Search bioRxiv⌕ Search

Biology subjects

Cybulsky, M.

Publications and source records attributed to Cybulsky, M..

2 recordsLinked to original sources

Cholesterol accumulation-induced impairment of AKT signaling in LPS-stimulated macrophages play a dispensable role in suppressing HIF-1α-dependent glycolysis

The formation of lipid-laden macrophages (M{varphi}s) is a hallmark of atherosclerosis, yet how the accumulation of cholesterol in M{varphi}s underlies the inflammatory process of atherogenesis remains unclear. It is well recognized that the reprogramming of metabolism in M{varphi}s is critical for supporting their inflammatory responses, which may shed light on how the metabolism of M{varphi} foam cells is linked to inflammation. Indeed, recent research has now revealed M{varphi}s that accumulate excess cholesterol adopt a distinct metabolic adaptation, a metabolic profile that is unexpectedly associated with a deactivated inflammatory response. Mechanistically, our group has previously shown that upon LPS stimulation, excess cholesterol accumulation in M{varphi}s impaired their induction of AKT-dependent early glycolytic reprogramming and HIF-1-dependent late glycolytic reprogramming. However, it remains unclear if these events are interconnected and synergistically contribute to the suppression of inflammation observed in these M{varphi}s. Here, we demonstrated that cholesterol loading of M{varphi}s impaired LPS-induced early glycolysis by reducing the phosphorylation of hexokinases, yet complete inhibition of AKT only modestly impaired HIF-1-dependent glycolytic reprogramming. On the other hand, we confirmed that HIF-1 degradation, but not its reduced synthesis, is the primary mechanism that underlies its impaired expression in cholesterol loaded M{varphi}s. Finally, we showed that cholesterol loading of M{varphi}s alone was sufficient to induce oxidative stress, such as the production of 4-HNE, and deplete the levels of reduced KEAP1 proteins. M{varphi}s lacking NRF2 resisted the effects of cholesterol loading on suppressing the expression of glycolytic and pro-inflammatory proteins.

immunology↗

Intracellular accumulation of free cholesterol in macrophages triggers a PARP1 response to DNA damage and PARP1 impairs lipopolysaccharide-induced inflammatory response

The formation of macrophage (M{varphi}) foam cells is a hallmark of atherosclerosis, yet how the process of lipid loading can modulate M{varphi} inflammatory responses by rewiring their intracellular metabolic circuits is not well understood. Our previous studies have shown that the accumulation of oxidized LDL (oxLDL) or free cholesterol in M{varphi}s impaired their inflammatory response by suppressing HIF-1-mediated glycolysis and upregulating NRF2 antioxidative response. However, it remains unclear if other metabolic processes are also contributory. In this study, we found that the accumulation of free cholesterol, but not oxLDL, in primary murine thioglycolate-elicited peritoneal M{varphi}s (PM{varphi}s) enhanced a PARP1-dependent response associated with repair of DNA damage, which was characterized by poly ADP-ribosylation of proteins, phosphorylation of histone 2A.X and consumption of NAD+. Both oxLDL and cholesterol enhanced the PARP1 response after LPS stimulation. Treatment of PM{varphi}s with mitoTEMPO, a specific mitochondrial reactive oxygen species (mtROS) scavenger, alleviated mtROS during cholesterol loading, blocked the PARP1 response and partially restored LPS-induced inflammatory gene expression. In contrast to inhibition of PARP1 enzymatic activity, knockdown of PARP1 expression in RAW264.7 M{varphi}s with siRNA elevated LPS-induced inflammatory gene expression. Overall, our study suggests that cholesterol accumulation triggers a PARP1 response to DNA damage in M{varphi}s and that PARP1 inhibits LPS-mediated inflammation through a non-enzymatic function.

immunology↗