IA-2 modulates dopamine secretion in PC12 cells

被引:12
作者
Nishimura, Takuya [1 ]
Harashima, Shin-ichi [1 ,2 ]
Hu Yafang [1 ,3 ]
Notkins, Abner Louis [1 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Expt Med Sect, Oral Infect & Immun Branch, NIH, Bethesda, MD 20892 USA
[2] Kyoto Univ, Dept Diabet & Clin Nutr, Grad Sch Med, Kyoto, Japan
[3] Childrens Natl Med Ctr, Ctr Canc & Immunol Res, Washington, DC 20010 USA
基金
美国国家卫生研究院;
关键词
IA-2; siRNA; PC12; Dopamine; Hormones; Neurotransmitters; PROTEIN-TYROSINE-PHOSPHATASE; DEPENDENT DIABETES-MELLITUS; INSULIN-SECRETION; TRANSMEMBRANE PROTEIN; TARGETED DISRUPTION; MOLECULAR-CLONING; DOUBLE KNOCKOUT; AUTOANTIGEN; IA-2-BETA; MICE;
D O I
10.1016/j.mce.2009.09.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The secretion of the hormone insulin from beta cells is modulated by the expression of the dense core vesicle transmembrane protein IA-2. Since IA-2 is found in neuroendocrine cells throughout the body, the present experiments were initiated to determine whether the expression of IA-2 also modulates the secretion of neurotransmitters. Using the dopamine-secreting pheochromocytoma cell line PC12, we found that the overexpressions of IA-2 increased the cellular content and secretion of dopamine, whereas the knockdown of IA-2 by siRNA decreased the cellular content and secretion of dopamine. Neither the overexpression nor knockdown of IA-2 influenced the uptake of [H-3]dopamine by PC12 cells, but did influence the amount of [H-3]dopamine secreted. Overexpression of IA-2 also increased the level of the dense core vesicle-associated proteins Rab3A, IA-2 beta and secretogranin II, whereas the knockdown of IA-2 decreased the level of these proteins. We conclude that the expression of IA-2 profoundly influences the function of dense core vesicles and has a broad modulating effect on the cellular content and secretion of both hormones and neurotransmitters. Published by Elsevier Ireland Ltd.
引用
收藏
页码:81 / 86
页数:6
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