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SIRT1 relieves Necrotizing Enterocolitis through inactivation of Hypoxia-inducible factor (HIF)-1a

Ming Bai, Chaoxiang Lu, Lu An, Qi Gao, Weike Xie, Feng Miao, Xiaofeng Chen, Yongkang Pan, Qi Wang

2020Cell Cycle34 citationsDOIOpen Access PDF

Abstract

model was established by using LPS-induced NEC-like cell in this study. The results indicate that overexpression of SIRT1 inhibited the cell apoptosis induced by LPS. Besides, overexpression of SIRT1 suppressed the high expression of proinflammatory factors (IL-6, IL-8, and TNF-α), the decrease of transepithelial electrical resistance (TEER), and the decline expression of tight junction proteins (ZO-1, ZO-2, and Claudin-4) induced by LPS in Caco-2 cells. What is more, serum HIF-1α was increased in NEC patients. SIRT1 overexpression suppressed the expression and activity of HIF-1a, while knockdown of SIRT1 made the opposite effect. In summary, this study indicates that overexpression of SIRT1 alleviates the inflammation response and intestinal epithelial barrier dysfunction through regulating the expression and inactivation of HIF-1a.

Topics & Concepts

Necrotizing enterocolitisApoptosisSirtuin 1BiologyProinflammatory cytokineInflammationTumor necrosis factor alphaGene knockdownHypoxia (environmental)Cancer researchProgrammed cell deathHypoxia-inducible factorsImmunologyNecrosisDownregulation and upregulationInternal medicineMedicineChemistryBiochemistryGeneOxygenGeneticsOrganic chemistrySirtuins and Resveratrol in MedicineAdenosine and Purinergic SignalingCytomegalovirus and herpesvirus research
SIRT1 relieves Necrotizing Enterocolitis through inactivation of Hypoxia-inducible factor (HIF)-1a | Litcius