miR‑4792 regulates inflammatory responses in Cryptococcus neoformans‑infected microglia

Guotai Yao1, Xiaoli Wang1, Yan Wang1

  • 1Department of Dermatology, Changzheng Hospital, Naval Medical University, Shanghai 200003, P.R. China.

Insights

MicroRNA-4792 (miR-4792) is downregulated in cryptococcal meningitis (CM), leading to increased inflammation. Restoring miR-4792 levels may offer a therapeutic strategy for CM.

Area of Science:

  • Immunology
  • Neuroscience
  • Microbiology

Background:

  • Microglial cells are key in cryptococcal meningitis (CM) pathogenesis.
  • MicroRNAs (miRNAs) regulate immune responses during infection, but their role in CM is unclear.
  • Previous work profiled miRNAs in THP-1 cells post-Cryptococcus neoformans infection.

Purpose of the Study:

  • To investigate the role of miR-4792 in the inflammatory response during CM.
  • To identify potential diagnostic markers for CM.

Main Methods:

  • Assessed miR-4792 and epidermal growth factor receptor (EGFR) expression in C. neoformans-infected BV2 cells.
  • Overexpressed miR-4792 in infected cells to observe effects on EGFR, MAPK signaling, and cytokine secretion.
  • Analyzed miR-4792 and EGFR levels in cerebrospinal fluid from CM patients.
  • Performed receiver operator characteristic (ROC) analysis for diagnostic potential.

Main Results:

  • miR-4792 was downregulated, and EGFR was upregulated in C. neoformans-infected BV2 cells.
  • miR-4792 overexpression reduced EGFR expression, MAPK signaling, and inflammatory cytokine secretion.
  • In CM patients, miR-4792 levels increased, and EGFR levels decreased after antifungal treatment.
  • ROC analysis indicated miR-4792 (AUC=0.75) and EGFR (AUC=0.79) as potential diagnostic markers.

Conclusions:

  • miR-4792 plays a regulatory role in microglial inflammatory responses to C. neoformans.
  • EGFR is a target of miR-4792 and is involved in CM pathogenesis.
  • miR-4792 and EGFR show potential as diagnostic biomarkers for cryptococcal meningitis.