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Nat Commun ; 9(1): 4815, 2018 11 16.
Artigo em Inglês | MEDLINE | ID: mdl-30446643

RESUMO

Common disorders, including diabetes and Parkinson's disease, are caused by a combination of environmental factors and genetic susceptibility. However, defining the mechanisms underlying gene-environment interactions has been challenging due to the lack of a suitable experimental platform. Using pancreatic ß-like cells derived from human pluripotent stem cells (hPSCs), we discovered that a commonly used pesticide, propargite, induces pancreatic ß-cell death, a pathological hallmark of diabetes. Screening a panel of diverse hPSC-derived cell types we extended this observation to a similar susceptibility in midbrain dopamine neurons, a cell type affected in Parkinson's disease. We assessed gene-environment interactions using isogenic hPSC lines for genetic variants associated with diabetes and Parkinson's disease. We found GSTT1-/- pancreatic ß-like cells and dopamine neurons were both hypersensitive to propargite-induced cell death. Our study identifies an environmental chemical that contributes to human ß-cell and dopamine neuron loss and validates a novel hPSC-based platform for determining gene-environment interactions.


Assuntos
Cicloexanos/toxicidade , Diabetes Mellitus/induzido quimicamente , Neurônios Dopaminérgicos/efeitos dos fármacos , Interação Gene-Ambiente , Células Secretoras de Insulina/efeitos dos fármacos , Praguicidas/toxicidade , Animais , Morte Celular/efeitos dos fármacos , Morte Celular/genética , Diferenciação Celular , Diabetes Mellitus/genética , Diabetes Mellitus/patologia , Neurônios Dopaminérgicos/citologia , Neurônios Dopaminérgicos/enzimologia , Glutationa Transferase/deficiência , Glutationa Transferase/genética , Humanos , Células Secretoras de Insulina/citologia , Células Secretoras de Insulina/enzimologia , Mesencéfalo/citologia , Mesencéfalo/efeitos dos fármacos , Mesencéfalo/enzimologia , Camundongos , Modelos Biológicos , Doença de Parkinson/etiologia , Doença de Parkinson/genética , Doença de Parkinson/patologia , Células-Tronco Pluripotentes/citologia , Células-Tronco Pluripotentes/enzimologia
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