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Table of Contents
Vol. 27, No. 5, 2011
Issue release date: June 2011
Section title: Original Paper
Cell Physiol Biochem 2011;27:587–596

Intrapulmonary Delivery of Human Umbilical Cord Mesenchymal Stem Cells Attenuates Acute Lung Injury by Expanding CD4+CD25+ Forkhead Boxp3 (FOXP3) + Regulatory T Cells and Balancing Anti- and Pro-inflammatory Factors

Sun J.1 · Han Z.-B.1,2 · Liao W.1 · Yang S.G.1 · Yang Z.X.1 · Yu J.X.1 · Meng L.1 · Wu R.3 · Han Z.C.1,2
1The State key Laboratory of Experimental Hematology, National Engineering Technology Research Center of Stem Cells, Institute of Hematology and Hospital of Blood Diseases, Chinese Academy of Medical Sciences and Peking Union of Medical College Tsinghua university, Tianjin;2National Engineering Research Center of Cell Products, AmCellGene Co. Ltd, Tianjin;3Department of Pediatrics, the Hospital of HuaiAn, Jiangsu Province, China
email Corresponding Author

Prof. Zhong Chao Han

The State key Laboratory of Experimental Hematology, Institute of Hematology

and Hospital of Blood Diseases, 288 Nanjing Road, Tianjin 300020 (China)

Tel. +86 22 66211430, Fax +86 22 66211430; E-Mail hanzhongchao@hotmail.com

or E-Mail sunjun2008387@gmail.com (Jun Sun)

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Background: Systemic and local inflammatory processes play key, mainly detrimental roles in the pathophysiology of acute lung injury (ALI). The present study was designed to determine whether human umbilical cord mesenchymal stem cells (UCMSC) are able to act on CD4+CD25+ Foxp3+Treg cells and lead to an improvement in ALI. Methods: Mice were administered intratracheally endotoxin (lipopolysaccharide [LPS]) and received intrapulmonary 1×106 UCMSC 4 hours after challenge. The CD4+CD25+ Foxp3+Treg, survival time, body weight, histology and lung injury scores were assessed after transplantation of UCMSC. In addition, anti-inflammatory factor IL10 and pro-inflammatory mediators production including tumor necrosis factor-a (TNF-α), macrophage inflammatory protein-2(MIP-2) and interferon-γ (IFN-γ) were detected. Results: Transplantation of UCMSC resulted in significant increase in the level of CD4+CD25+ Foxp3+Treg in ALI. Increased level of anti-inflammatory factor IL-10 and reduced levels of TNF-α, MIP-2 and IFN-γ were simultaneously observed in ALI in comparison with control mice. Conclusion: Our data demonstrate for the first time that transplantation of UCMSC ameliorates ALI by enhancing the diminished levels of alveolar CD4+CD25+ Foxp3+Treg and balancing anti- and pro-inflammatory factors in ALI mice.

© 2011 S. Karger AG, Basel

Article / Publication Details

First-Page Preview
Abstract of Original Paper

Accepted: April 27, 2011
Published online: June 15, 2011
Issue release date: June 2011

ISSN: 1015-8987 (Print)
eISSN: 1421-9778 (Online)

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