Abstract
IGF-I regulates islet β-cell growth, survival, and metabolism and protects against type 1 diabetes (T1D). However, the therapeutic efficacy of free IGF-I may be limited by its biological half-life in vivo. We investigated whether prolongation of its half-life as an IGF-I/IGF binding protein (IGFBP)-3 complex affords increased protection against T1D and whether this occurs by influencing T cell function and/or islet β-cell growth and survival. Administration of IGF-I either alone or as an IGF-I/IGFBP-3 complex reduced the severity of insulitis and delayed the onset of T1D in nonobese diabetic mice, but IGF-I/IGFBP-3 was significantly more effective. Protection from T1D elicited by IGF-I/IGFBP-3 was mediated by up-regulated CCL4 and down-regulated CCL3 gene expression in pancreatic draining lymph nodes, activation of the phosphatidylinositol 3-kinase and Akt/protein kinase B signaling pathway of β-cells, reduced β-cell apoptosis, and stimulation of β-cell replication. Reduced β-cell apoptosis resulted from elevated Bcl-2 and Bcl-XL activity and diminished caspase-9 activity, indicating a novel role for a mitochondrial-dependent pathway of β-cell death. Thus, IGF-I/IGFBP-3 affords more efficient protection from insulitis, β-cell destruction, and T1D than IGF-I, and this complex may represent an efficacious therapeutic treatment for the prevention of T1D.
Inhibition of Cytokine-Induced β Cell Apoptosis via Laccase and Its Therapeutic Advantages for Insulin-Dependent Diabetes Mellitus, Type 1 Diabetes