CREBH Systemically Regulates Lipid Metabolism by Modulating and Integrating Cellular Functions

Abstract

Cyclic AMP-responsive element-binding protein H (CREBH, encoded by CREB3L3) is a membrane-bound transcriptional factor expressed in the liver and small intestine. The activity of CREBH is regulated not only at the transcriptional level but also at the posttranslational level. CREBH governs triglyceride metabolism in the liver by controlling gene expression, with effects including the oxidation of fatty acids, lipophagy, and the expression of apolipoproteins related to the lipoprotein lipase activation and suppression of lipogenesis. The activation and functions of CREBH are controlled in response to the circadian rhythm. On the other hand, intestinal CREBH downregulates the absorption of lipids from the diet. CREBH deficiency in mice leads to severe hypertriglyceridemia and fatty liver in the fasted state and while feeding a high-fat diet. Therefore, when crossing CREBH knockout (KO) mice with an atherosclerosis model, low-density lipoprotein receptor KO mice, these mice exhibit severe atherosclerosis. This phenotype is seen in both liver- and small intestine-specific CREBH KO mice, suggesting that CREBH controls lipid homeostasis in an enterohepatic interaction. This review highlights that CREBH has a crucial role in systemic lipid homeostasis to integrate cellular functions related to lipid metabolism.

Integrative analysis of the transcriptome and metabolome reveals the importance of hepatokine FGF21 in liver aging

“…2 I). Creb3l3, Mysm1, and Bach1, which are aging-related TFs, 41 , 42 , 43 were strongly correlated with the peroxisome pathway ( Fig. 2 I).…”

“…Creb3l3 regulates lipophagy, the oxidation of fatty acids, and the expression of apolipoproteins to maintain the homeostasis of lipid metabolism by governing related gene expression. 43 Notably, fatty acid accumulation can trigger aging of the liver. 12 Hence, Creb3l3 is an important TF worth further research.…”

FACI is a novel clathrin adaptor protein 2-binding protein that facilitates low-density lipoprotein endocytosis

“…Proprotein convertase subtilisin/kexin type 9 (PCSK9) binds to the LDLR at the cell surface and redirects it into lysosome for degradation [ 15 , 16 ]. E3 ubiquitin ligase inducible degrader of the LDL receptor (IDOL) catalyzes LDLR ubiquitylation and mediates its degradation [ 17 ].cAMP-responsive element-binding protein H (CREB-H) is a liver- and intestine-enriched transcription factor, which plays an important role in lipid metabolism [ 18 , 19 ]. CREB-H knockout (CREB-H −/− ) mice showed dyslipidemia and impaired lipoprotein clearance by livers [ 20 , 21 ].…”