The Effect of glna Loss on the Physiological and Pathological Phenotype of Parkinson's Disease C. elegans

被引:0
作者
Liang, Qifei [1 ,2 ]
Zhao, Guangrong [1 ]
机构
[1] Tongji Univ, Sch Med, Shanghai, Peoples R China
[2] Nanjing Drum Tower Hosp, Nanjing, Peoples R China
关键词
C; elegans; dopaminergic neurons; glna; PD; CAENORHABDITIS-ELEGANS; DOPAMINERGIC-NEURONS; MODEL; STRESS;
D O I
10.1002/jcla.25129
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BackgroundParkinson's disease (PD) is a common neurodegenerative disease. Glutamate(Glu) excitotoxicity is one of the main pathogenesis of PD. Glutaminase (Gls) is an enzyme primarily responsible for catalyzing the hydrolysis and deamidation of glutamine (Gln) to produce Glu and ammonia. Inhibiting the function of Gls may have a beneficial effect on the treatment of PD by reducing the production of Glu. The homologous gene of Gls in C. elegans is glna.AimsTo explore the effects of glna loss on physiological and pathological phenotype of PD C. elegans, and to provide new ideas and references for the research and treatment of PD.Materials & MethodsWe used PD C. elegans UA44 and QIN27 to detect development and lifespan, behavior, degeneration of dopaminergic neurons, lipid levels, ROS levels, expression levels of common amino acids.ResultsGlna loss had no significant impact on the development and lifespan of PD C. elegans. Glna loss saved part of the decline of motor function, including the head thrash frequency and the body bend frequency, and the difference was significant. There was a trend of improvement in some motor behaviors, such as the ethanol avoidance experiment, while no improvement was observed in other experiments. Glna loss slowed down the degeneration of dopaminergic neurons. Glna loss increased the lipid levels and ROS levels in C. elegans. Glna loss decreased Glu content and increased Gln content in C. elegans.DiscussionThe effect of glna loss on PD C. elegans may be the result of multiple factors, such as the tissue types of alpha-syn expression in C. elegans, the PD C. elegans model used, the adverse effects of glna loss on other systems, and the changes in ROS levels in C. elegans. The specific mechanisms causing these phenomena are still unclear and need to be further explored.ConclusionGlna loss has a certain protective effect on dopaminergic neurons in PD C. elegans, while the improvement effect on movement and behavior is limited.
引用
收藏
页数:15
相关论文
共 46 条
  • [1] Lipid peroxidation is essential for α-synuclein-induced cell death
    Angelova, Plamena R.
    Horrocks, Mathew H.
    Klenerman, David
    Gandhi, Sonia
    Abramov, Andrey Y.
    Shchepinov, Mikhail S.
    [J]. JOURNAL OF NEUROCHEMISTRY, 2015, 133 (04) : 582 - 589
  • [2] BRENNER S, 1974, GENETICS, V77, P71
  • [3] Modeling neurodegeneration in Caenorhabditis elegans
    Caldwell, Kim A.
    Willicott, Corey W.
    Caldwell, Guy A.
    [J]. DISEASE MODELS & MECHANISMS, 2020, 13 (10)
  • [4] Torsin-mediated protection from cellular stress in the dopaminergic neurons of Caenorhabditis elegans
    Cao, SS
    Gelwix, CC
    Caldwell, KA
    Caldwell, GA
    [J]. JOURNAL OF NEUROSCIENCE, 2005, 25 (15) : 3801 - 3812
  • [5] Neurotoxicity of nonylphenol exposure on Caenorhabditis elegans induced by reactive oxidative species and disturbance synthesis of serotonin
    Cao, Xue
    Wang, Xiaoli
    Chen, Haibo
    Li, Hui
    Tariq, Muhammad
    Wang, Chen
    Zhou, Yuanyuan
    Liu, Yongdi
    [J]. ENVIRONMENTAL POLLUTION, 2019, 244 : 947 - 957
  • [6] Oxidative Stress Mechanisms Underlying Parkinson's Disease-Associated Neurodegeneration in C. elegans
    Chakraborty, Sudipta
    Bornhorst, Julia
    Nguyen, Thuy T.
    Aschner, Michael
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (11): : 23103 - 23128
  • [7] Diterpene glycosides from Holothuria scabra exert the α-synuclein degradation and neuroprotection against α-synuclein-Mediated neurodegeneration in C. elegans model
    Chalorak, Pawanrat
    Sornkaew, Nilubon
    Manohong, Preeyanuch
    Niamnont, Nakorn
    Malaiwong, Nawaphat
    Limboonreung, Tanapol
    Sobhon, Prasert
    Aschner, Michael
    Meemon, Krai
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2021, 279
  • [8] Accelerated in vitro fibril formation by a mutant α-synuclein linked to early-onset Parkinson disease
    Conway, KA
    Harper, JD
    Lansbury, PT
    [J]. NATURE MEDICINE, 1998, 4 (11) : 1318 - 1320
  • [9] Whole-animal connectomes of both Caenorhabditis elegans sexes
    Cook, Steven J.
    Jarrell, Travis A.
    Brittin, Christopher A.
    Wang, Yi
    Bloniarz, Adam E.
    Yakovlev, Maksim A.
    Nguyen, Ken C. Q.
    Tang, Leo T. -H.
    Bayer, Emily A.
    Duerr, Janet S.
    Bulow, Hannes E.
    Hobert, Oliver
    Hall, David H.
    Emmons, Scott W.
    [J]. NATURE, 2019, 571 (7763) : 63 - +
  • [10] GLS1 Mutant Mice Display Moderate Alterations of Hippocampal Glutamatergic Neurotransmission Associated with Specific Adaptive Behavioral Changes
    Dutar, Patrick
    Tolle, Virginie
    Kervern, Myriam
    Carcenac, Carole
    Carola, Valeria
    Gross, Cornelius
    Savasta, Marc
    Darmon, Michele
    Masson, Justine
    [J]. NEUROSCIENCE, 2019, 396 : 175 - 186