Akt may associate with insulin ‐responsive vesicles via interaction with sortilin

Insulin-responsive vesicles (IRVs) are formed by self-assembly of Glut4, sortilin, insulin-responsive amino peptidase (IRAP), and low-density lipoprotein receptor-related protein 1 (LRP1). TBC1D4 in the insulin signaling pathway binds to the cytoplasmic tails of IRAP and LRP. Here, we demonstrate that the insulin signaling protein Akt interacts with the cytoplasmic tail of sortilin. We suggest that the IRVs represent a scaffold for the final steps of insulin action. Insulin-responsive vesicles (IRVs) deliver the glucose transporter Glut4 to the plasma membrane in response to activation of the insulin signaling cascade: insulin receptor –IRS–PI3 kinase–Akt–TBC1D4–Rab10. Previous studies have shown that Akt, TBC1D4, and Rab10 are compartmentalized on the IRVs. Although functionally significant, the mechanism of Akt association with the IRVs remains unknown. Using pull-down assays, immunofluorescence microscopy, and cross-l inking, we have found that Akt may be recruited to the IRVsvia the interaction with the juxtamembrane domain of the cytoplasmic C terminus of sortilin, a major IRV protein. Overexpression of full-length sortilin increases insulin-stimulated phosphorylation of TBC1D4 and glucose uptake in adipocytes, while overexpression of the cytoplasmic tail of sortilin has the opposite effect. Our findings demonstrate that the IRVs represent both a scaffold and a target of insulin signaling.

Source: FEBS Letters - February 27, 2024 Category: Biochemistry Authors: Nava Zaarur, Anatoli B. Meriin, Maneet Singh, Raghuveera K. Goel, Joseph Zaia, Konstantin V. Kandror Tags: Research Letter Source Type: research