Adipose tissue-derived mesenchymal stromal cells attenuate acute lung injury induced by trauma and haemorrhagic shock

Immunobiology. 2023 Nov;228(6):152765. doi: 10.1016/j.imbio.2023.152765. Epub 2023 Nov 25.

Abstract

Background: Mesenchymal stromal cells (MSCs) have shown promising therapeutic options for acute lung injury (ALI) caused by multiple factors. Here, we evaluated the therapeutic potential of adipose tissue-derived mesenchymal stromal cells (ADSCs) in trauma and hemorrhagic shock (THS)-induced ALI.

Methods: ALI model induced by THS was constructed by fractures plus abdominal trauma plus acute hemorrhage plus fluid resuscitation. The ADSCs group rats were generated by injecting 2 × 106 ADSCs at 0 and 1 h after THS. The sham, ALI, and ADSCs group rats were sacrificed at 24 h after resuscitation. The changes in lung histopathology, total protein in bronchoalveolar lavage fluid (BALF), mRNA expression of pro-inflammatory/anti-inflammatory cytokines, antioxidant, and anti-apoptotic indicator, and the activity of Toll-like receptor 4 (TLR4) signaling in lung tissues were evaluated.

Results: Administration of the ADSCs reversed ALI induced by THS, including lung histopathological changes/scores, and BALF total protein concentration. Additionally, ADSCs therapy also significantly down-regulated mRNA expression of pro-inflammatory TNF-α, IL-1β, and IL-6, up-regulated mRNA expression of anti-inflammatory IL-10, anti-apoptotic molecule Bcl-2, and anti-oxidative molecule HO-1 in THS rats. Furthermore, ADSCs suppressed the expression of TLR4 in lung tissue.

Conclusion: Our data show that ADSCs administration can exert therapeutic effects on THS-induced ALI in rats and may provide beneficial in preventative strategies for ALI.

Keywords: Acute lung injury; Adipose tissue-derived mesenchymal stromal cells; Inflammation; Trauma and haemorrhagic shock.

MeSH terms

  • Acute Lung Injury* / etiology
  • Acute Lung Injury* / therapy
  • Animals
  • Anti-Inflammatory Agents
  • Lung / pathology
  • Mesenchymal Stem Cells* / metabolism
  • RNA, Messenger
  • Rats
  • Shock, Hemorrhagic* / complications
  • Shock, Hemorrhagic* / therapy
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / metabolism

Substances

  • Toll-Like Receptor 4
  • Anti-Inflammatory Agents
  • RNA, Messenger