
pmid: 26804653
Transthyretin (TTR) has a neuroprotective role in the central nervous system (CNS) in Alzheimer's disease (AD) and cerebral ischemia. Increased levels of TTR and activated insulin-like growth factor I receptor (IGF-IR) are associated with reduced neurodegeneration in an AD mouse model. In the present study, we found that TTR and IGF-I have a synergistic effect on activation of one of the IGF-IR signaling pathways. Hippocampus of TTR null mice present decreased levels of phosphorylated IGF-IR and Akt when compared with TTR wild type littermate animals. Cell studies reveal the synergistic effect of TTR and IGF-I in promoting IGF-IR signaling even under glutamate induced toxicity. TTR:IGF-IR complexes are identified and a bio-layer interferometry assay demonstrated an interaction between TTR and IGF-IR with a KD ranging from 99 to 744nM. In summary, our results point to a new TTR role through the IGF-I axis, mediated through TTR-IGF-IR interactions.
Mice, Knockout, Hippocampus, Receptor, IGF Type 1, Disease Models, Animal, Mice, Alzheimer Disease, Molecular Medicine, Animals, Prealbumin, Insulin-Like Growth Factor I, Molecular Biology, Proto-Oncogene Proteins c-akt, Signal Transduction
Mice, Knockout, Hippocampus, Receptor, IGF Type 1, Disease Models, Animal, Mice, Alzheimer Disease, Molecular Medicine, Animals, Prealbumin, Insulin-Like Growth Factor I, Molecular Biology, Proto-Oncogene Proteins c-akt, Signal Transduction
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