Pendrin inhibition is associated with protective effect of prone positioning in a ventilator-induced lung injury mouse model

  • Sci Rep. 2025 Nov 20;15(1):40926. doi: 10.1038/s41598-025-24241-y.
Ji Soo Choi  1 Mi Hwa Shin  2  3 Go Eun Oh  2 Doo Na Song  4 Wan NamKung  5 Gyoon Hee Han  4  5 Jae Young Choi  3 Moo Suk Park  6
Affiliations
  • 1. Division of Pulmonology, Allergy and Critical Care Medicine, Department of Internal Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin-si, Gyeonggi-do, Republic of Korea.
  • 2. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-Ro, Seodaemun-Gu, Seoul, 03722, Republic of Korea.
  • 3. Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • 4. Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
  • 5. Department of Pharmacy, College of Pharmacy, Yonsei University, Incheon, 21983, Republic of Korea.
  • 6. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-Ro, Seodaemun-Gu, Seoul, 03722, Republic of Korea. [email protected].
Abstract

Pendrin (SLC26A4), a transmembrane anion exchanger, is upregulated in inflammatory airway diseases. In this study, we analyzed the role of pendrin expression in a ventilator-induced acute lung injury (VILI) animal model. VILI was induced in the supine or prone position by a high tidal volume (HTV) of 30 mL/kg for 5 h in pendrin wild-type (WT) and knockout (KO) 129SVEV mice. Pendrin inhibitor (YS-01) was intraperitoneally administered to modulate pendrin signaling. Lung injury parameters were assessed based on bronchoalveolar lavage fluid (BALF) analysis, inflammatory cytokine analysis by ELISA, and histopathological findings. Pendrin expression was determined by western blotting and transmission electron microscopy (TEM) using immunogold labeling methods. The degree of lung injury was significantly attenuated in pendrin-KO mice and pendrin-WT mice with YS-01 compared with pendrin-WT Animals after HTV ventilation. Pendrin expression was down-regulated in pendrin-KO mice and pendrin-WT mice with YS-01 compared with pendrin-WT mice with VILI, as determined by western blotting and TEM-immunogold labeling. Prone positioning during ventilation attenuated lung inflammation and pendrin expression. Our results suggest that pendrin is critical in VILI and could be a novel target for modulating VILI. Prone positioning and pendrin inhibition in VILI may be effective in managing these conditions.

Keywords
Acute lung injury; Acute respiratory distress syndrome; Pendrin; Prone; SLC26A4; ventilator-induced lung injury.
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