Fitm2 is required for ER homeostasis and normal function of murine liver Institutional Repository Document uri icon

abstract

  • ABSTRACTThe ER-resident protein fat-inducing transcript 2 (FIT2) catalyzes acyl-CoA cleavage in vitro and is required for endoplasmic reticulum (ER) homeostasis and normal lipid storage in cells. The gene encoding FIT2 is essential for the viability of mice and worms. Whether FIT2 acts as an acyl-CoA diphosphatase in vivo and how this activity affects liver, where the protein was discovered, are unknown. Here, we report that hepatocyte-specific Fitm2 knockout (FIT2-LKO) mice exhibited elevated acyl-CoA levels, ER stress, and signs of liver injury. FIT2-LKO mice fed a chow diet had more triglycerides in their livers than control littermates due, in part, to impaired secretion of triglyceride-rich lipoproteins and reduced capacity for fatty acid oxidation. Challenging FIT2-LKO mice with a high-fat diet to increase FIT2 acyl-CoA substrates worsened hepatic ER stress and liver injury, but unexpectedly reversed the steatosis phenotype, similar to what is observed in FIT2-deficient cells loaded with fatty acids. Our findings support the model that FIT2 acts as an acyl-CoA diphosphatase in vivo and is crucial for normal hepatocyte function and ER homeostasis in murine liver.

altmetric score

  • 8.7

author list (cited authors)

  • Bond, L. M., Ibrahim, A., Lai, Z. W., Walzem, R. L., Bronson, R. T., Ilkayeva, O. R., Walther, T. C., & Farese, R. V.

citation count

  • 0

complete list of authors

  • Bond, Laura M||Ibrahim, Ayon||Lai, Zon W||Walzem, Rosemary L||Bronson, Roderick T||Ilkayeva, Olga R||Walther, Tobias C||Farese, Robert V

Book Title

  • bioRxiv

publication date

  • May 2022