陆军军医大学学报 (Jul 2024)

Role of Fgl2 in macrophage polarization during acute kidney injury in mice

  • ZHU Lin,
  • XU Guilian,
  • XIE Pan

DOI
https://doi.org/10.16016/j.2097-0927.202401019
Journal volume & issue
Vol. 46, no. 13
pp. 1467 – 1476

Abstract

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Objective To investigate the role of fibrinogen-like protein 2 (Fgl2) in macrophage polarization during cisplatin (Cis)-induced acute kidney injury (Cis-AKI). Methods Twelve male wild-type (Fgl2+/+) mice and 12 Fgl2 gene knockout (Fgl2-/-) mice, aged 8~10 weeks and weighing 20~25 g, were selected, and then after being administered with a single intraperitoneal injection of either saline or Cis for 3 d, they were randomly divided into 4 groups (n=6): Fgl2+/+ Saline group, Fgl2+/+ Cis group, Fgl2-/- Saline group and Fgl2-/- Cis group. Kidney function indicators such as serum creatinine (Scr) and blood urea nitrogen (BUN) levels were measured 3 d later, and kidney injury was assessed by HE staining. Western blot analysis was performed to evaluate the expression of Fgl2 and kidney injury molecule 1 (Kim-1) in the renal tissues. RT-qPCR was conducted to assess the expression levels of Fgl2, Kim-1, neutrophil gelatinase-associated lipocalin (NGAL), IL-6, IL-12p40, IL-1β, inducible nitric oxide synthase (iNOS) and TNF-α in the renal tissues. Immunohistochemical assay was employed to detect the expression of Fgl2 and macrophages (F4/80+) in the kidneys. Immunofluorescence staining was utilized to examine the expression of macrophages (F4/80+) and M1-type macrophages (F4/80+CD86+) in the renal tissues. Flow cytometry was employed to analyze the expression of macrophages (F4/80+) as well as M1-type macrophages (F4/80+MHC Ⅱ+) and M2-type macrophages (F4/80+CD206+) in the renal tissues. Results Compared with the Fgl2+/+ Saline group, the Fgl2+/+ Cis group exhibited a significant decline in renal function (P < 0.05), a notable increase in pathological score of renal tubular injury (P < 0.05), and an obvious upregulation of renal tissue Fgl2 expression (P < 0.05). Compared with the Fgl2+/+ Cis group, the Fgl2-/- Cis group demonstrated a significant decline in renal function (P < 0.05), an elevation in the expression of renal injury-associated molecules Kim-1 and NGAL (P < 0.05), an increase in pathological score of renal tubular injury (P < 0.05), increase in macrophage infiltration (P < 0.05), and an upregulation in the expression of M1-type macrophage-related molecules IL-6, IL-1β, TNF-α and iNOS (P < 0.05), as well as obviously increase in the percentage of M1-type macrophages as indicated by flow cytometry (P < 0.05), while there was no significant change in the percentage of M2-type macrophages, and the proportion of M1-type macrophages was significantly higher than that of M2-type macrophages (P < 0.05). Conclusion Fgl2 gene knockout exacerbates Cis-AKI by promoting macrophage polarization towards the M1 phenotype.

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