We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
Ceramide Transporter CERT Is Involved in Muscle Insulin Signaling Defects Under Lipotoxic Conditions.
- Authors
Bandet, Cécile L.; Mahfouz, Rana; Véret, Julien; Sotiropoulos, Athanassia; Poirier, Maxime; Giussani, Paola; Campana, Mélanie; Philippe, Erwann; Blachnio-Zabielska, Agnieszka; Ballaire, Raphaëlle; Liepvre, Xavier Le; Bourron, Olivier; Berkeš, Dušan; Górski, Jan; Ferré, Pascal; Stunff, Hervé Le; Foufelle, Fabienne; Hajduch, Eric; Le Liepvre, Xavier; Le Stunff, Hervé
- Abstract
One main mechanism of insulin resistance (IR), a key feature of type 2 diabetes, is the accumulation of saturated fatty acids (FAs) in the muscles of obese patients with type 2 diabetes. Understanding the mechanism that underlies lipid-induced IR is an important challenge. Saturated FAs are metabolized into lipid derivatives called ceramides, and their accumulation plays a central role in the development of muscle IR. Ceramides are produced in the endoplasmic reticulum (ER) and transported to the Golgi apparatus through a transporter called CERT, where they are converted into various sphingolipid species. We show that CERT protein expression is reduced in all IR models studied because of a caspase-dependent cleavage. Inhibiting CERT activity in vitro potentiates the deleterious action of lipotoxicity on insulin signaling, whereas overexpression of CERT in vitro or in vivo decreases muscle ceramide content and improves insulin signaling. In addition, inhibition of caspase activity prevents ceramide-induced insulin signaling defects in C2C12 muscle cells. Altogether, these results demonstrate the importance of physiological ER-to-Golgi ceramide traffic to preserve muscle cell insulin signaling and identify CERT as a major actor in this process.
- Subjects
CERAMIDES; INSULIN; MUSCLE cells; GLYCOSPHINGOLIPIDS; HYPOGLYCEMIC agents; LIPID metabolism; ANIMAL experimentation; CELL culture; CELLULAR signal transduction; CYTOPLASM; FATTY acids; INSULIN resistance; MICE; MUSCLES; TRANSFERASES
- Publication
Diabetes, 2018, Vol 67, Issue 7, p1258
- ISSN
0012-1797
- Publication type
journal article
- DOI
10.2337/db17-0901