Table 1.
System | Source of IGFBP-5 | Effects observed | References | |
---|---|---|---|---|
Stimulatory effects | Mouse osteoblasts in primary culture | Mammalian cell culture | Increase in thymidine incorporation into DNA | [16] |
MC3T3, human osteoblasts in primary culture | E. coli-derived | Increase in thymidine incorporation into DNA | [43] | |
MG63, human osteoblasts in primary culture | E. coli-derived | Increases in osteocalcin and alkaline phosphatase | [41] | |
Wild type and IGF-I-deficient mice
In vitro-calvarial osteoblasts In vivo-injection in parietal bones |
E. coli-derived |
In vitro - increase in thymidine incorporation into DNA and alkaline phophatase activity
In vivo - increase in alkaline phophatase and osteocalcin mRNA |
[40] | |
Local or systemic injections of IGFBP-5 and IGF-I in rats | E. coli-derived | Increase in cortical bone formation, bone area, bone mineral density | [39] | |
Mouse osteosarcoma cells (OS/50K8) | Expression plasmid | Increase in osteocalcin mRNA | [44] | |
Inhibitory effects | U2 osteosarcoma cells | Mammalian-cell culture | IGF-I-mediated cell proliferation inhibited | [19] |
Mouse osteosarcoma cells | Expression plasmid | Increase in cell doubling time (decrease in proliferation by 30%) | [44] | |
MC3T3 | Retrovirus | Decreased mRNAs of osteoblast specific genes; decreased bone mineralization | [47] | |
IGFBP-5 transgenic mice | Systemic expression via β-actin promoter | Decrease in bone mineral density and mineralization | [46] | |
IGFBP-5 transgenic mice | Osteoblast-specific expression | Transient decrease mineral apposition;in decreased trabecular bone volume and osteopenia | [45] |