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.
引用
收藏
页码:249 / 254
页数:6
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