scholarly journals TNF‐α/IL‐1β—licensed mesenchymal stromal cells promote corneal allograft survival via myeloid cell‐mediated induction of Foxp3 + regulatory T cells in the lung

2019 ◽  
Vol 33 (8) ◽  
pp. 9404-9421 ◽  
Author(s):  
Nick Murphy ◽  
Oliver Treacy ◽  
Kevin Lynch ◽  
Maurice Morcos ◽  
Paul Lohan ◽  
...  
2019 ◽  
Vol 103 (1) ◽  
pp. 182-190 ◽  
Author(s):  
Chunyi Shao ◽  
Yihe Chen ◽  
Takeshi Nakao ◽  
Afsaneh Amouzegar ◽  
Jia Yin ◽  
...  

2014 ◽  
Vol 12 (6) ◽  
pp. 708-718 ◽  
Author(s):  
Qiuli Liu ◽  
Haiqing Zheng ◽  
Xiaoyong Chen ◽  
Yanwen Peng ◽  
Weijun Huang ◽  
...  

2011 ◽  
Vol 19 ◽  
pp. S30-S31 ◽  
Author(s):  
S. Hagmann ◽  
B. Moradi ◽  
T. Müller ◽  
T. Dreher ◽  
S. Frank ◽  
...  

2021 ◽  
Author(s):  
Qianru Li ◽  
Jing Li ◽  
Lei Sun ◽  
Yun Sun ◽  
Fei Zhao ◽  
...  

Inflammatory response mediated by immune cells is either directly or indirectly regulated by mesenchymal stromal cells (MSCs). Accumulating evidence suggests that thrombospondin-1 (TSP-1) is highly expressed in response to inflammation. In this work, we isolated and identified human thymic mesenchymal stromal cells (tMSCs) and detected the expression of TSP-1. We found that tMSCs expressed TSP-1 and Poly (I: C) or LPS treatment promoted the expression of TSP-1. Further, we isolated and identified exosomes originating from tMSCs (MEXs). Notably, exosomes derived from LPS-pretreated tMSCs (MEXsLPS) promoted the polarization of macrophages to M1-like phenotype and IL-6, TNF-α secretion as well as the pro-inflammatory differentiation of CD4+T cells into Th17 cells. Upon silencing the expression of TSP-1 in tMSCs, the pro-inflammatory effects of MEXsLPS were suppressed. Therefore, these findings uncovered TSP-1 as the principal factor in MEXsLPS pro-inflammatory regulation.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Shang Li ◽  
Jing Yu ◽  
Chungang Guo ◽  
Ying Jie ◽  
Zhiqiang Pan

Purpose. CD4+LAP+ T cells are newly discovered regulatory T cells (Tregs). The aim of this study is to investigate the balance of Th1/Th2 and LAP+Tregs/Th17 in mice after allogeneic corneal transplantation. Methods. A total of 65 mice received orthotopic penetrating transplantation. According to the survival scores of the grafts, the mice were divided into the rejection group and the survival group 3 weeks after transplantation. Th1, Th2, Th17, and regulatory T cells in the ipsilateral drainage lymph nodes and spleens were measured with flow cytometry. The related cytokines in aqueous humor were also analyzed. Results. The frequencies of Foxp3+Tregs, GARP+Tregs, and LAP+Tregs in the survival group were significantly higher than those in the rejection group. And the expression trend of CD4+LAP+ T cells and CD4+GARP+ T cells was consistent. The level of IFN-γ, TNF, IL-6, and IL-17A markedly increased in aqueous humor during corneal allograft rejection. The ratio of Th1/Th2 and Th17/LAP+Tregs significantly increased in the rejection group at the 3rd week after corneal transplantation. Conclusion. LAP+Tregs might be regarded as substitute for Foxp3+Tregs. The balance of Th1/Th2 and LAP+Tregs/Th17 is crucial for corneal allograft survival.


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