Downregulations of placental fatty acid transporters during cadmium-induced fetal growth restriction

被引:13
|
作者
Xu, Peng [1 ,2 ]
Guo, Huiqin [1 ]
Wang, Huan [1 ]
Lee, Shao Chin [1 ,3 ]
Liu, Ming [4 ,5 ]
Pan, Yongliang [6 ]
Zheng, Jian [7 ]
Zheng, Kang [8 ]
Wang, Huihui [1 ]
Xie, Yuxin [1 ]
Bai, Xiaoxia [9 ]
Liu, Yun [10 ]
Zhao, Meirong [11 ]
Wang, Lan [1 ]
机构
[1] Shanxi Univ, Sch Life Sci, 92 Wucheng Rd, Taiyuan 030006, Shanxi, Peoples R China
[2] Shanghai Jiao Tong Univ, Minist Educ, Bio X Inst, Key Lab Genet Dev & Neuropsychiat Disorders, Shanghai, Peoples R China
[3] Jiangsu Normal Univ, Sch Life Sci, Xuzhou 221116, Jiangsu, Peoples R China
[4] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, Beijing 100101, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[6] Huzhou Univ, Sch Med, Key Lab Vector Biol & Pathogen Control Zhejiang P, Huzhou 313000, Peoples R China
[7] Shanxi Prov Canc Hosp, Dept Cardiopulmonary Funct Examinat, Taiyuan 030013, Shanxi, Peoples R China
[8] Shanxi Prov Canc Hosp, Special Ward, Taiyuan 030013, Shanxi, Peoples R China
[9] Zhejiang Univ, Sch Med, Womens Hosp, Hangzhou 310006, Zhejiang, Peoples R China
[10] Fudan Univ, Pudong Med Ctr, Dept Oncol, Shanghai 201300, Peoples R China
[11] Zhejiang Univ Technol, Coll Environm, Key Lab Microbial Technol Ind Pollut Control Zhej, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Cadmium; Fetal growth restriction; Placenta; Fatty acid transporter; ACTIVATED-RECEPTOR-GAMMA; ACYL-COA SYNTHETASE; BINDING PROTEINS; EPIGENETIC REGULATION; DNA METHYLATION; SKELETAL-MUSCLE; BIRTH-WEIGHT; HEAVY-METALS; EXPOSURE; METABOLISM;
D O I
10.1016/j.tox.2019.05.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cadmium (Cd) is one of the environmental pollutants, which has multiple toxic effects on fetuses and placentas. Placental fatty acid (FA) uptake and transport are critical for the fetal and placental development. We aimed to analyze the triglyceride (TG) level, the expression patterns of several key genes involved in FA uptake and transport, and the molecular mechanisms for the altered gene expressions in placentas in response to Cd treatment. Our results showed that the placental TG level was significantly decreased in the Cd-exposed placentas. Fatty acid transporting protein 1 (FATP1), FATP6 and fatty acid binding protein 3 (FABP3) were significantly down-regulated in the placentas from Cd-exposed mice. The expression level of phospho-p38 MAPK was increased by Cd treatment, while the protein level of total p38 MAPK remained unchanged. The expression levels of peroxisome proliferator-activated receptor-gamma (PPAR-gamma) and the hypoxia-inducible factor-1 alpha (HIF-1 alpha) were significantly decreased in the Cd-exposed placentas. The methylation levels of the promoter regions of FATP1, FATP6 and FABP3 showed no significant differences between the treatment and control groups. In addition, the circulating non-esterified fatty acid (NEFA), total cholesterol (TC), and TG levels were not decreased in the maternal serum from the Cd-exposed mice. Therefore, our results suggest Cd exposure dose not reduce the maternal FA supply, but reduces the placental TG level. Cd treatment also downregulates the placental expressions of FATP1, FATP6 and FABP3, respectively associated with p38-MAPK, p38 MAPK/PPAR-gamma and HIF-1 alpha pathways.
引用
收藏
页码:112 / 122
页数:11
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