Angiopoietin-like protein 8 orchestrates macrophage glycogen metabolism and polarization via the JNK signaling pathway in cytokine storm syndrome
Yang Su, Rongtian Zhang, Kongdong Li, Hong Shen, Mengjiao Nan, Chang Liu, Wenxiang Zhang, Siyu Chen

TL;DR
This study shows that Angptl8 promotes harmful inflammation in a severe immune condition called cytokine storm syndrome and suggests it could be a new treatment target.
Contribution
The paper identifies Angptl8 as a novel regulator of macrophage polarization and glycogen metabolism via the JNK pathway in cytokine storm syndrome.
Findings
Angptl8 knockout reduces mortality in LPS-treated mice by inhibiting M1 macrophage activation.
Angptl8 promotes M1 macrophage polarization through JNK-mediated glycogen metabolism.
An Angptl8-neutralizing antibody improves CSS symptoms without toxicity in mice.
Abstract
Cytokine storm syndrome (CSS) is associated with severe damage and high mortality in acute diseases. Over-activation of M1 macrophages, accompanied with excessive pro-inflammatory cytokine secretion, drives cytokine storms, while promoting M2 macrophage polarization is a potential CSS treatment. The liver, an immune-responsive organ, secretes hepatokines such as fibroblast growth factor-21 (FGF-21) to regulate macrophage activation, but knowledge of their role in CSS-related inflammation is elusive, fueling the search for new hepatokines that can effectively fine-tune the pro-inflammatory activation of macrophages during CSS. In this study, lipopolysaccharide (LPS)-induced CSS signals increase hepatic Angiopoietin-like protein 8 (Angptl8) expression. Angptl8 knockout (Angptl8−/−) reduces mortality in high-dose LPS-treated mice. This is due to inhibited M1 and enhanced M2 macrophage…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7
Figure 8Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsLipid metabolism and disorders · Immune Cell Function and Interaction · Inflammasome and immune disorders
