Kinetics of manganese transport and gene expressions of manganese transport carriers in Caco-2 cell monolayers

被引:25
作者
Li, Xiaoli [1 ,2 ]
Xie, Jingjing [1 ]
Lu, Lin [1 ]
Zhang, Liyang [1 ]
Zhang, Lingyan [1 ]
Zou, Yaxue [3 ]
Wang, Qiuyue [3 ]
Luo, Xugang [1 ]
Li, Sufen [3 ]
机构
[1] Chinese Acad Agr Sci, Inst Anim Sci, Mineral Nutr Res Div, Beijing 100193, Peoples R China
[2] Henan Univ Sci & Technol, Coll Anim Sci & Technol, Luoyang 471003, Peoples R China
[3] Hebei Normal Univ Sci & Technol, Dept Anim Sci, Key Lab Prevent Vet Med Hebei Prov, Qinhuangdao 066004, Peoples R China
基金
中国国家自然科学基金;
关键词
Manganese; Transport; Divalent metal transporter 1; Ferroportin; Caco-2; cell; INTESTINAL EPITHELIAL-CELLS; IN-VITRO; IRON UPTAKE; COPPER UPTAKE; LINE CACO-2; ABSORPTION; MODEL; COLON; METABOLISM; CULTURE;
D O I
10.1007/s10534-013-9670-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two experiments were conducted to investigate the kinetics of manganese (Mn) transport in Caco-2 cell monolayers and the gene expressions of Mn transport carriers in apical (AP) and basolateral (BL) membranes. In experiment 1, the cells were treated with the medium containing 146 mu mol/L of Mn (MnSO4 center dot H2O). Both the uptake and transport of Mn from AP-BL or from BL-AP at different time-points were assessed to determine the optimal time for kinetics of Mn transport. The transport of Mn increased linearly with higher efficiency values in AP-BL than in BL-AP direction, however, the uptake of Mn revealed an asymptotic pattern within 120 min. In experiment 2, the kinetics of Mn transport in AP-BL was determined with media containing Mn concentrations from 0 to 2,500 mu mol/L at 40 and 120 min, respectively, and mRNA levels of divalent metal transporter 1 (DMT1) and ferroportin (FPN1) were determined in Caco-2 cells treated with the medium containing 0 or 800 mu mol/L of Mn for 120 min. The kinetics of Mn transport showed a carrier-mediated process when Mn concentrations were lower than 1,000 mu mol/L and a linear increment when Mn concentrations exceeded 1,000 mu mol/L at either 40 or 120 min. Mn treatment decreased (P < 0.01) DMT1 mRNA level and increased (P < 0.01) FPN1 mRNA level. The results from the present study suggested that Mn transport in AP-BL fit both carrier-mediated saturable and non-saturable diffusion processes, and Mn transport carriers DMT1 and FPN1 mediate the apical uptake and basolateral exit of Mn in Caco-2 cells.
引用
收藏
页码:941 / 953
页数:13
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