Parkinson’s disease phenotypes in patient neuronal cultures and brain organoids improved by 2-Hydroxypropyl-b-Cyclodextrin treatmentJarazo, Javier ; Barmpa, Kyriaki ; et alin Movement Disorders (2021) Detailed reference viewed: 224 (25 UL) The Parkinson’s-disease-associated mutation LRRK2-G2019S alters dopaminergic differentiation dynamics via NR2F1; Bolognin, Silvia ; et alin Cell Reports (2021) Detailed reference viewed: 180 (11 UL) Neural Stem Cells of Parkinson's Disease Patients Exhibit Aberrant Mitochondrial Morphology and Functionality; Bolognin, Silvia ; Antony, Paul et alin Stem Cell Reports (2019) Detailed reference viewed: 393 (37 UL) Modeling Parkinson’s disease in midbrain-like organoidsSmits, Lisa ; ; et alin NPJ Parkinson's Disease (2019) Detailed reference viewed: 370 (24 UL) Impaired serine metabolism complements LRRK2-G2019S pathogenicity in PD patientsNickels, Sarah ; ; Bolognin, Silvia et alin Parkinsonism and Related Disorders (2019) Detailed reference viewed: 333 (43 UL) Guidelines for Fluorescent Guided Biallelic HDR Targeting Selection With PiggyBac System Removal for Gene EditingJarazo, Javier ; ; Schwamborn, Jens Christian ![]() in Frontiers in Genetics (2019) Detailed reference viewed: 260 (9 UL) 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug TestingBolognin, Silvia ; ; et alin Advanced Science (2018) Parkinson's disease (PD)‐specific neurons, grown in standard 2D cultures, typically only display weak endophenotypes. The cultivation of PD patient‐specific neurons, derived from induced pluripotent stem ... [more ▼] Parkinson's disease (PD)‐specific neurons, grown in standard 2D cultures, typically only display weak endophenotypes. The cultivation of PD patient‐specific neurons, derived from induced pluripotent stem cells carrying the LRRK2‐G2019S mutation, is optimized in 3D microfluidics. The automated image analysis algorithms are implemented to enable pharmacophenomics in disease‐relevant conditions. In contrast to 2D cultures, this 3D approach reveals robust endophenotypes. High‐content imaging data show decreased dopaminergic differentiation and branching complexity, altered mitochondrial morphology, and increased cell death in LRRK2‐G2019S neurons compared to isogenic lines without using stressor agents. Treatment with the LRRK2 inhibitor 2 (Inh2) rescues LRRK2‐G2019S‐dependent dopaminergic phenotypes. Strikingly, a holistic analysis of all studied features shows that the genetic background of the PD patients, and not the LRRK2‐G2019S mutation, constitutes the strongest contribution to the phenotypes. These data support the use of advanced in vitro models for future patient stratification and personalized drug development. [less ▲] Detailed reference viewed: 453 (42 UL) CRISPR/Cas9 and piggyBac-mediated footprint-free LRRK2-G2019S knock-in reveals neuronal complexity phenotypes and α-Synuclein modulation in dopaminergic neurons; Walter, Jonas ; Jarazo, Javier et alin Stem Cell Research (2017) Detailed reference viewed: 347 (7 UL) |
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