A microfluidic-based neurotoxin concentration gradient for the generation of an in vitro model of Parkinson's disease

被引:49
作者
Seidi, Azadeh [1 ]
Kaji, Hirokazu [2 ,3 ,4 ]
Annabi, Nasim [5 ]
Ostrovidov, Serge [1 ]
Ramalingam, Murugan [1 ,6 ]
Khademhosseini, Ali [1 ,2 ,3 ,7 ]
机构
[1] Tohoku Univ, WPI Adv Inst Mat Res, Sendai, Miyagi 9808577, Japan
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Ctr Biomed Engn, Cambridge, MA 02139 USA
[3] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[4] Tohoku Univ, Dept Bioengn & Robot, Grad Sch Engn, Sendai, Miyagi 9808579, Japan
[5] Univ Sydney, Sch Chem & Biomol Engn, Sydney, NSW 2006, Australia
[6] Univ Strasbourg, Fac Med, Natl Inst Hlth & Med Res U977, F-67085 Strasbourg, France
[7] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
关键词
6-HYDROXYDOPAMINE-INDUCED APOPTOSIS; CYSTEINE PROTEASE; CYTOTOXICITY; INVOLVEMENT; ACTIVATION; NEURONS; CELLS;
D O I
10.1063/1.3580756
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
In this study, we developed a miniaturized microfluidic-based high-throughput cell toxicity assay to create an in vitro model of Parkinson's disease (PD). In particular, we generated concentration gradients of 6-hydroxydopamine (6-OHDA) to trigger a process of neuronal apoptosis in pheochromocytoma PC12 neuronal cell line. PC12 cells were cultured in a microfluidic channel, and a concentration gradient of 6-OHDA was generated in the channel by using a back and forth movement of the fluid flow. Cellular apoptosis was then analyzed along the channel. The results indicate that at low concentrations of 6-OHDA along the gradient (i.e., approximately less than 260 mu M), the neuronal death in the channel was mainly induced by apoptosis, while at higher concentrations, 6-OHDA induced neuronal death mainly through necrosis. Thus, this concentration appears to be useful for creating an in vitro model of PD by inducing the highest level of apoptosis in PC12 cells. As microfluidic systems are advantageous in a range of properties such as throughput and lower use of reagents, they may provide a useful approach for generating in vitro models of disease for drug discovery applications. (C) 2011 American Institute of Physics. [doi:10.1063/1.3580756]
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页数:14
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