Effects of Human Umbilical Cord-Derived Mesenchymal Stem Cells on the Acute Cigarette Smoke-Induced Pulmonary Inflammation Model
Journal
Frontiers in Physiology
Journal Volume
11
Date Issued
2020
Author(s)
Chen, X.-Y.
Chen, Y.-Y.
Lin, W.
Chien, C.-W.
Chen, C.-H.
Wen, Y.-C.
Hsiao, T.-C.
Chuang, H.-C.
Abstract
Cigarette smoke (CS) has been reported to induce oxidative stress and inflammatory process in the lungs. However, the role of human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) in the regulation of pulmonary inflammation remains unclear. The objective of this study is to investigate the effects of hUC-MSCs on lung inflammation in the acute CS-induced pulmonary inflammation animal model. Eight-week-old male C57BL/6 mice were intravenously administered 3 × 106, 1 × 107, and 3 × 107 cells/kg of hUC-MSCs as well as normal saline alone (control) after 3 days of CS exposure. Mice exposed to high-efficiency particulate air (HEPA)-filtered room air served as the CS control group. High-dose (3 × 107 cells/kg) hUC-MSC administration significantly decreased tumor necrosis factor (TNF)-α in the bronchoalveolar lavage fluid (BALF) of CS-exposed mice (p < 0.05). The chemokine (CXC motif) ligand 1/keratinocyte chemoattractant (CXCL1/KC) in BALF were significantly reduced by low-dose (3 × 106 cells/kg) and high-dose (3 × 107 cells/kg) hUC-MSC (p < 0.05). Medium-dose hUC-MSC administration decreased interleukin (IL)-1β in lung of mice, and TNF-α and caspase-3 were decreased in the lung of CS-exposed mice by medium- and high-dose MSC (p < 0.05). Low-dose hUC-MSCs significantly elevated serum CXCL1/KC and IL-1β in CS-exposed mice (p < 0.05). Our results suggest that high-dose hUC-MSCs reduced pulmonary inflammation and had antiapoptotic effects in acute pulmonary inflammation. ? Copyright ? 2020 Chen, Chen, Lin, Chien, Chen, Wen, Hsiao and Chuang.
Subjects
cigarette smoke; inflammation; lung; mesenchymal stem cells; oxidative stress
SDGs
Other Subjects
caspase 3; CXCL1 chemokine; interleukin 1beta; tumor necrosis factor; acute disease; animal experiment; animal model; animal tissue; antiapoptotic activity; Article; body weight; bronchoalveolar lavage fluid; C57BL 6 mouse; cigarette smoking; controlled study; enzyme linked immunosorbent assay; human; human cell; lung injury; lung parenchyma; male; mesenchymal stem cell transplantation; mouse; nonhuman; particulate matter; pneumonia; protein motif; therapy effect; umbilical cord
Type
journal article