Gut-on-a-chip for exploring the transport mechanism of Hg(II)

被引:28
|
作者
Wang, Li [1 ,2 ]
Han, Junlei [1 ,2 ]
Su, Weiguang [1 ,2 ]
Li, Anqing [1 ,2 ]
Zhang, Wenxian [1 ,2 ]
Li, Huimin [1 ,2 ]
Hu, Huili [3 ,4 ,5 ]
Song, Wei [6 ]
Xu, Chonghai [1 ,2 ]
Chen, Jun [1 ,2 ]
机构
[1] Qilu Univ Technol, Shandong Acad Sci, Sch Mech Engn, Jinan 250353, Peoples R China
[2] Shandong Inst Mech Design & Res, Jinan 250353, Peoples R China
[3] Shandong Univ, Sch Basic Med Sci, Key Lab Expt Teratol, Minist Educ, Jinan 250012, Peoples R China
[4] Shandong Univ, Sch Basic Med Sci, Dept Genet, Jinan 250012, Peoples R China
[5] Shandong Univ, Cheeloo Med Coll, Res Ctr Stem Cell & Regenerat Med, Sch Basic Med Sci, Jinan 250012, Peoples R China
[6] Shandong Univ, Shandong Prov Hosp, Dept Oncol, Jinan 250021, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
INORGANIC MERCURY; ABSORPTION; CACO-2;
D O I
10.1038/s41378-022-00447-2
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Animal models and static cultures of intestinal epithelial cells are commonly used platforms for exploring mercury ion (Hg(II)) transport. However, they cannot reliably simulate the human intestinal microenvironment and monitor cellular physiology in situ; thus, the mechanism of Hg(II) transport in the human intestine is still unclear. Here, a gut-on-a-chip integrated with transepithelial electrical resistance (TEER) sensors and electrochemical sensors is proposed for dynamically simulating the formation of the physical intestinal barrier and monitoring the transport and absorption of Hg(II) in situ. The cellular microenvironment was recreated by applying fluid shear stress (0.02 dyne/cm(2)) and cyclic mechanical strain (1%, 0.15 Hz). Hg(II) absorption and physical damage to cells were simultaneously monitored by electrochemical and TEER sensors when intestinal epithelial cells were exposed to different concentrations of Hg(II) mixed in culture medium. Hg(II) absorption increased by 23.59% when tensile strain increased from 1% to 5%, and the corresponding expression of Piezo1 and DMT1 on the cell surface was upregulated.
引用
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页数:13
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