Hepatotoxicity of copper sulfide nanoparticles towards hepatocyte spheroids using a novel multi-concave agarose chip method

Author:

Jiang Tianyan1,Guo Haoxiang1,Xia Ya-Nan1,Liu Yun23,Chen Dandan1,Pang Guibin4,Feng Yahui5,Yu Huan1,Wu Yanxian1,Zhang Shaodian6,Wang Yangyun1,Wang Yong1,Wen Hairuo7,Zhang Leshuai W1

Affiliation:

1. School of Radiation Medicine & Protection, State Key Laboratory of Radiation Medicine & Protection, School for Radiological & Interdisciplinary Sciences (RAD-X), Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, 215123, PR China

2. Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, PR China

3. Shanghai R&D Centre for Standardization of Chinese Medicines, Shanghai, 201210, PR China

4. State Key Laboratory of Bioreactor Engineering, East China University of Science & Technology, Shanghai, PR China

5. Department of Science & Technology, The Second Affiliated Hospital of Chengdu Medical College, China National Nuclear Corporation 416 Hospital, Chengdu, 610051, PR China

6. The Second Affiliated Hospital of Soochow University, 1055 Sanxiang Road, Suzhou, 215004, PR China

7. Beijing Key Laboratory, National Center for Safety Evaluation of Drugs, National Institutes for Food & Drug Control, Beijing, 100176, PR China

Abstract

Aim: To explore the hepatotoxicity of copper sulfide nanoparticles (CuSNPs) toward hepatocyte spheroids. Materials & methods: Other than the traditional agarose method to generate hepatocyte spheroids, we developed a multi-concave agarose chip (MCAC) method to investigate changes in hepatocyte viability, morphology, mitochondrial membrane potential, reactive oxygen species and hepatobiliary transporter by CuSNPs. Results: The MCAC method allowed a large number of spheroids to be obtained per sample. CuSNPs showed hepatotoxicity in vitro through a decrease in spheroid viability, albumin/urea production and glycogen deposition. CuSNPs also introduced hepatocyte spheroid injury through alteration of mitochondrial membrane potential and reactive oxygen species, that could be reversed by N-acetyl-l-cysteine. CuSNPs significantly decreased the activity of BSEP transporter by downregulating its mRNA and protein levels. Activity of the MRP2 transporter remained unchanged. Conclusion: We observed the hepatotoxicity of CuSNPs in vitro with associated mechanisms in an advanced 3D culture system.

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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