The changes of miRNA expression in rat hippocampus following chronic lead exposure

被引:72
作者
An, Jun
Cai, Tongjian
Che, Honglei
Yu, Tao
Cao, Zipeng
Liu, Xinqin
Zhao, Fang
Jing, Jinfei
Shen, Xuefeng
Liu, Mingchao
Du, Kejun
Chen, Jingyuan
Luo, Wenjing [1 ]
机构
[1] Fourth Mil Med Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNAs; Lead; Neurotoxicity; Rats; Hippocampus; NF-KAPPA-B; INOSITOL TRIPHOSPHATE RECEPTOR; CENTRAL-NERVOUS-SYSTEM; HUMAN BRAIN-CELLS; PROTEIN-KINASE; MICRORNA REGULATION; NONCODING RNAS; UP-REGULATION; ACTIVATION; NEUROTOXICITY;
D O I
10.1016/j.toxlet.2014.06.002
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
miRNAs have been found to contribute to normal brain functions, nervous system diseases, as well as neurotoxicities induced by external agents. However, whether they are involved in lead-induced neurotoxicities is still not clear. To identify that, a lead-induced chronic neurotoxicity model of rats was built. Both miRNA microarray analysis and qRT-PCR were performed to determine the change of miRNA expression in hippocampus. Then 3 bioinformatics databases were used to analyze the relative target genes of these miRNA, which were further confirmed by qRT-PCR and Western blot. In the present study, lead exposure resulted in the changed expression of 7 miRNAs: miR-204, miR-211, miR-448, miR-449a, miR-34b, and miR-34c were greatly up-regulated while miR-494 was greatly down-regulated. Bioinformatics analysis results showed that the target genes of 6 up-regulated miRNAs were related to neural injury and neurodegeration, axon and synapse function, neural development and regeneration. Correspondingly, the expression levels of mature mRNAs and proteins of three target genes (Bcl-2, Itpr1, and Map2k1) were greatly repressed, verifying the results of bioinformatics analysis. Taken together, our results showed that the expression of several miRNAs reported to be associated with neurophysiological pathways and neurodegenerative diseases changed in rat hippocampus following chronic lead exposure. These miRNAs may play important roles in lead-induced neurotoxicity. (C) 2014 Published by Elsevier Ireland Ltd.
引用
收藏
页码:158 / 166
页数:9
相关论文
共 63 条
[1]
Sex and rearing condition modify the effects of perinatal lead exposure on learning and memory [J].
Anderson, D. W. ;
Pothakos, K. ;
Schneider, J. S. .
NEUROTOXICOLOGY, 2012, 33 (05) :985-995
[2]
MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]
The neurotoxicity of environmental aluminum is still an issue [J].
Bondy, Stephen C. .
NEUROTOXICOLOGY, 2010, 31 (05) :575-581
[4]
Assessing windows of susceptibility to lead-induced cognitive deficits in Mexican children [J].
Braun, Joe M. ;
Hoffman, Elaine ;
Schwartz, Joel ;
Sanchez, Brisa ;
Schnaas, Lourdes ;
Mercado-Garcia, Adriana ;
Solano-Gonzalez, Maritsa ;
Bellinger, David C. ;
Lanphear, Bruce P. ;
Hu, Howard ;
Tellez-Rojo, Martha M. ;
Wright, Robert O. ;
Hernandez-Avila, Mauricio .
NEUROTOXICOLOGY, 2012, 33 (05) :1040-1047
[5]
MicroRNA regulation of neural plasticity and memory [J].
Bredy, Timothy W. ;
Lin, Quan ;
Wei, Wei ;
Baker-Andresen, Danay ;
Mattick, John S. .
NEUROBIOLOGY OF LEARNING AND MEMORY, 2011, 96 (01) :89-94
[6]
Cao XW, 2006, ANNU REV NEUROSCI, V29, P77, DOI 10.1146/annurev.neuro.29.051605.112839
[7]
Loss of mitogen-activated protein kinase kinase kinase 4 (MEKK4) results in enhanced apoptosis and defective neural tube development [J].
Chi, HB ;
Sarkisian, MR ;
Rakic, P ;
Flavell, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3846-3851
[9]
Spatial and temporal patterns of ERK signaling during mouse embryogenesis [J].
Corson, LB ;
Yamanaka, Y ;
Lai, KMV ;
Rossant, J .
DEVELOPMENT, 2003, 130 (19) :4527-4537
[10]
ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852