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Platelet Exosome-Derived miR-223-3p Regulates Pyroptosis in the Cell Model of Sepsis-Induced Acute Renal Injury by Targeting Mediates NLRP3.
Wan, Peng; Tan, Xiang; Sheng, Mengting; Xiang, Yan; Wang, Peng; Yu, Min.
Afiliación
  • Wan P; Department of Critical Care Medicine, The First Clinical Medical College of Three Gorges University,Yichang Central People's Hospital, Yichang City, Hubei, 443000, China.
  • Tan X; Department of Critical Care Medicine, The First Clinical Medical College of Three Gorges University,Yichang Central People's Hospital, Yichang City, Hubei, 443000, China.
  • Sheng M; Department of Critical Care Medicine, The First Clinical Medical College of Three Gorges University,Yichang Central People's Hospital, Yichang City, Hubei, 443000, China.
  • Xiang Y; Department of Critical Care Medicine, The First Clinical Medical College of Three Gorges University,Yichang Central People's Hospital, Yichang City, Hubei, 443000, China.
  • Wang P; Department of Critical Care Medicine, The First Clinical Medical College of Three Gorges University,Yichang Central People's Hospital, Yichang City, Hubei, 443000, China.
  • Yu M; The people's hospital of China Three Gorges University.
Crit Rev Immunol ; 44(3): 53-65, 2024.
Article en En | MEDLINE | ID: mdl-38421705
ABSTRACT

BACKGROUND:

The present study investigated the roles and mechanisms of platelet-derived exosomes in sepsis-induced acute renal injury.

METHODS:

The blood samples of septic patients and healthy controls were collected for clinical examination. The plasma levels of miR-223-3p and NLRP3 mRNA were analyzed by qRT-PCR and the serum IL-1ß and creatinine levels were quantified by enzyme-linked immunosorbent assay (ELISA). C57BL/6 mice injected with LPS (lipopolysaccharide) were employed as the animal model for sepsis-induced acute renal injury. Human coronary artery endothelial cells (HCAECs) were treated with TNF-α as a cellular model for sepsis-induced endothelial damages.

RESULTS:

The number of PMP (platelet-derived microparticles) in patients with sepsis was increased. The level of miR-223-3p in the platelet exosomes isolated from the serum sample in patients with sepsis was significantly lower than that of the healthy controls. The level of miR-223-3p was also decreased in the platelet exosomes of mouse model with sepsis-induced acute renal injury. Downregulating miR-223-3p promoted sepsis-induced acute renal injury in mice model, while the administration of miR-223-3p reduced the inflammation in endothelial cells of sepsis-induced acute renal injury. NLRP3 (NLR Family Pyrin Domain Containing 3) was identified as one target of miR-223-3p in the platelet exosomes of sepsis-induced acute kidney injury. miR-223-3p attenuated NLRP3-induced pyroptosis in endothelial cell model of sepsis-induced acute kidney injury.

CONCLUSION:

Our data suggest that platelet exosome-derived miR-223-3p negatively regulates NLRP3-dependent inflammasome to suppress pyroptosis in endothelial cells. Decreased miR-223-3p expression promotes the inflammation in sepsis-induced acute renal injury. Targeting miR-223-3p may be developed into a therapeutic approach for sepsis-induced acute renal injury.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sepsis / MicroARNs / Micropartículas Derivadas de Células / Exosomas / Lesión Renal Aguda Límite: Animals / Humans Idioma: En Revista: Crit Rev Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sepsis / MicroARNs / Micropartículas Derivadas de Células / Exosomas / Lesión Renal Aguda Límite: Animals / Humans Idioma: En Revista: Crit Rev Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China