Overexpression of protocadherin 7 inhibits neuronal survival by downregulating BIRC5 in vitro

被引:13
|
作者
Xiao, Huajuan [1 ]
Sun, Ziling [1 ]
Wan, Jun [1 ,2 ]
Hou, Shengtao [3 ,4 ]
Xiong, Yi [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Med Ctr, Shenzhen Peking Univ, Shenzhen Key Lab Neuronal Struct Biol,Biomed Res, Shenzhen, Peoples R China
[2] Hong Kong Univ Sci & Technol, Div Life Sci, Hong Kong, Hong Kong, Peoples R China
[3] Southern Univ Sci & Technol, Brain Res Ctr, Shenzhen, Peoples R China
[4] Southern Univ Sci & Technol, Dept Biol, Shenzhen, Peoples R China
关键词
Protocadherin; 7; BIRC5; Whole transcriptome sequencing; Apoptosis; Neuropathology; NON-CLUSTERED PROTOCADHERIN; CADHERIN SUPERFAMILY; DELTA-PROTOCADHERINS; GAMMA-PROTOCADHERINS; NF-PROTOCADHERIN; BRAIN; EXPRESSION; CANCER; PP2A; SET;
D O I
10.1016/j.yexcr.2018.03.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Protocadherins (Pcdhs) are widely-expressed transmembrane proteins in the nervous system. Recent studies suggest that Pcdhs play multiple critical roles during neuronal development. However, the cellular mechanisms of Pcdh7 in neurons are still largely unknown. In the current study, we demonstrated that the expression of Pcdh7 during mouse brain development was regulated spatiotemporally. We observed that the elevated expression of Pcdh7 led to activation of the intrinsic apoptotic pathway in primary cortical neurons. Whole transcriptome sequencing revealed that 12 genes were involved in the apoptotic pathway including baculoviral inhibitor of apoptosis (IAP) repeat containing 5 (BIRC5). The neuronal apoptosis caused by Pcdh7 over expression could be significantly inhibited by either a missense mutation in the conserved motif CM2 domain of Pcdh7 or BIRC5 overexpression. These results suggest the existence of Pcdh7-BIRC5 signaling cascade in the cortical neurons and represent a potential therapeutic area for further investigation.
引用
收藏
页码:71 / 80
页数:10
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