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Loss of iron from mouse peritoneal macrophages in vitro after uptake of (55fe)ferritin and (55fe)ferritin rabbit antiferritin complexes.小鼠腹腔巨噬细胞摄取(55铁)铁蛋白和(55铁)铁蛋白兔抗铁蛋白复合物后,体外铁流失情况。
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The separation, long-term cultivation, and maturation of the human monocyte.人单核细胞的分离、长期培养及成熟
J Exp Med. 1977 Dec 1;146(6):1613-26. doi: 10.1084/jem.146.6.1613.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
The tagging of red cells and plasma proteins with radioactive chromium.用放射性铬标记红细胞和血浆蛋白。
J Clin Invest. 1950 Dec;29(12):1604-13. doi: 10.1172/JCI102403.
3
Iron and protein kinetics studied by means of doubly labeled human crystalline transferrin.通过双标记人晶体转铁蛋白研究铁和蛋白质动力学。
J Clin Invest. 1961 Dec;40(12):2143-52. doi: 10.1172/JCI104440.
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A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY.一种用于电子显微镜的简化柠檬酸铅染色法。
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THE DIFFERENTIATION OF MONONUCLEAR PHAGOCYTES. MORPHOLOGY, CYTOCHEMISTRY, AND BIOCHEMISTRY.单核吞噬细胞的分化。形态学、细胞化学与生物化学
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DISC ELECTROPHORESIS. I. BACKGROUND AND THEORY.圆盘电泳。一、背景与理论。
Ann N Y Acad Sci. 1964 Dec 28;121:321-49. doi: 10.1111/j.1749-6632.1964.tb14207.x.
7
ON FERRITIN AND ITS PRODUCTION BY CELLS GROWING.关于铁蛋白及其由正在生长的细胞产生的情况。
Lab Invest. 1963 Oct;12:1026-39.
8
The plasma-to-cell cycle of transferrin.转铁蛋白的血浆到细胞周期。
J Clin Invest. 1963 Mar;42(3):314-26. doi: 10.1172/JCI104718.
9
The role of chelation and binding equilibria in iron metabolism.
Arch Biochem Biophys. 1960 Jun;88:222-6. doi: 10.1016/0003-9861(60)90226-5.
10
Determination of microgram quantities of deoxyribonucleic acid and protein in tissues grown in vitro.体外培养组织中微克量脱氧核糖核酸和蛋白质的测定
Arch Biochem Biophys. 1957 Feb;66(2):340-53. doi: 10.1016/s0003-9861(57)80009-5.

小鼠腹腔巨噬细胞摄取(55铁)铁蛋白和(55铁)铁蛋白兔抗铁蛋白复合物后,体外铁流失情况。

Loss of iron from mouse peritoneal macrophages in vitro after uptake of (55fe)ferritin and (55fe)ferritin rabbit antiferritin complexes.

作者信息

Fedorko M E

出版信息

J Cell Biol. 1974 Sep;62(3):802-14. doi: 10.1083/jcb.62.3.802.

DOI:10.1083/jcb.62.3.802
PMID:4859401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2109210/
Abstract

Mouse peritoneal macrophages in culture for 24 h were exposed to horse [(55)Fe]ferritin and rabbit antihorse [(55)Fe]ferritin antibody complex and the amount of (55)Fe in the medium was assayed up to 2 days after the pulse uptake. Cell survival was assayed by photographing the same areas of the tissue culture Petri dish on successive days and by counting cell numbers per unit area. In experiments in which quantitative assay for cell death is negligible, about 10-20% of the iron ingested by pinocytosis or phagocytosis is released to iron-free medium containing either freshly dialyzed or deironized newborn calf serum (10%). Over the 2-day postpulse period, iron loss is linear. This loss of iron to the medium is significantly reduced by adding iron-saturated newborn calf serum in the postpulse recovery period. A significant portion of the iron released to the medium is bound to transferrin. When human serum is used in the tissue culture system, similar quantities (10-25%) of the ingested iron are lost to the medium 2 days after the pulse.

摘要

将培养24小时的小鼠腹腔巨噬细胞暴露于马[(55)铁]铁蛋白和兔抗马[(55)铁]铁蛋白抗体复合物中,并在脉冲摄取后长达2天的时间内测定培养基中(55)铁的含量。通过连续几天拍摄组织培养培养皿的相同区域并计数每单位面积的细胞数量来测定细胞存活率。在细胞死亡定量测定可忽略不计的实验中,通过胞饮作用或吞噬作用摄取的铁中约10%-20%会释放到含有新鲜透析或去铁新生小牛血清(10%)的无铁培养基中。在脉冲后的2天内,铁的损失呈线性。在脉冲后恢复期加入铁饱和的新生小牛血清可显著减少铁向培养基中的损失。释放到培养基中的铁的很大一部分与转铁蛋白结合。当在组织培养系统中使用人血清时,脉冲后2天,摄入的铁也有相似数量(10%-25%)损失到培养基中。