Cell cycle arrest in Batten disease lymphoblast cells

被引:11
|
作者
Kang, Sunyang [1 ]
Kim, June-Bum [2 ]
Heo, Tae-Hwe [3 ]
Kim, Sung-Jo [1 ]
机构
[1] Hoseo Univ, Dept Biotechnol, Asan 336795, Chungnam, South Korea
[2] Seoul Childrens Hosp, Dept Pediat, Seoul 137180, South Korea
[3] Catholic Univ Korea, Integrated Res Inst Pharmaceut Sci, Coll Pharm, Puchon 420743, South Korea
基金
新加坡国家研究基金会;
关键词
Batten disease; Cell cycle arrest; Sphingosine; p21; Glucosylceramide; Sulfatide; NEURONAL CEROID-LIPOFUSCINOSES; INDUCED APOPTOSIS; MOUSE MODELS; INHIBITOR; CLN3; CERAMIDE; SPHINGOSINE-1-PHOSPHATE; DIFFERENTIATION; METABOLISM; PATHWAYS;
D O I
10.1016/j.gene.2013.02.022
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Batten disease is an inherited neurodegenerative disorder caused by a CLN3 gene mutation. Batten disease is characterized by blindness, seizures, cognitive decline, and early death. Although apoptotic cell death is one of the pathological hallmarks of Batten disease, little is known about the regulatory mechanism of apoptosis in this disease. Since the CLN3 gene is suggested to be involved in the cell cycle in a yeast model, we investigated the cell cycle profile and its regulatory factors in lymphoblast cells from Batten disease patients. We found G1/G0 cell cycle arrest in Batten disease cells, with overexpression of p21, sphingosine, glucosylceramide, and sulfatide as possible cell cycle regulators. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 250
页数:6
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