Cobalt accumulation and iron-regulatory protein profile expression in immature mouse brain after perinatal exposure to cobalt chloride

被引:10
作者
Petrova, Emilia [1 ]
Pavlova, Ekaterina [1 ]
Tinkov, Alexey A. [2 ,3 ]
Ajsuvakova, Olga P. [2 ,4 ]
Skalny, Anatoly V. [3 ,4 ]
Rashev, Pavel [5 ]
Vladov, Ivelin [1 ]
Gluhcheva, Yordanka [1 ]
机构
[1] Bulgarian Acad Sci, Inst Expt Morphol Pathol & Anthropol Museum, Acad Georgi Bonchev Str,Bl-25, Sofia 1113, Bulgaria
[2] P G Demidov Yaroslavl State Univ, Sovetskaya Str 14, Yaroslavl 150000, Russia
[3] I M Sechenov First Moscow State Med Univ, Moscow 119146, Russia
[4] Russian Acad Sci, Fed Res Ctr Biol Syst & Agrotechnol, Orenburg 460000, Russia
[5] Bulgarian Acad Sci, Acad Kiril Bratanov, Inst Biol & Immunol Reprod, Tsarigradsko Shose Blvd 73, Sofia 1113, Bulgaria
基金
俄罗斯基础研究基金会;
关键词
Cobalt; Iron; Immature brain; Transferrin receptor 1; Hepcidin; Ferroportin; TRANSFERRIN; HEPCIDIN; HYPOXIA; TRAFFICKING; FERROPORTIN; TRANSPORT; PERICYTES; BINDING; CELLS; SERUM;
D O I
10.1016/j.cbi.2020.109217
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
Developing brain is very sensitive to the influence of environmental factors during gestation and the neonatal period. The aim of the study is to assess cobalt and iron accumulation in the brain as well as changes in the expression of iron-regulatory proteins transferrin receptor 1, hepcidin, and ferroportin in suckling mice. Perinatal exposure to cobalt chloride increased significantly cobalt content in brain tissue homogenates of 18-day-old (d18) and 25-day-old (d25) mice inducing alterations in brain iron homeostasis. Higher degree of transferrin receptor 1 expression was demonstrated in cobalt chloride-exposed mice with no substantial changes between d18 and d25 mice. A weak ferroportin expression was found in 18-day-old control and cobalt-treated mouse brain. Cobalt exposure of d25 mice resulted in increased ferroportin expression in brain compared to the un-treated age-matched control group. Hepcidin level in cobalt-exposed groups was decreased in d18 mice and slightly increased in d25 mice. The obtained data contribute for the better understanding of metal toxicity impact on iron homeostasis in the developing brain with further possible implications in neurodegeneration.
引用
收藏
页数:7
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