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000162869 037__ $$aDZNE-2021-01524
000162869 041__ $$aEnglish
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000162869 1001_ $$00000-0002-6073-8811$$aEmmenegger, Marc$$b0
000162869 245__ $$aLAG3 is not expressed in human and murine neurons and does not modulate α-synucleinopathies.
000162869 260__ $$aHeidelberg$$bEMBO Press$$c2021
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000162869 520__ $$aWhile the initial pathology of Parkinson's disease and other α-synucleinopathies is often confined to circumscribed brain regions, it can spread and progressively affect adjacent and distant brain locales. This process may be controlled by cellular receptors of α-synuclein fibrils, one of which was proposed to be the LAG3 immune checkpoint molecule. Here, we analysed the expression pattern of LAG3 in human and mouse brains. Using a variety of methods and model systems, we found no evidence for LAG3 expression by neurons. While we confirmed that LAG3 interacts with α-synuclein fibrils, the specificity of this interaction appears limited. Moreover, overexpression of LAG3 in cultured human neural cells did not cause any worsening of α-synuclein pathology ex vivo. The overall survival of A53T α-synuclein transgenic mice was unaffected by LAG3 depletion, and the seeded induction of α-synuclein lesions in hippocampal slice cultures was unaffected by LAG3 knockout. These data suggest that the proposed role of LAG3 in the spreading of α-synucleinopathies is not universally valid.
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000162869 650_7 $$2Other$$aLAG3
000162869 650_7 $$2Other$$aneurodegeneration
000162869 650_7 $$2Other$$aprionoids
000162869 650_7 $$2Other$$aα-synuclein
000162869 650_7 $$2NLM Chemicals$$aalpha-Synuclein
000162869 650_2 $$2MeSH$$aAnimals
000162869 650_2 $$2MeSH$$aHumans
000162869 650_2 $$2MeSH$$aMice
000162869 650_2 $$2MeSH$$aMice, Transgenic
000162869 650_2 $$2MeSH$$aNeurons
000162869 650_2 $$2MeSH$$aParkinson Disease
000162869 650_2 $$2MeSH$$aSynucleinopathies
000162869 650_2 $$2MeSH$$aalpha-Synuclein: genetics
000162869 7001_ $$00000-0002-0148-2596$$aDe Cecco, Elena$$b1
000162869 7001_ $$00000-0002-9253-4362$$aHruska-Plochan, Marian$$b2
000162869 7001_ $$0P:(DE-2719)2811141$$aEninger, Timo$$b3$$udzne
000162869 7001_ $$00000-0002-1894-1859$$aSchneider, Matthias M$$b4
000162869 7001_ $$0P:(DE-2719)2812097$$aBarth, Melanie$$b5$$udzne
000162869 7001_ $$00000-0001-9189-3390$$aTantardini, Elena$$b6
000162869 7001_ $$ade Rossi, Pierre$$b7
000162869 7001_ $$0P:(DE-2719)2810940$$aBacioglu, Mehtap$$b8$$udzne
000162869 7001_ $$aLangston, Rebekah G$$b9
000162869 7001_ $$aKaganovich, Alice$$b10
000162869 7001_ $$00000-0002-3700-0464$$aBengoa-Vergniory, Nora$$b11
000162869 7001_ $$aGonzalez-Guerra, Andrès$$b12
000162869 7001_ $$00000-0003-4665-5558$$aAvar, Merve$$b13
000162869 7001_ $$00000-0002-3282-4042$$aHeinzer, Daniel$$b14
000162869 7001_ $$aReimann, Regina$$b15
000162869 7001_ $$0P:(DE-2719)2811581$$aHäsler, Lisa M$$b16$$udzne
000162869 7001_ $$aHerling, Therese W$$b17
000162869 7001_ $$aMatharu, Naunehal S$$b18
000162869 7001_ $$00000-0002-8399-4009$$aLandeck, Natalie$$b19
000162869 7001_ $$00000-0002-6591-6269$$aLuk, Kelvin$$b20
000162869 7001_ $$00000-0003-0000-7096$$aMelki, Ronald$$b21
000162869 7001_ $$0P:(DE-2719)2810803$$aKahle, Philipp J$$b22$$udzne
000162869 7001_ $$00000-0002-2674-9891$$aHornemann, Simone$$b23
000162869 7001_ $$aKnowles, Tuomas P J$$b24
000162869 7001_ $$00000-0002-1058-3831$$aCookson, Mark R$$b25
000162869 7001_ $$aPolymenidou, Magdalini$$b26
000162869 7001_ $$0P:(DE-2719)2000010$$aJucker, Mathias$$b27$$udzne
000162869 7001_ $$00000-0002-0344-6708$$aAguzzi, Adriano$$b28
000162869 773__ $$0PERI:(DE-600)2485479-7$$a10.15252/emmm.202114745$$gVol. 13, no. 9$$n9$$pe14745$$tEMBO molecular medicine$$v13$$x1757-4684$$y2021
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