Palmitic acid increases apoptosis of neural stem cells via activating c-Jun N-terminal kinase

被引:24
|
作者
Yuan, Qiuhuan [1 ]
Zhao, Shidou [2 ]
Wang, Fuwu [1 ]
Zhang, Hui [1 ]
Chen, Zi-Jiang [2 ]
Wang, Juntao [3 ]
Wang, Zhen [4 ]
Du, Zhaoxia [1 ]
Ling, Eng-Ang [5 ]
Liu, Qian [1 ]
Hao, Aijun [1 ]
机构
[1] Shandong Univ, Dept Histol & Embryol, Shandong Prov Key Lab Mental Disorders, Minist Educ Expt Teratol,Key Lab,Sch Med, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Natl Res Ctr Assisted Reprod Technol & Reprod Gen, Shandong Prov Key Lab Reprod Med, Ctr Reprod Med,Minist Educ,Key Lab Reprod Endocri, Jinan 250021, Shandong, Peoples R China
[3] Shandong Univ, Qi Lu Hosp, Dept Neurosurg, Jinan 250012, Shandong, Peoples R China
[4] Shandong Univ, Sch Med, Inst Physiol, Jinan 250012, Shandong, Peoples R China
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Anat, Singapore 117597, Singapore
基金
中国国家自然科学基金;
关键词
FATTY-ACIDS; HIPPOCAMPAL NEUROGENESIS; OBESITY; INDUCE; DEATH; ACCUMULATION; LIPOTOXICITY; PATHWAYS; EXPOSURE; ROLES;
D O I
10.1016/j.scr.2012.11.008
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Elevated plasma free fatty acid (FFA) level is common in many pathological conditions, including neurological disorders, and their deleterious effects on various cells have been well documented. However, it remains to be investigated whether elevated FFAs would have a direct effect on neural stem cells (NSCs). Here, we reported that palmitic acid (PA) impaired cell viability and increased apoptosis of NSCs significantly in a dose- and time-dependent manner. Increased protein levels of Bax and cleaved caspase 3 coupled with decreased expression of Bcl-2 were also observed in NSCs with increasing dose or time of PA treatment, whereas caspase 3 expression remained relatively unaltered. In parallel to this, the expression of phospho-c-Jun N-terminal kinase (p-JNK) in NSCs challenged with PA was increased significantly; however, JNK expression appeared stable. Remarkably, JNK inhibitor effectively reduced the apoptosis of NSCs induced by PA. The expression of phospho-p38 (p-p38), p38, phospho-extracellular regulated protein kinases 1/2 (p-EKR1/2) and EKR1/2 in NSCs was not affected by PA treatment. In consideration of the above, it is suggested that elevated plasma FFA level may induce apoptosis of NSCs in vivo, and that this might be one of possible underlying mechanisms for the cognitive disturbance in neurological disorders. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 266
页数:10
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