Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease

Parkinson’s disease (PD) is a well-known age-related neurodegenerative disease. Considering the vital importance of disease modeling based on reprogramming technology, we adopted direct reprogramming to human-induced neuronal progenitor cells (hiNPCs) for in vitro assessment of potential therapeutic...

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Main Authors: Joo-Eun Lee, Hyuna Sim, Hee Min Yoo, Minhyung Lee, Aruem Baek, Young-Joo Jeon, Kang-Sik Seo, Mi-Young Son, Joo Seog Yoon, Janghwan Kim
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/25/16/3602
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author Joo-Eun Lee
Hyuna Sim
Hee Min Yoo
Minhyung Lee
Aruem Baek
Young-Joo Jeon
Kang-Sik Seo
Mi-Young Son
Joo Seog Yoon
Janghwan Kim
author_facet Joo-Eun Lee
Hyuna Sim
Hee Min Yoo
Minhyung Lee
Aruem Baek
Young-Joo Jeon
Kang-Sik Seo
Mi-Young Son
Joo Seog Yoon
Janghwan Kim
author_sort Joo-Eun Lee
collection DOAJ
description Parkinson’s disease (PD) is a well-known age-related neurodegenerative disease. Considering the vital importance of disease modeling based on reprogramming technology, we adopted direct reprogramming to human-induced neuronal progenitor cells (hiNPCs) for in vitro assessment of potential therapeutics. In this study, we investigated the neuroprotective effects of cryptotanshinone (CTN), which has been reported to have antioxidant properties, through PD patient-derived hiNPCs (PD-iNPCs) model with induced oxidative stress and cell death by the proteasome inhibitor MG132. A cytotoxicity assay showed that CTN possesses anti-apoptotic properties in PD-hiNPCs. CTN treatment significantly reduced cellular apoptosis through mitochondrial restoration, such as the reduction in mitochondrial reactive oxygen species and increments of mitochondrial membrane potential. These effects of CTN are mediated via the nuclear factor erythroid 2-related factor 2 (NRF2) pathway in PD-hiNPCs. Consequently, CTN could be a potential antioxidant reagent for preventing disease-related pathological phenotypes of PD.
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spelling doaj.art-b33d6504793c43b1a52339a90eeb14332023-11-20T09:28:13ZengMDPI AGMolecules1420-30492020-08-012516360210.3390/molecules25163602Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s DiseaseJoo-Eun Lee0Hyuna Sim1Hee Min Yoo2Minhyung Lee3Aruem Baek4Young-Joo Jeon5Kang-Sik Seo6Mi-Young Son7Joo Seog Yoon8Janghwan Kim9Stem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaStem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaGroup for Biometrology, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, KoreaStem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaStem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaStem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaHuen Co., Ltd., Gwanggyo Business Center 5F (#508), 156, Gwanggyo-ro, Yeongtong-gu, Suwon 16506, KoreaStem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaHuen Co., Ltd., Gwanggyo Business Center 5F (#508), 156, Gwanggyo-ro, Yeongtong-gu, Suwon 16506, KoreaStem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaParkinson’s disease (PD) is a well-known age-related neurodegenerative disease. Considering the vital importance of disease modeling based on reprogramming technology, we adopted direct reprogramming to human-induced neuronal progenitor cells (hiNPCs) for in vitro assessment of potential therapeutics. In this study, we investigated the neuroprotective effects of cryptotanshinone (CTN), which has been reported to have antioxidant properties, through PD patient-derived hiNPCs (PD-iNPCs) model with induced oxidative stress and cell death by the proteasome inhibitor MG132. A cytotoxicity assay showed that CTN possesses anti-apoptotic properties in PD-hiNPCs. CTN treatment significantly reduced cellular apoptosis through mitochondrial restoration, such as the reduction in mitochondrial reactive oxygen species and increments of mitochondrial membrane potential. These effects of CTN are mediated via the nuclear factor erythroid 2-related factor 2 (NRF2) pathway in PD-hiNPCs. Consequently, CTN could be a potential antioxidant reagent for preventing disease-related pathological phenotypes of PD.https://www.mdpi.com/1420-3049/25/16/3602Parkinson’s diseasecryptotanshinonedisease modelingmitochondrial dysfunctionantioxidant
spellingShingle Joo-Eun Lee
Hyuna Sim
Hee Min Yoo
Minhyung Lee
Aruem Baek
Young-Joo Jeon
Kang-Sik Seo
Mi-Young Son
Joo Seog Yoon
Janghwan Kim
Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease
Molecules
Parkinson’s disease
cryptotanshinone
disease modeling
mitochondrial dysfunction
antioxidant
title Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease
title_full Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease
title_fullStr Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease
title_full_unstemmed Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease
title_short Neuroprotective Effects of Cryptotanshinone in a Direct Reprogramming Model of Parkinson’s Disease
title_sort neuroprotective effects of cryptotanshinone in a direct reprogramming model of parkinson s disease
topic Parkinson’s disease
cryptotanshinone
disease modeling
mitochondrial dysfunction
antioxidant
url https://www.mdpi.com/1420-3049/25/16/3602
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