Rossignoli, G;
Krämer, K;
Lugarà, E;
Alrashidi, H;
Pope, S;
De La Fuente Barrigon, C;
Barwick, K;
... Kurian, MA; + view all
(2021)
Aromatic L-amino acid decarboxylase deficiency: a patient-derived neuronal model for precision therapies.
Brain
10.1093/brain/awab123.
(In press).
Preview |
Text
Counsell_Aromatic l-amino acid decarboxylase deficiency- a patient-derived neuronal model for precision therapies_AAM.pdf - Accepted Version Download (3MB) | Preview |
Abstract
Aromatic L-amino acid decarboxylase (AADC) deficiency is a complex inherited neurological disorder of monoamine synthesis which results in dopamine and serotonin deficiency. The majority of affected individuals have variable, though often severe cognitive and motor delay, with a complex movement disorder and high risk of premature mortality. For most, standard pharmacological treatment provides only limited clinical benefit. Promising gene therapy approaches are emerging, though may not be either suitable or easily accessible for all patients. In order to better characterize the underlying disease pathophysiology and guide precision therapies, we generated a patient-derived midbrain dopaminergic (mDA) neuronal model of AADC deficiency from induced pluripotent stem cells (iPSCs). The neuronal model recapitulates key disease features, including absent AADC enzyme activity and dysregulated dopamine metabolism. We observed developmental defects affecting synaptic maturation and neuronal electrical properties, which were improved by lentiviral gene therapy. Bioinformatic and biochemical analyses on recombinant AADC predicted that the activity of one variant could be improved by L-3,4-dihydroxyphenylalanine (L-DOPA) administration; this hypothesis was corroborated in the patient-derived neuronal model, where L-DOPA treatment leads to amelioration of dopamine metabolites. Our study has shown that patient-derived disease modelling provides further insight into the neurodevelopmental sequelae of AADC deficiency, as well as a robust platform to investigate and develop personalised therapeutic approaches.
Archive Staff Only
 |
View Item |
