Growth and Differentiation Factor 11 (GDF11) and GDF8 are two closely related molecules of the larger TGF? superfamily. While GDF8 is well known for its role in the regulation of muscle mass, evidence is now emerging that implicates GDF11 as a factor that has beneficial effects on multiple biological systems. Both GDF11 and GDF8 are tightly regulated by multiple mechanisms. Each ligand is made as a precursor with an N-terminal prodomain that remains noncovalently bound to the mature, keeping the signaling component latent until activated by Tolloid-like proteases. In addition, extracellular antagonists such as Follistatin and GASP bind and block ligand signaling. We propose that GDF11 and GDF8 are present in the serum in multiple activity states ranging from a latent form to an activated form. However, studies that investigate how the different activity states are differentially regulated are limited. We rationalize that a better understanding of these mechanisms will facilitate efforts to understand the systemic role of GDF11 and GDF8 in human biology and the aging process. To achieve this objective, we will use a combination of biochemical and molecular approaches coupled with in vitro and in vivo experiments. Our proposal is centered on three specific aims where we will (1) test the hypothesis that GDF11 and GDF8 exists in multiple ?activity? states that regulate a transition from a latent state to an active state, (2) test the hypothesis that the ?net? GDF11/GDF8 activity in serum decreases with age, and (3) test the hypothesis that GDF11 signaling and its regulation/extracellular antagonism can be decoupled. Collectively, these aims will provide a better understanding of the mechanisms of extracellular regulation of GDF11 and GDF8 and how these potentially change during the aging process. Furthermore, we expect to produce novel GDF11 and GDF8 molecules that can be used as tools to further probe the mechanisms associated with GDF11 and aging, and can also be used to restore youthful levels of GDF11 in aged animals.
Ligands in the TGF? family, specifically GDF11 and GDF8, have been implicated in regulating biological process affected by aging. Our work will characterize the different molecular states of GDF11 and GDF8 to help better understand how their activity is regulated by extracellular mechanisms during the aging process.
