Hepatocyte growth factor secreted by bone marrow stem cell reduce ER stress and improves repair in alveolar epithelial II cells

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作者
Izabela Nita
Katrin Hostettler
Luca Tamo
Michaela Medová
Giuseppe Bombaci
Jun Zhong
Ramanjaneyulu Allam
Yitzhak Zimmer
Michael Roth
Thomas Geiser
Amiq Gazdhar
机构
[1] University Hospital Bern,Department of Pulmonary Medicine
[2] Department of Clinical Research University of Bern,Department of Biomedicine
[3] Pulmonary Cell Research,Department of Radiation Oncology
[4] University and University Hospital Basel,Department of Hematology
[5] Graduate school of Biomedical science,undefined
[6] University of Bern,undefined
[7] Inselspital,undefined
[8] Bern University Hospital,undefined
[9] and University of Bern,undefined
[10] University Hospital Bern,undefined
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Scientific Reports | / 7卷
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摘要
Idiopathic Pulmonary Fibrosis (IPF) is a progressive, irreversible lung disease with complex pathophysiology. Evidence of endoplasmic reticulum (ER) stress has been reported in alveolar epithelial cells (AEC) in IPF patients. Secreted mediators from bone marrow stem cells (BMSC-cm) have regenerative properties. In this study we investigate the beneficial effects of BMSC-cm on ER stress response in primary AEC and ER stressed A549 cells. We hypothesize that BMSC-cm reduces ER stress. Primary AEC isolated from IPF patients were treated with BMSC-cm. To induce ER stress A549 cells were incubated with Tunicamycin or Thapsigargin and treated with BMSC-cm, or control media. Primary IPF-AEC had high Grp78 and CHOP gene expression, which was lowered after BMSC-cm treatment. Similar results were observed in ER stressed A549 cells. Alveolar epithelial repair increased in presence of BMSC-cm in ER stressed A549 cells. Hepatocyte growth factor (HGF) was detected in biologically relevant levels in BMSC-cm. Neutralization of HGF in BMSC-cm attenuated the beneficial effects of BMSC-cm including synthesis of surfactant protein C (SP-C) in primary AEC, indicating a crucial role of HGF in ER homeostasis and alveolar epithelial repair. Our data suggest that BMSC-cm may be a potential therapeutic option for treating pulmonary fibrosis.
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