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中国生物工程杂志

China Biotechnology
China Biotechnology  2019, Vol. 39 Issue (5): 105-113    DOI: 10.13523/j.cb.20190512
    
Advances in Studies on the Structure, Function and Related Antibodies of CD133 (Prominin-1)
Yu-han CHENG,Xi GONG,Yu-ping LUO()
School of Life Sciences, Nanchang University, Nanchang 330031, China
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Abstract  

CD133(Prominin-1) is one of members which are the five-time transmembrane glycoprotein Prominin family. CD133 was originally used as a specific marker for the screening of human hematopoietic stem and progenitor cells, which was subsequently used to isolate and identify specific cell subsets of various cancer stem cells. Many studies have shown that CD133 is a prognostic marker for tumor therapy, interacts with substances such as vascular endothelial growth factor, participates in signal transduction in cell pathways, and plays an important role in maintaining retinal morphology and function. Depending on whether or not it binds to a glycosylation epitope of CD133, antibodies related to CD133 can be classified into glycosylated antibodies, non-glycosylated antibodies, and other antibodies that are not indicated to bind to a glycosylated epitope. The recent years’ research of CD133 was focused,the Prominin family, and the functions, related antibodies and related research methods of CD133 were reviewed.



Key wordsCD133      Prominin-1      Signal pathway      Retina      Antibody     
Received: 08 October 2018      Published: 04 June 2019
ZTFLH:  Q819  
Corresponding Authors: Yu-ping LUO     E-mail: luoyuping@163.com
Cite this article:

Yu-han CHENG,Xi GONG,Yu-ping LUO. Advances in Studies on the Structure, Function and Related Antibodies of CD133 (Prominin-1). China Biotechnology, 2019, 39(5): 105-113.

URL:

https://manu60.magtech.com.cn/biotech/10.13523/j.cb.20190512     OR     https://manu60.magtech.com.cn/biotech/Y2019/V39/I5/105

Fig.1 Schematic representation of the transmembrane glycoprotein, CD133
视网膜疾病 突变位点 突变类型 特征 结果 参考文献
染色体隐性视网膜变性 exon 15
c.1726C>T
p. G576X
纯和无义突变 CD133蛋白被截断 视觉受损
视网膜色素变性
黄斑变性
脉络膜毛细血管萎缩
RPE萎缩
[21,40]
c.1878del G
p. G614EfsX12
纯和移码突变 翻译过早终止
常染色体显性黄斑
变性/营养不良
exon10
c.1117C>T
p. R373C
杂合错义突变 感光盘形态发生被破坏
外节段椎间盘膜
过度生长并错位
RPE萎缩
圆盘膜形态发生异常
进行性中央视觉丧失
[6,42-43]
c.1960C>G
p. L654V
光感受器形态被破坏
常染色体显性Stargardt
样黄斑营养不良
(STGD4-like MD)
c.734T>C
p. L245P
杂合错义突变 损害CD133蛋白稳定性、
灵活性和氨基酸
相互作用网络
中央视觉下降
黄斑萎缩
RPE萎缩
[7]
常染色体隐性视锥-
视杆营养不良
(CORD)
exon 12
c.1349insT
p. Y452fs12X
纯和移码突变 约1/3的CD133
蛋白质被截短
高度近视
视觉严重受损
不同程度的进行性视力
恶化、眩光、色觉异常
和夜视困难
[8,44]
c.2281-26_-17del 纯和内含子缺失 改变了内含子21的剪切
外显子22跳跃
常染色体隐性视
网膜色素变性
(arRP)
exon 8
c.869delG
纯和移码突变 过早引入终止密码子,
约2/3的CD133
蛋白质被截断
早发性黄斑萎缩
近视
[9]
磁盘形态发生和
光感受器退化
Loss of the
CD133 gene
基因缺失
Gene deletion
视力受损
视觉色素异常分布
感光细胞凋亡增加
外节形态受损
渐进性感光器变性
视力完全丧失
[23]
Table 1 Summary of functional studies between CD133 and retinal diseases
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