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Related Concept Videos

Acute Inflammation II: Cellular Phase01:26

Acute Inflammation II: Cellular Phase

The cellular phase of acute inflammation is a tightly orchestrated sequence of events that recruits leukocytes, primarily neutrophils, to sites of tissue injury or infection. Following the initial vascular changes, this phase ensures effective immune cell migration, activation, and function at the affected site to eliminate pathogens and initiate tissue repair.Leukocyte Recruitment CascadeLeukocyte recruitment happens in four steps: margination, adhesion, transmigration, and chemotaxis. Reduced...

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Related Experiment Video

Updated: Jun 29, 2026

Glycomics-Guided Glycoproteomics Facilitates Comprehensive Profiling of the Glycoproteome in Complex Tumor Microenvironments
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lncRNA-mRNA Co-expression Network Unveils Neutrophil Metabolic Reprogramming in Human Sepsis.

Peng Zhang1,2, Fupeng Wang1, Kang Zhao3

  • 1Department of Critical Care Medicine, Department of Transfusion Medicine, Daping Hospital, State Key Laboratory of Trauma and Chemical Poisoning, Army Medical University, Chongqing, 400042, China.

Inflammation
|June 3, 2026
PubMed
Summary
This summary is machine-generated.

Sepsis alters neutrophil metabolism. This study identifies long non-coding RNAs (lncRNAs) regulating amino acid metabolism in neutrophils during sepsis, offering new therapeutic targets.

Keywords:
MetabolismNeutrophilSepsislncRNAs

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Area of Science:

  • Immunology
  • Molecular Biology
  • Metabolomics

Background:

  • Sepsis involves immune dysregulation and metabolic changes in immune cells.
  • Neutrophils are key players in sepsis, adapting their metabolism for effector functions.
  • Long non-coding RNAs (lncRNAs) influence sepsis progression and metabolic reprogramming.

Purpose of the Study:

  • To investigate the interplay between lncRNAs and metabolic reprogramming in neutrophils during sepsis.
  • To identify specific lncRNAs and metabolic pathways involved in neutrophil dysfunction in sepsis.

Main Methods:

  • RNA sequencing was performed on neutrophils isolated from septic patients.
  • Bioinformatic analysis was used to identify differentially expressed genes and lncRNA networks.
  • Co-expression network analysis was employed to uncover regulatory relationships.

Main Results:

  • A set of hub differentially expressed genes related to amino acid metabolism was identified in septic neutrophils.
  • Potential lncRNA networks regulating these metabolic genes were uncovered.
  • The study revealed a broader landscape of neutrophil metabolic reprogramming in sepsis.

Conclusions:

  • lncRNAs play a significant role in regulating amino acid metabolism in neutrophils during sepsis.
  • The findings provide a foundational co-expression network for future research.
  • This work opens new avenues for understanding and targeting lncRNA-mediated metabolic alterations in sepsis.