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Future directions At least five important questions regarding local IGF-I/IGF-IR signaling warrant future investigation: 1) What are the local sources of IGF-I controlling chondorcyte, osteoblast and osteoclast functions

Research has examined its role in: IGFBP-independent IGF-1R binding and receptor activation studies Myogenic cell proliferation, satellite cell activation, and muscle biology research PI3K/Akt/mTOR and MAPK pathway signalling investigations IGFBP-3 regulation and gene expression modelling in muscle cell cultures Tissue repair and wound healing pathway research Comparative IGF-1 analogue studies alongside IGF-1 LR3 and native IGF-1 Neuroregeneration and CNS biology research models Cell differentiation and anti-apoptotic pathway studies IGF-DES and Myogenic Cell Research Treatment of porcine embryonic myogenic cells with Des(1-3)IGF-1 resulted in a threefold reduction in IGFBP-3 levels in conditioned media, while IGF-1 treatment caused a fourfold increase in the steady-state level of myogenin mRNA suggesting that IGF-I treatment accelerates differentiation of myogenic cells, and that this differentiation may be preceded or accompanied by decreased IGFBP-3 production

Peptides are short chains of amino acids that act as signaling molecules throughout the body

It increases human growth hormone and insulin-like growth factor 1