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Biochimica et biophysica acta. Molecular basis of disease, 2024-06, Vol.1870 (5), p.167173-167173, Article 167173
2024

Details

Autor(en) / Beteiligte
Titel
Caveolin-2 palmitoylation turnover facilitates insulin receptor substrate-1-directed lipid metabolism by insulin receptor tyrosine kinase
Ist Teil von
  • Biochimica et biophysica acta. Molecular basis of disease, 2024-06, Vol.1870 (5), p.167173-167173, Article 167173
Ort / Verlag
Netherlands: Elsevier B.V
Erscheinungsjahr
2024
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • Here, we show that insulin induces palmitoylation turnover of Caveolin-2 (Cav-2) in adipocytes. Acyl protein thioesterases-1 (APT1) catalyzes Cav-2 depalmitoylation, and zinc finger DHHC domain-containing protein palmitoyltransferase 21 (ZDHHC21) repalmitoylation of the depalmitoylated Cav-2 for the turnover, thereby controlling insulin receptor (IR)-Cav-2-insulin receptor substrate-1 (IRS-1)-Akt-driven signaling. Insulin-induced palmitoylation turnover of Cav-2 facilitated glucose uptake and fat storage through induction of lipogenic genes. Cav-2-, APT1-, and ZDHHC21-deficient adipocytes, however, showed increased induction of lipolytic genes and glycerol release. In addition, white adipose tissues from insulin sensitive and resistant obese patients exhibited augmented expression of LYPLA1 (APT1) and ZDHHC20 (ZDHHC20). Our study identifies the specific enzymes regulating Cav-2 palmitoylation turnover, and reveals a new mechanism by which insulin-mediated lipid metabolism is controlled in adipocytes. •APT1 depalmitoylates Cav-2 to initiate palmitoylation turnover•ZDHHC21 repalmitoylates the depalmitoylated Cav-2 by APT1.•The Cav-2 palmitoylation turnover controls glucose uptake and fat storage in adipocytes.•Cav-2 palmitoylation turnover modulates insulin-induced lipogenesis and lipolysis.

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