1073/pnas.2106694118
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cone photoreceptors mediate daylight vision in vertebrates. Changes in neurotransmitter release at cone synapses encode visual information and is subject to precise control by negative feedback from enigmatic horizontal cells. However, the mechanisms that orchestrate this modulation are poorly understood due to a virtually unknown landscape of molecular players. Here, we report a molecular player operating selectively at cone synapses that modulates effects of horizontal cells on synaptic release. Using an unbiased proteomic screen, we identified an adhesion GPCR Latrophilin3 (LPHN3) in horizontal cell dendrites that engages in transsynaptic control of cones. We detected and characterized a prominent splice isoform of LPHN3 that excludes a element with inhibitory influence on transsynaptic interactions. A gain-of-function mouse model specifically routing LPHN3 splicing to this isoform but not knockout of LPHN3 diminished Ca(v)1.4 calcium channel activity profoundly disrupted synaptic release by cones and resulted in synaptic transmission deficits. These findings offer molecular insight into horizontal cell modulation on cone synaptic function and more broadly demonstrate the importance of alternative splicing in adhesion GPCR5 for their physiological function.
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页数:12
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