Abstract | OBJECTIVES: MATERIALS AND METHODS: Mouse and human DASCs were expanded, analysed, and engrafted into injured mouse lungs. Single-cell analyses were performed to reveal the differentiation path of the engrafted cells. Finally, human DASCs were transplanted into COPD mice induced by porcine pancreatic elastase (PPE) and lipopolysaccharide (LPS) administration. RESULTS: We showed that isolated mouse and human DASCs could be indefinitely expanded and were able to further differentiate into mature alveolar structures in vitro. Single-cell analysis indicated that the engrafted cells expressed typical cellular markers of type I alveolar cells as well as the specific secreted proteins. Interestingly, transplantation of human DASCs derived from COPD patients into the lungs of NOD-SCID mice with COPD injury repaired the tissue damage and improved the pulmonary function. CONCLUSIONS:
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Authors | Xiaofan Wang, Yu Zhao, Dandan Li, Yun Feng, Yusang Xie, Yueqing Zhou, Min Zhou, Yujia Wang, Jieming Qu, Wei Zuo |
Journal | Cell proliferation
(Cell Prolif)
Vol. 54
Issue 6
Pg. e13046
(Jun 2021)
ISSN: 1365-2184 [Electronic] England |
PMID | 33960563
(Publication Type: Journal Article)
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Copyright | © 2021 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. |
Topics |
- Animals
- Female
- Heterografts
- Humans
- Lung
(metabolism, pathology)
- Male
- Mice
- Mice, Inbred NOD
- Mice, SCID
- Pulmonary Disease, Chronic Obstructive
(metabolism, pathology, therapy)
- Stem Cell Transplantation
- Stem Cells
(metabolism, pathology)
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