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Enhancement of IGF-2-induced neurite outgrowth by IGF-binding protein-2 and osteoglycin in SH-SY5Y human neuroblastoma cells
被引:18
|作者:
Jeong, Eun Young
[1
]
Kim, Sujoeng
[1
]
Jung, Soonwoong
[1
]
Kim, Gyeongwha
[1
]
Son, Hyeonwi
[1
]
Lee, Dong Hoon
[1
]
Roh, Gu Seob
[1
]
Kang, Sang Soo
[1
]
Cho, Gyeong Jae
[1
]
Choi, Wan Sung
[1
]
Kim, Hyun Joon
[1
]
机构:
[1] Gyeongsang Natl Univ, Dept Anat & Neurobiol, Inst Hlth Sci, Med Res Ctr Neural Dysfunct,Sch Med, Jinju 660751, South Korea
基金:
新加坡国家研究基金会;
关键词:
IGF-2;
IGFBP2;
Osteoglycin;
Neurite outgrowth;
SH-SY5Y;
GROWTH-FACTOR-BINDING;
LEUCINE-RICH PROTEOGLYCANS;
EXTRACELLULAR-MATRIX;
GENE-EXPRESSION;
FACTOR-II;
INSULIN;
NEURONS;
D O I:
10.1016/j.neulet.2013.05.038
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
A previous study using a mouse model of depression showed that chronic immobilization stress (CIS) reduces levels of insulin-like growth factor (IGF)-2, IGF binding protein 2 (IGFBP2), osteoglycin, and fibromodulin in the amygdala. Here, using human neuroblastoma cells, we tested whether these four proteins cooperatively modulate neuronal plasticity. We found that IGF-2 and IGFBP2 synergistically increased neurite outgrowth via enhanced early signaling through the IGF type 1 receptor. Furthermore, we found that osteoglycin, a small leucine-rich proteoglycan, significantly increased IGF-2/IGFPB2-induced neurite outgrowth, but fibromodulin had no effect. We also found that central amygdala neurons of CIS-induced depressive mouse showed a decreased total dendritic length. These findings suggest that CIS-responsive proteins modulate neuronal morphology during chronic stress. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
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页码:249 / 254
页数:6
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