A multichannel microfluidic device for revealing the neurotoxic effects of Bisphenol S on cerebral organoids under low-dose constant exposure

被引:0
|
作者
Abdulla, Aynur [1 ,2 ,3 ]
Yan, Haoni [1 ,2 ]
Chen, Shujin [6 ]
Wu, Leqi [3 ]
Chen, Xu-Sen [3 ]
Zhang, Yizhi [3 ]
Zhang, Manlin [3 ]
Zhuang, Tsz Yui [3 ]
Ahmad, Khan Zara [4 ]
Lin, Jinjin [3 ,5 ]
Ding, Xianting [1 ,2 ,3 ]
Jiang, Lai [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Dept Anesthesiol & Surg Intens Care Unit, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai 200092, Peoples R China
[3] Shanghai Jiao Tong Univ, Inst Personalized Med, Sch Biomed Engn, State Key Lab Oncogenes & Related Genes, Shanghai 200030, Peoples R China
[4] Karolinska Inst, Dept Lab Med, Div Pathol, Huddinge, Sweden
[5] Shaanxi Normal Univ, Sch Psychol, Xian 710062, Shaanxi, Peoples R China
[6] Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Shanghai Key Lab Childrens Environm Hlth,Minist Ed, Shanghai 200092, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2025年 / 267卷
基金
中国国家自然科学基金;
关键词
Microfluidic chip; Cerebral organoids; Bisphenol S; Neurotoxicity; DIFFERENTIATION; GENERATION; LHX5;
D O I
10.1016/j.bios.2024.116754
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Bisphenol S is a widely used plasticizer in manufacturing daily supplies, while little was known about its adverse effect on human health, especially on fetal brain development. Due to the complexity and subtlety of the brain, it remains challenging to reveal the hazardous effects of environmental pollution on human fetal brain development. Taking advantage of stem cell application, cerebral organoids generated from stem cells are becoming powerful tools for understanding brain development and drug toxicity testing models. Here, we developed a microfluidic chip for cerebral organoid culturing to reveal the neurotoxicity of low-dose constant BPS exposure on cerebral organoids. The organoids in our microfluidic system could be continuously cultured for 34 days and expressed all the essential properties of the cerebral organoids. Exposure to BPS was initiated from day 20 for concessive two weeks. The neurotoxic effects were evaluated by immunofluorescence staining and proteomics, and verified by quantitative real-time PCR. Our results indicated BPS exposure would inhibit neuron differentiation, hinder the Wnt signaling pathway, and cause alteration of signaling molecule expressions in brain regionalization. Even exposure to a low dose of BPS constantly might cause neurotoxicity during fetal brain development. Altogether, the multichannel microfluidic chip offers a general platform technique to reveal the effects of different hazardous chemicals on cerebral organoids.
引用
收藏
页数:10
相关论文
共 24 条
  • [21] Developmental low-dose exposure to bisphenol A results in gender-specific and non-monotonic effects on Fischer F344 rat bone
    Lejonklou, M. Halin
    Lind, T.
    Rasmusson, A.
    Larsson, S.
    Melhus, H.
    Lind, P. M.
    TOXICOLOGY LETTERS, 2015, 238 (02) : S255 - S255
  • [22] Subchronic Low-Dose Methylmercury Exposure Accelerated Cerebral Telomere Shortening in Relevant with Declined Urinary aMT6s Level in Rats
    Wu, Xi
    Li, Ping
    Tao, Junyan
    Chen, Xiong
    Zhang, Aihua
    TOXICS, 2023, 11 (02)
  • [23] Genome-wide gene expression profiling of low-dose, long-term exposure of human osteosarcoma cells to bisphenol A and its analogs bisphenols AF and S
    Fic, A.
    Mlakar, S. Jurkovic
    Juvan, P.
    Mlakar, V.
    Marc, J.
    Dolenc, M. Sollner
    Broberg, K.
    Masic, L. Peterlin
    TOXICOLOGY IN VITRO, 2015, 29 (05) : 1060 - 1069
  • [24] Rapid Responses and Mechanism of Action for Low-Dose Bisphenol S on ex Vivo Rat Hearts and Isolated Myocytes: Evidence of Female-Specific Proarrhythmic Effects
    Gao, Xiaoqian
    Ma, Jianyong
    Chen, Yamei
    Wang, Hong-Sheng
    ENVIRONMENTAL HEALTH PERSPECTIVES, 2015, 123 (06) : 571 - 578