Enhancement of IGF-2-induced neurite outgrowth by IGF-binding protein-2 and osteoglycin in SH-SY5Y human neuroblastoma cells
- Authors
- Jeong, Eun Young; Kim, Sujoeng; Jung, Soonwoong; Kim, Gyeongwha; Son, Hyeonwi; Lee, Dong Hoon; Roh, Gu Seob; Kang, Sang Soo; Cho, Gyeong Jae; Choi, Wan Sung; Kim, Hyun Joon
- Issue Date
- Aug-2013
- Publisher
- Elsevier BV
- Keywords
- IGF-2; IGFBP2; Osteoglycin; Neurite outgrowth; SH-SY5Y
- Citation
- Neuroscience Letters, v.548, pp 249 - 254
- Pages
- 6
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Neuroscience Letters
- Volume
- 548
- Start Page
- 249
- End Page
- 254
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/20529
- DOI
- 10.1016/j.neulet.2013.05.038
- ISSN
- 0304-3940
1872-7972
- Abstract
- 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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