Receptor-mediated uptake of ferritin-bound iron by human intestinal Caco-2 cells.

Receptor-mediated uptake of ferritin-bound iron by human intestinal Caco-2 cells.
复制标题

DOI:
10.1016/j.jnutbio.2008.04.003
复制
发表时间:
2009-04
影响因子:
5.6
通讯作者:
Lonnerdal, Bo
Lonnerdal, Bo
中科院分区:
医学2区
文献类型:
--
作者:
Kalgaonkar, Swati;Lonnerdal, Bo

文献摘要

参考文献

被引文献

相似文献

Ferritin (Ft) is a large iron-binding protein (~450 kDa) that is found in plant and animal cells and can sequester up to 4,500 iron (Fe) atoms per Ft molecule. Our previous studies on intestinal Caco-2 cells have shown that dietary factors affect the uptake of Fe from ferritin in a manner different from that of Fe from FeSO4, suggesting a different mechanism for cellular uptake. The objective of this study was to determine the mechanism for Ft-Fe uptake using Caco-2 cells. Binding of 59Fe-labeled Ft at 4° C showed saturable kinetics and Scatchard analysis resulted in a KD of 1.6 μM, strongly indicating a receptor-mediated process. Competitive binding studies with excess unlabelled Ft significantly reduced binding and uptake studies at 37° C showed saturation after 4 h. Enhancing and blocking endocytosis using Mas-7 (a G-protein activator) and hypertonic medium (0.5 M sucrose), respectively, demonstrated that Ft-Fe uptake by Mas-7 treated cells was 140% of control cells, whereas sucrose treatment resulted in a statistically significant reduction in Ft-Fe uptake by 70% as compared to controls. Inhibition of macropinocytosis with 5-(N,N-dimethyl)-amiloride (Na+/H+ antiport blocker) resulted in a decrease (by ~20%) in Ft-Fe uptake at high concentrations of Ft, suggesting that enterocytes can use more than one Ft-uptake mechanism in a concentration dependent manner. These results suggest that Ft uptake by enterocytes is carried out via endocytosis when Ft levels are within a physiological range, whereas Ft at higher concentrations may be absorbed using the additional mechanism of macropinocytosis.
DOI: 10.1002/hep.1840110514
发表时间: 1990-05-01
期刊: HEPATOLOGY
影响因子: 13.5
作者:
ADAMS, PC;CHAU, LA
通讯作者: CHAU, LA
DOI: 10.1021/jf011046u
发表时间: 2002-01-16
影响因子: 6.1
作者:
Glahn, RP;Wortley, GM;Miller, DD
通讯作者: Miller, DD
DOI: 10.1152/ajpgi.00443.2001
发表时间: 2002-11-01
影响因子: 4.5
作者:
Follett, JR;Suzuki, YA;Lönnderdal, B
通讯作者: Lönnderdal, B
DOI: 10.1093/ajcn/40.1.42
发表时间: 1984-01-01
影响因子: 7.1
作者:
LYNCH, SR;BEARD, JL;COOK, JD
通讯作者: COOK, JD
DOI: 10.1016/j.jnutbio.2007.02.001
发表时间: 2008-01-01
影响因子: 5.6
作者:
Kalgaonkar, Swati;Loennerdal, Bo
通讯作者: Loennerdal, Bo