Identification of the differential and synergic lipotoxic patterns of oleic acid, palmitic acid, and their mixture in 3D HepG2/C3A tissue using liver-on-chip technology

IF 2.8 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Biotechnology Progress Pub Date : 2026-02-16 Epub Date: 2025-10-13 DOI:10.1002/btpr.70075
Lisa Morisseau, Valérie Pawlowski, Valérie Plaisance, Mathilde Lucas, Cécile Legallais, Yasuyuki Sakai, Amar Abderrahmani, Rachid Jellali, Eric Leclerc
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引用次数: 0

Abstract

The metabolic dysfunction-associated steatotic liver disease (MASLD, previously formerly known as non-alcoholic fatty liver disease, NAFLD) is rapidly expanding worldwide in parrallel with the obesity pandemic. Dietary fatty acids including oleic (OA) and palmitic acids (PA) contribute to the hepatic intracellular triglyceride accumulation, and are therefore thought to play key roles in disease development and progression. Taking advantage of the cutting-edge organ-on-chip technology that mimics the 3D organ dynamic environment, we aimed at investigating the role of OA, PA and a 2:1 OA/PA mixture on the growth and function of the HepG2/C3A, a liver cell line model, over 2 and 7 days. OA supported sustained cell growth, leading to dense 3D tissues, whereas PA and OA exposure did not affect cell proliferation. PA treatment downregulated the GLUT2, INSRA, SREBP1, FASN, mRNA levels indicating a lipid metabolism perturbation in our model. The cell dysfunction caused by OA, PA, and OA/PA was associated with an increase in reactive oxygen species (ROS) production over time. Intracellular lipid monitored by oil red O was higher in cells exposed to OA than in the control ones and cells cultured with PA. Our data confirm the role of fatty acids on the growth and dysfunction of HepG2/C3A cells, and highlight distinct mechanisms through which OA and PA exert their effects.

利用肝脏芯片技术鉴定油酸、棕榈酸及其混合物在三维HepG2/C3A组织中的差异和协同脂毒模式。
代谢功能障碍相关的脂肪变性肝病(MASLD,以前称为非酒精性脂肪性肝病,NAFLD)在全球范围内与肥胖流行同步迅速扩大。包括油酸(OA)和棕榈酸(PA)在内的膳食脂肪酸有助于肝细胞内甘油三酯的积累,因此被认为在疾病的发生和进展中起关键作用。利用尖端的器官芯片技术,模拟三维器官动态环境,我们旨在研究OA, PA和2:1 OA/PA混合物对HepG2/C3A(肝细胞系模型)生长和功能的作用,为期2天和7天。OA支持细胞持续生长,导致致密的3D组织,而PA和OA暴露不影响细胞增殖。在我们的模型中,PA处理下调了GLUT2, INSRA, SREBP1, FASN mRNA水平,表明脂质代谢紊乱。随着时间的推移,OA、PA和OA/PA引起的细胞功能障碍与活性氧(ROS)产生的增加有关。在暴露于OA的细胞中,油红O监测的细胞内脂质高于对照组和PA培养的细胞。我们的数据证实了脂肪酸在HepG2/C3A细胞生长和功能障碍中的作用,并强调了OA和PA发挥作用的不同机制。
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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
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