Abstract
Arginine is a semi-essential amino acid with multiple functions, including stimulating the secretion of growth hormone (GH) and insulin-like growth factor 1 (IGF-1). IGF-1, which is produced by hepatocytes, plays important roles in cellular metabolism, proliferation, and growth. Previous studies showed that arginine-induced IGF-1 secretion occurs via two pathways: a GH-dependent pathway and an arginine-dependent pathway with an unknown mechanism. In this study, we identified the mechanisms regulating IGF-1 secretion. First, GH stimulates the translation of IGF-1 and increases IGF-1 protein levels, leading to IGF-1 secretion. As observed in fasted mice and hepatocytes cultivated in arginine-depleted medium, decreases in arginine concentrations resulted in IGF-1 retention in the endoplasmic reticulum. Arginine administration reverses this retention, leading to IGF-1 secretion. These data describe a novel IGF-1 secretion control system in the endoplasmic reticulum.