Initial phase establishment of an in vitro method for developmental neurotoxicity test using Ki-67 in human neural progenitor cells.

IF 2 4区 医学 Q3 PHYSIOLOGY Journal of Physiology and Pharmacology Pub Date : 2023-04-01 DOI:10.26402/jpp.2023.2.07
S M Go, B Lee, C Ahn, S H Jeong, N R Jo, S M Park, M Lee, D N Tran, E-M Jung, S D Lee, E-B Jeung
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Abstract

Building a precise alternative neurotoxicological test is of great importance to respond to societal and ethical requirements. In this study, a new developmental neurotoxicity test (DNT) was established with the human neural progenitor cell line. ReNcell CX cells were exposed to neurotoxic chemicals (aphidicolin, hydroxyurea, cytosine arabinoside, 5-fluorouracil, and ochratoxin A) or non-neurotoxic chemicals (sodium gluconate, sodium bicarbonate, penicillin G, and saccharin). Propidium iodide (PI) was used to evaluate cell viability. BrdU and Ki-76 were employed to determine cell proliferation. Based on the cell viability and proliferation, mathematical models were built by linear discriminant analysis. Furthermore, the neurotoxic-considered chemicals inhibited cell cycle progression at the protein level, supporting the biomolecular rationale for the predictive model. Overall, these results show that the new test method can be used to determine the potential developmental neurotoxicants or new drug candidates.

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用Ki-67对人神经祖细胞进行发育性神经毒性体外试验的初步建立。
建立一种精确的替代神经毒理学测试对于响应社会和伦理要求具有重要意义。在本研究中,建立了一种新的发育性神经毒性试验(DNT)。ReNcell CX细胞暴露于神经毒性化学物质(阿菲霉素、羟基脲、阿拉伯糖胞嘧啶、5-氟尿嘧啶和赭曲霉毒素A)或非神经毒性化学物质(葡萄糖酸钠、碳酸氢钠、青霉素G和糖精)。用碘化丙啶(PI)评价细胞活力。BrdU和Ki-76检测细胞增殖。根据细胞活力和增殖情况,通过线性判别分析建立数学模型。此外,神经毒性化学物质在蛋白质水平上抑制细胞周期进程,支持预测模型的生物分子理论基础。总之,这些结果表明,新的测试方法可用于确定潜在的发育神经毒物或新的候选药物。
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CiteScore
4.00
自引率
22.70%
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0
审稿时长
6-12 weeks
期刊介绍: Journal of Physiology and Pharmacology publishes papers which fall within the range of basic and applied physiology, pathophysiology and pharmacology. The papers should illustrate new physiological or pharmacological mechanisms at the level of the cell membrane, single cells, tissues or organs. Clinical studies, that are of fundamental importance and have a direct bearing on the pathophysiology will also be considered. Letters related to articles published in The Journal with topics of general professional interest are welcome.
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