Neurotoxic effects of ochratoxin A on the subventricular zone of adult mouse brain

被引:31
|
作者
Paradells, Sara [1 ]
Rocamonde, Brenda [1 ]
Llinares, Cristina [1 ]
Herranz-Perez, Vicente [2 ,3 ]
Jimenez, Misericordia [4 ]
Manuel Garcia-Verdugo, Jose [2 ,3 ]
Zipancic, Ivan [1 ,5 ]
Miguel Soria, Jose [1 ,5 ]
Angeles Garcia-Esparza, Ma [1 ,5 ]
机构
[1] Univ CEU Cardenal Herrera, Fac Ciencias Salud, Valencia 46113, Spain
[2] Univ Valencia, Inst Cavanilles Biodiversidad & Biol Evolut, Lab Neurobiol Comparada, CIBERNED, Valencia 46980, Spain
[3] IIS Hosp La Fe UVEG, Unidad Mixta Esclerosis Multiple & Neurorregenera, Valencia 46013, Spain
[4] Univ Valencia, Dept Microbiol & Ecol, E-46100 Burjassot, Spain
[5] Univ CEU Cardenal Herrera, Inst Ciencias Biomed, Moncada 46113, Spain
关键词
Ochratoxin A; mycotoxin; subventricular zone; cell proliferation; cell viability; cell differentiation; NEURAL STEM-CELLS; CELLULAR COMPOSITION; NEUROGENIC REGIONS; STRAND BREAKS; IFN-GAMMA; RAT-BRAIN; IN-VITRO; EXPOSURE; EXPRESSION; MICROGLIA;
D O I
10.1002/jat.3061
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Ochratoxin A (OTA), a mycotoxin that was discovered as a secondary metabolite of the fungal species Aspergillus and Penicillium, is a common contaminant in food and animal feed. This mycotoxin has been described as teratogenic, carcinogenic, genotoxic, immunotoxic and has been proven a potent neurotoxin. Other authors have previously reported the effects of OTA in different structures of the central nervous system as well as in some neurogenic regions. However, the impact of OTA exposure in the subventricular zone (SVZ) has not been assessed yet. To elucidate whether OTA affects neural precursors of the mouse SVZ we investigated, in vitro and in vivo, the effects of OTA exposure on the SVZ and on the neural precursors obtained from this neurogenic niche. In this work, we prove the cumulative effect of OTA exposure on proliferation, differentiation and depletion of neural stem cells cultured from the SVZ. In addition, we corroborated these results in vivo by immunohistochemistry and electron microscopy. As a result, we found a significant alteration in the proliferation process, which was evidenced by a decrease in the number of 5-bromo-2-deoxyuridine-positive cells and glial cells, as well as, a significant decrease in the number of neuroblasts in the SVZ. To summarize, in this study we demonstrate how OTA could be a threat to the developing and the adult SVZ through its impact in cell viability, proliferation and differentiation in a dose-dependent manner. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:737 / 751
页数:15
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