LRRK2 kinase inhibition reverses G2019S mutation-dependent effects on tau pathology progression  

作　　者：Noah Lubben Julia K.Brynildsen Connor M.Webb Howard L.Li Cheryl E.G.Leyns Lakshmi Changolkar Bin Zhang Emily S.Meymand Mia O’Reilly Zach Madaj Daniella DeWeerd Matthew J.Fell Virginia M.Y.Lee Dani S.Bassett Michael X.Henderson 

机构地区：[1]Department of Neurodegenerative Science,Van Andel Institute,333 Bostwick Ave NE,Grand Rapids,MI 49503,USA [2]Aligning Science Across Parkinson’s(ASAP)Collaborative Research Network,Chevy Chase,MD 20815,USA [3]Department of Bioengineering,University of Pennsylvania,Philadelphia,PA 19104,USA [4]Department of Pathology and Laboratory Medicine,Perelman School of Medicine,Institute On Aging and Center for Neurodegenerative Disease Research,University of Pennsylvania,Philadelphia,PA 19104,USA [5]Neu-roscience Discovery,Merck&Co.,Inc.,Boston,MA 02115,USA [6]Department of Electrical and Systems Engineering,University of Pennsylvania,Philadelphia,PA 19104,USA [7]Department of Physics and Astronomy,University of Penn-sylvania,Philadelphia,PA 19104,USA [8]Department of Neurology,University of Pennsylvania,Philadelphia,PA 19104,USA [9]Department of Psychiatry,University of Pennsylvania,Philadelphia,PA 19104,USA [10]Santa Fe Institute,Santa Fe,NM 87501,USA [11]Bioinformatics and Biostatistics Core,Van Andel Institute,333 Bostwick Ave.,NE,Grand Rapids,MI 49503,USA

出　　处：《Translational Neurodegeneration》2024年第1期884-903,共20页转化神经变性病(英文)

基　　金：supported by the Michael J.Fox Foundation for Parkinson’s Research(MJFF)grant 16879(M.X.H)and Aligning Science Across Parkinson’s ASAP-020616 through MJFF;NIH grants:R01-AG077573(D.S.B,M.X.H.);NSF grants PHY-1554488(D.S.B)and BCS-1631550(D.S.B).D.S.B.also acknowledges support from the John D.and Catherine T.MacArthur Foundation,the ISI Foundation,the Alfred P.Sloan Foundation,and the Paul G.Allen Foundation.

摘　　要：Background Mutations in leucine-rich repeat kinase 2(LRRK2)are the most common cause of familial Parkinson’s disease(PD).These mutations elevate the LRRK2 kinase activity,making LRRK2 kinase inhibitors an attractive therapeutic.LRRK2 kinase activity has been consistently linked to specific cell signaling pathways,mostly related to organelle trafficking and homeostasis,but its relationship to PD pathogenesis has been more difficult to define.LRRK2-PD patients consistently present with loss of dopaminergic neurons in the substantia nigra but show variable development of Lewy body or tau tangle pathology.Animal models carrying LRRK2 mutations do not develop robust PD-related phenotypes spontaneously,hampering the assessment of the efficacy of LRRK2 inhibitors against disease processes.We hypothesized that mutations in LRRK2 may not be directly related to a single disease pathway,but instead may elevate the susceptibility to multiple disease processes,depending on the disease trigger.To test this hypothesis,we have previously evaluated progression ofα-synuclein and tau pathologies following injection of proteopathic seeds.We demonstrated that transgenic mice overexpressing mutant LRRK2 show alterations in the brain-wide progression of pathology,especially at older ages.Methods Here,we assess tau pathology progression in relation to long-term LRRK2 kinase inhibition.Wild-type or LRRK2^(G2019S) knock-in mice were injected with tau fibrils and treated with control diet or diet containing LRRK2 kinase inhibitor MLi-2 targeting the IC50 or IC90 of LRRK2 for 3-6 months.Mice were evaluated for tau pathology by brain-wide quantitative pathology in 844 brain regions and subsequent linear diffusion modeling of progression.Results Consistent with our previous work,we found systemic alterations in the progression of tau pathology in LRRK2^(G2019S) mice,which were most pronounced at 6 months.Importantly,LRRK2 kinase inhibition reversed these effects in LRRK2^(G2019S) mice,but had minimal effect in wild-type mice,suggesting tha

关 键 词：G2019S MLi-2 Cell-to-cell spread Transmission Genetic risk MAPT 

分 类 号：R73[医药卫生—肿瘤]