Necroptosis is active and contributes to intestinal injury in a piglet model with lipopolysaccharide challenge

• Published in: Cell death & disease 2021-01, Vol.12 (1), p.62-62, Article 62
• Main Authors: Liu, Yulan, Xu, Qiao, Wang, Yang, Liang, Tianzeng, Li, Xiangen, Wang, Dan, Wang, Xiuying, Zhu, Huiling, Xiao, Kan
• Format: Article
• Language: English
• Subjects: 38; 38/1; 631/337/572; 631/80/82; Antibodies; Apoptosis; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell Culture; Cell death; Cytokines; Dynamin; HMGB1 protein; Immunology; Inflammation; Interleukin 6; Intestine; Jejunum; Kinases; Life Sciences; Lipopolysaccharides; Macrophages; MAP kinase; Mitochondria; Monocytes; Necroptosis; Phosphoglycerate mutase; Protein expression; Protein kinase; Proteins; Sepsis; Tumor necrosis factor-TNF; Tumor necrosis factor-α
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-020-03365-1

Necroptosis, a newly discovered form of programmed cell death that combines the features of apoptosis and necrosis, is important in various physiological and pathological disorders. However, the role of necroptosis on intestinal injury during sepsis has been rarely evaluated. This study aimed to investigate the presence of necroptosis in intestinal injury, and its contribution to intestinal injury in a piglet model challenged with Escherichia coli lipopolysaccharide (LPS). Firstly, a typical cell necrotic phenomenon was observed in jejunum of LPS-challenged pigs by transmission electron microscope. Protein expression of necroptosis signals including receptor-interacting protein kinase (RIP) 1, RIP3, and phosphorylated mixed-lineage kinase domain-like protein (MLKL), mitochondrial proteins including phosphoglycerate mutase family member 5 (PGAM5) and dynamin-related protein 1 (DRP1), and cytoplasmic high-mobility group box 1 (HMGB1) were time-independently increased in jejunum of LPS-challenged piglets, which was accompanied by the impairment of jejunal morphology, and digestive and barrier function indicated by lower activities of jejunal disaccharidases and protein expression of jejunal tight junction proteins claudin-1 and occludin. Pro-inflammatory cytokines including tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6 were also dynamically induced in serum and jejunum of piglets after LPS challenge. Moreover, pretreatment with necrostatin-1 (Nec-1), an specific inhibitor of necroptosis, inhibited necroptosis indicated by decreased necrotic ultrastructural changes and decreased protein expression of RIP1, RIP3, and phosphorylated MLKL as well as PGAM5, DRP1, and cytoplasmic HMGB1. Nec-1 pretreatment reduced jejunal morphological injury, and improved digestive and barrier function. Nec-1 pretreatment also decreased the levels of serum and jejunal pro-inflammatory cytokines and the numbers of jejunal macrophages and monocytes. These findings indicate for the first time that necroptosis is present and contributes to LPS-induced intestinal injury. Nec-1 may have a preventive effect on intestinal injury during sepsis.