ASIC1a induces mitochondrial apoptotic responses in acute lung injury

Aim: This study aimed to investigate the promoting effect of acid-sensing ion channel 1a (ASIC1a) on lipo-polysaccharide (LPS)-induced acute lung injury (ALI) and its mechanisms. Methods: In this experiment, the ALI rat model was induced by intratracheal injection of LPS, and the ASIC1a specific blocker psalmotoxin-1 (PcTx-1) was injected into the tail vein before LPS administration once. Western blot, immunofluorescence, immuno-histochemistry and real-time PCR methods were used to detect ASIC1a and apoptosis-related proteins expres-sions in lung tissue and RLE-6TN rat type II alveolar epithelial cells. Confocal Laser Scanning Microscopy was used to detect Ca2+ fluorescence intensity in RLE-6TN cells. Results: PcTx-1 pretreatment not only inhibited the pathological changes of LPS-induced ALI in lung tissue, but also inhibited lung dysfunction. PcTx-1 also reduced the increased levels of the apoptosis-related proteins B-cell lymphoma-2-associated X (Bax) and cleaved cysteinyl aspartate specific proteinase 3 (Cleaved caspase-3) and increased the decreased level of B-cell lymphoma-2 (Bcl-2) in the lung tissue of the model group. LPS-induced changes in mitochondrial membrane potential and calcium influx in alveolar epithelial cells were also reversed by PcTx-1. Conclusion: ASIC1a induces an apoptotic response in ALI through mitochondrial apoptosis.

Automated summary

In this study, the researchers investigated the promoting effect of ASIC1a on LPS-induced ALI and its mechanisms. They found that ASIC1a induces apoptotic response in ALI through mitochondrial apoptosis. Pretreatment with the ASIC1a specific blocker PcTx-1 inhibited both the pathological changes of ALI and lung dysfunction. PcTx-1 also reduced the expression of apoptosis-related proteins and reversed the changes in mitochondrial membrane potential and calcium influx.