Insights into GBA Parkinson's disease pathology and therapy with induced pluripotent stem cell model systems

被引:13
作者
Baden, Pascale [1 ,2 ]
Yu, Cong [1 ,2 ]
Deleidi, Michela [1 ,2 ]
机构
[1] German Ctr Neurodegenerat Dis DZNE, D-72076 Tubingen, Germany
[2] Univ Tubingen, Hertie Inst Clin Brain Res, Ctr Neurol, D-72076 Tubingen, Germany
关键词
GBA; Parkinson's disease; Induced pluripotent stem cells; GAUCHER-DISEASE; ALPHA-SYNUCLEIN; GLUCOCEREBROSIDASE MUTATIONS; ENDOPLASMIC-RETICULUM; LYSOSOMAL STORAGE; MOUSE MODEL; MITOCHONDRIAL DYSFUNCTION; GLUCOSYLCERAMIDE LEVELS; BRAIN; RISK;
D O I
10.1016/j.nbd.2019.01.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
While the link between GBA and Parkinson's disease (PD) was initially unexpected, it is now well established that GBA mutations are the most frequent genetic risk for PD. GBA has also been linked to sporadic PD, dementia with Lewy bodies, and ageing. Thus, GBA represents a promising target to counteract brain disease and the age related decline of lysosomal function. The exact mechanisms involved in the risk of developing PD in GBA mutation carriers are still unclear and research in this field has faced the major challenge of a lack of proper modeling systems. Induced pluripotent stem cells (iPSCs) as well as advances in disease modeling and genome editing have facilitated studies of human brain disease. With regard to GBA-PD, iPSCs offer several advantages including the possibility of investigating sphingolipid (SPL) biology in relevant cells, the role of dopamine metabolism as well as non-cell autonomous mechanisms that are likely involved in the disease process. This review will summarize findings that emerged from iPSC-based studies in the context of GBA-PD pathology and therapy. We also highlight current advantages and challenges of stem cell models for neurological disease modeling and drug discovery.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 159 条
  • [1] Defects in trafficking bridge Parkinson's disease pathology and genetics
    Abeliovich, Asa
    Gitler, Aaron D.
    [J]. NATURE, 2016, 539 (7628) : 207 - 216
  • [2] The Complicated Relationship between Gaucher Disease and Parkinsonism: Insights from a Rare Disease
    Aflaki, Elma
    Westbroek, Wendy
    Sidransky, Ellen
    [J]. NEURON, 2017, 93 (04) : 737 - 746
  • [3] A New Glucocerebrosidase Chaperone Reduces α-Synuclein and Glycolipid Levels in iPSC-Derived Dopaminergic Neurons from Patients with Gaucher Disease and Parkinsonism
    Aflaki, Elma
    Borger, Daniel K.
    Moaven, Nima
    Stubblefield, Barbara K.
    Rogers, Steven A.
    Patnaik, Samarjit
    Schoenen, Frank J.
    Westbroek, Wendy
    Zheng, Wei
    Sullivan, Patricia
    Fujiwara, Hideji
    Sidhu, Rohini
    Khaliq, Zayd M.
    Lopez, Grisel J.
    Goldstein, David S.
    Ory, Daniel S.
    Marugan, Juan
    Sidransky, Ellen
    [J]. JOURNAL OF NEUROSCIENCE, 2016, 36 (28) : 7441 - 7452
  • [4] Lysosomal storage and impaired autophagy lead to inflammasome activation in Gaucher macrophages
    Aflaki, Elma
    Moaven, Nima
    Borger, Daniel K.
    Lopez, Grisel
    Westbroek, Wendy
    Chae, Jae Jin
    Marugan, Juan
    Patnaik, Samarjit
    Maniwang, Emerson
    Gonzalez, Ashley N.
    Sidransky, Ellen
    [J]. AGING CELL, 2016, 15 (01) : 77 - 88
  • [5] Macrophage Models of Gaucher Disease for Evaluating Disease Pathogenesis and Candidate Drugs
    Aflaki, Elma
    Stubblefield, Barbara K.
    Maniwang, Emerson
    Lopez, Grisel
    Moaven, Nima
    Goldin, Ehud
    Marugan, Juan
    Patnaik, Samarjit
    Dutra, Amalia
    Southall, Noel
    Zheng, Wei
    Tayebi, Nahid
    Sidransky, Ellen
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (240)
  • [6] Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations
    Alcalay, Roy N.
    Levy, Oren A.
    Waters, Cheryl C.
    Fahn, Stanley
    Ford, Blair
    Kuo, Sheng-Han
    Mazzoni, Pietro
    Pauciulo, Michael W.
    Nichols, William C.
    Gan-Or, Ziv
    Rouleau, Guy A.
    Chung, Wendy K.
    Wolf, Pavlina
    Oliva, Petra
    Keutzer, Joan
    Marder, Karen
    Zhang, Xiaokui
    [J]. BRAIN, 2015, 138 : 2648 - 2658
  • [7] Comparison of Parkinson Risk in Ashkenazi Jewish Patients With Gaucher Disease and GBA Heterozygotes
    Alcalay, Roy N.
    Dinur, Tama
    Quinn, Timothy
    Sakanaka, Karina
    Levy, Oren
    Waters, Cheryl
    Fahn, Stanley
    Dorovski, Tsvyatko
    Chung, Wendy K.
    Pauciulo, Michael
    Nichols, William
    Rana, Huma Q.
    Balwani, Manisha
    Bier, Louise
    Elstein, Deborah
    Zimran, Ari
    [J]. JAMA NEUROLOGY, 2014, 71 (06) : 752 - 757
  • [8] Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia
    Allison, Rachel
    Edgar, James R.
    Pearson, Guy
    Rizo, Tania
    Newton, Timothy
    Guenther, Sven
    Berner, Fiamma
    Hague, Jennifer
    Connell, James W.
    Winkler, Juergen
    Lippincott-Schwartz, Jennifer
    Beetz, Christian
    Winner, Beate
    Reid, Evan
    [J]. JOURNAL OF CELL BIOLOGY, 2017, 216 (05) : 1337 - 1355
  • [9] Altered TFEB-mediated lysosomal biogenesis in Gaucher disease iPSC-derived neuronal cells
    Awad, Ola
    Sarkar, Chinmoy
    Panicker, Leelamma M.
    Miller, Diana
    Zeng, Xianmin
    Sgambato, Judi A.
    Lipinski, Marta M.
    Feldman, Ricardo A.
    [J]. HUMAN MOLECULAR GENETICS, 2015, 24 (20) : 5775 - 5788
  • [10] Glucocerebrosidase and Parkinson Disease: Molecular, Clinical, and Therapeutic Implications
    Balestrino, Roberta
    Schapira, Anthony H. V.
    [J]. NEUROSCIENTIST, 2018, 24 (05) : 540 - 559