The Clinical Value of GDF15 and Its Prospective Mechanism in Sepsis

Front Immunol. 2021 Sep 8:12:710977. doi: 10.3389/fimmu.2021.710977. eCollection 2021.

Abstract

Growth differentiation factor 15 (GDF15) is involved in the occurrence and development of many diseases, and there are few studies on its relationship with sepsis. This article aims to explore the clinical value of GDF15 in sepsis and to preliminarily explore its prospective regulatory effect on macrophage inflammation and its functions. We recruited 320 subjects (132 cases in sepsis group, 93 cases in nonsepsis group, and 95 cases in control group), then detected the serum GDF15 levels and laboratory indicators, and further investigated the correlation between GDF15 and laboratory indicators, and also analyzed the clinical value of GDF15 in sepsis diagnosis, severity assessment, and prognosis. In vitro, we used LPS to stimulate THP-1 and RAW264.7 cells to establish the inflammatory model, and detected the expression of GDF15 in the culture medium and cells under the inflammatory state. After that, we added GDF15 recombinant protein (rGDF15) pretreatment to explore its prospective regulatory effect on macrophage inflammation and its functions. The results showed that the serum GDF15 levels were significantly increased in the sepsis group, which was correlated with laboratory indexes of organ damage, coagulation indexes, inflammatory factors, and SOFA score. GDF15 also has a high AUC in the diagnosis of sepsis, which can be further improved by combining with other indicators. The dynamic monitoring of GDF15 levels can play an important role in the judgment and prognosis of sepsis. In the inflammatory state, the expression of intracellular and extracellular GDF15 increased. GDF15 can reduce the levels of cytokines, inhibit M1 polarization induced by LPS, and promote M2 polarization. Moreover, GDF15 also enhances the phagocytosis and bactericidal function of macrophages. Finally, we observed a decreased level of the phosphorylation of JAK1/STAT3 signaling pathway and the nuclear translocation of NF-κB p65 with the pretreatment of rGDF15. In summary, our study found that GDF15 has good clinical application value in sepsis and plays a protective role in the development of sepsis by regulating the functions of macrophages and inhibiting the activation of JAK1/STAT3 pathway and nuclear translocation of NF-κB p65.

Keywords: GDF15; JAK1/STAT3; NF-κB p65; biomarker; inflammation; macrophage polarization; phagocytosis and sterilization; sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Female
  • Growth Differentiation Factor 15 / blood
  • Growth Differentiation Factor 15 / physiology*
  • Humans
  • Janus Kinase 1 / physiology
  • Macrophages / immunology
  • Male
  • Mice
  • Middle Aged
  • Prognosis
  • RAW 264.7 Cells
  • STAT3 Transcription Factor / physiology
  • Sepsis / blood
  • Sepsis / diagnosis
  • Sepsis / etiology*
  • Sepsis / mortality
  • Severity of Illness Index
  • Shock, Septic / diagnosis
  • Signal Transduction
  • THP-1 Cells
  • Transcription Factor RelA / metabolism

Substances

  • GDF15 protein, human
  • Growth Differentiation Factor 15
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Transcription Factor RelA
  • JAK1 protein, human
  • Janus Kinase 1