Therapeutic effects of adipose-tissue-derived mesenchymal stromal cells and their extracellular vesicles in experimental silicosis

被引:50
作者
Bandeira, Elga [1 ,3 ]
Oliveira, Helena [1 ]
Silva, Johnatas D. [1 ]
Menna-Barreto, Rubem F. S. [2 ]
Takyia, Christina M. [1 ]
Suk, Jung S. [3 ]
Witwer, Kenneth W. [4 ,5 ]
Paulaitis, Michael E. [3 ]
Hanes, Justin [3 ]
Rocco, Patricia R. M. [1 ]
Morales, Marcelo M. [1 ,6 ]
机构
[1] Univ Fed Rio de Janeiro, Carlos Chagas Filho Biophys Inst, Rio De Janeiro, Brazil
[2] Fundacao Oswaldo Cruz, Oswaldo Cruz Inst, Rio De Janeiro, Brazil
[3] Johns Hopkins Univ, Sch Med, Ctr Nanomed, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Dept Mol & Comparat Pathobiol, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD USA
[6] Univ Fed Rio de Janeiro, Carlos Chagas Filho Inst Biophys, Lab Cellular & Mol Physiol, Ctr Ciencias Saude,Ilha Fundao, Ave Carlos Chagas Filho S-N,Bloco G1-55, BR-21941902 Rio De Janeiro, RJ, Brazil
来源
RESPIRATORY RESEARCH | 2018年 / 19卷
关键词
Silicosis; Mesenchymal stromal cells; Inflammation; Fibrosis; Extracellular vesicles; ACUTE LUNG INJURY; EXPERIMENTAL ALLERGIC-ASTHMA; BONE-MARROW; STEM-CELLS; MONONUCLEAR-CELLS; DRUG-DELIVERY; MICE; EXOSOMES; MICROVESICLES; BIODISTRIBUTION;
D O I
10.1186/s12931-018-0802-3
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Background: Silicosis is an occupational disease that affects workers who inhale silica particles, leading to extensive lung fibrosis and ultimately causing respiratory failure. Mesenchymal stromal cells (MSCs) have been shown to exert therapeutic effects in lung diseases and represent an alternative treatment for silicosis. Recently, it has been suggested that similar effects can be achieved by the therapeutic use of extracellular vesicles (EVs) obtained from MSCs. The aim of this study was to investigate the effects of adipose-tissue-derived MSCs (AD-MSCs) or their EVs in a model of silicosis. Methods: Silicosis was induced by intratracheal instillation of silica in C57BL/6 mice. After the onset of disease, animals received saline, AD-MSCs, or EVs, intratracheally. Results: At day 30, AD-MSCs and EVs led to a reduction in collagen fiber content, size of granuloma, and in the number of macrophages inside granuloma and in the alveolar septa. In addition, the expression levels of interleukin 1 beta and transforming growth factor beta in the lungs were decreased. Higher dose of EVs also reduced lung static elastance when compared with the untreated silicosis group. Conclusions: Both AD-MSCs and EVs, locally delivered, ameliorated fibrosis and inflammation, but dose-enhanced EVs yielded better therapeutic outcomes in this model of silicosis.
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页数:10
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