The effect of Insulin like growth factor-I (IGF-I) and IGF binding protein-3 (IGFBP-3) on cellular proliferation in mouse 3T3 fibroblast cells.
10.4046/trd.1999.47.5.618
- Author:
Chul Ho CHO
1
;
Seung Min KWAK
;
Tae Hun MOON
;
Jae Hwa CHO
;
Jeong Seon RYU
;
Hyong Lyeol LEE
Author Information
1. Department of Internal Medicine, Inha University College of Medicine, Sungnam, Kyunggi-Do, Korea. ch4cho@chollian.net
- Publication Type:Original Article
- Keywords:
Insulin-like growth factor-I (IGF-I);
Insulin-like growth factor binding protein (IGFBP);
Mitogen
- MeSH:
3T3 Cells;
Animals;
Blotting, Northern;
Blotting, Western;
Cell Death;
Cell Proliferation*;
Culture Media, Serum-Free;
Fibroblasts*;
Insulin*;
Insulin-Like Growth Factor Binding Protein 3;
Insulin-Like Growth Factor Binding Proteins;
Insulin-Like Growth Factor I;
Mice*;
Phosphorylation;
Receptor, IGF Type 1;
RNA, Messenger
- From:Tuberculosis and Respiratory Diseases
1999;47(5):618-628
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Cell growth is a balance between cell proliferation and cell death. Insulin-like growth factor-I(IGF-I), which binds IGF-I receptor (IGF-IR), mediates cellular proliferation as a potent mitogen. IGF binding protein-3 (IGFBP-3) as a circulating major IGFBP can inhibit or enhance the effects of IGF-I on cellular growth by binding IGFs. METHODS: We investigated the expressions of mRNA of IGF-I and IGF-IR by northern blot and phosphorylation of IGF-IR with the treatment of IGF-I by western blot in 3T3 fibroblast cells. The cellular proliferations of 3T3 cells with the treatments of IGF-I were evaluated using 3H-thymidine incorporation and MTT assay. Also to observe the effect of IGFBP-3 on cellular proliferation, 3T3 cells were treated with anti-IGFBP-3 and alpha IR3(monoclonal antibody to IGF-IR) alone or in combination. RESULTS: Our results demonstrated that 3T3 cells showed mRNA expressions of IGF-I and IGF-IR and the IGF-I increased phosphorylation of IGF-IR. The treatments of 3T3 cells with IGF-I increased cellular proliferation in 5% and 1% seruma-containing media, not in serum-free media. The addition of anti-IGFBP-3 to neutralize IGFBP-3 showed 2-fold increase of cellular proliferation, and also co-incubation of anti-IGFBP-3 and alpha IR3 together showed similar increase of cellular proliferation in 3T3 cells. Interestingly, when the cells were prethreated with alpha IR3 for 4 hr, prior to the simultaneous addition of alpha IR3 and anti-IGFBP-3, anti-IGFBP-3-mediated cellular proliferation was decreased to control level. All of these results suggest that free IGF-I released from IGF-I/IGFBP-3 complex would be involved in the cellular proliferation. CONCLUSION: IGF-I action by binding IGF-I.
