Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes
Mesenchymal stromal cells (MSCs) based therapy is a promising approach to treat inflammatory disorders. However, therapeutic effect is not always achieved. Thus the mechanism involved in inflammation requires further elucidation. To explore the mechanisms by which MSCs respond to inflammatory stimul...
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doaj-9c00e9f3ce89432fbb177d22cac5b95c2020-11-25T01:56:46ZengElsevierEBioMedicine2352-39642018-06-01323142Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 InflammasomesYaozhen Chen0Xiangyang Qin1Qunxing An2Jing Yi3Fan Feng4Dandan Yin5Ning An6Zheng Liu7Lihong Weng8Shouwen Chen9Xingbin Hu10Wen Yin11Department of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, China; Department of Microbiology, School of Basic Medicine, Fourth Military Medical University, Xi'an, Shaanxi 710032, ChinaDepartment of Chemistry, School of Pharmacy, Fourth Military Medical University, Xi'an, Shaanxi 710032, ChinaDepartment of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, ChinaDepartment of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, ChinaDivision of Digestive Surgery, Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, Shaanxi 710032, ChinaDepartment of Hematology, Tangdu Hospital, Fourth Military Medical University, Xi'an 710032, ChinaDepartment of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, ChinaDepartment of Biochemistry and Molecular Biophysics, Columbia University, NewYork 10032, USADepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte 91010, CA, USAState Key Laboratory of Bioreactor Engineering, East China University of Science and technology, Shanghai 200237, ChinaDepartment of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, China; Corresponding authors at: Department of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, China.Department of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, China; Department of Microbiology, School of Basic Medicine, Fourth Military Medical University, Xi'an, Shaanxi 710032, China; Corresponding authors at: Department of Transfusion Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, China.Mesenchymal stromal cells (MSCs) based therapy is a promising approach to treat inflammatory disorders. However, therapeutic effect is not always achieved. Thus the mechanism involved in inflammation requires further elucidation. To explore the mechanisms by which MSCs respond to inflammatory stimuli, we investigated whether MSCs employed inflammasomes to participate in inflammation. Using in vitro and in vivo models, we found that canonical NLRP3 and non-canonical caspase-11 inflammasomes were activated in bone-associated MSCs (BA-MSCs) to promote the inflammatory response. The NLRP3 inflammasome was activated to mainly elicit IL-1β/18 release, whereas the caspase-11 inflammasome managed pyroptosis. Furthermore, we sought a small molecule component (66PR) to inhibit the activation of inflammasomes in BA-MSCs, which consequently improved their survival and therapeutic potential in inflammation bowel diseases. These current findings indicated that MSCs themselves could directly promote the inflammatory response by an inflammasome-dependent pathway. Our observations suggested that inhibition of the proinflammatory property may improve MSCs utilization in inflammatory disorders. Keywords: Mesenchymal stromal cells, Inflammasome, NLRP3, Caspase-11, Pyroptosishttp://www.sciencedirect.com/science/article/pii/S2352396418301877 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yaozhen Chen Xiangyang Qin Qunxing An Jing Yi Fan Feng Dandan Yin Ning An Zheng Liu Lihong Weng Shouwen Chen Xingbin Hu Wen Yin |
spellingShingle |
Yaozhen Chen Xiangyang Qin Qunxing An Jing Yi Fan Feng Dandan Yin Ning An Zheng Liu Lihong Weng Shouwen Chen Xingbin Hu Wen Yin Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes EBioMedicine |
author_facet |
Yaozhen Chen Xiangyang Qin Qunxing An Jing Yi Fan Feng Dandan Yin Ning An Zheng Liu Lihong Weng Shouwen Chen Xingbin Hu Wen Yin |
author_sort |
Yaozhen Chen |
title |
Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes |
title_short |
Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes |
title_full |
Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes |
title_fullStr |
Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes |
title_full_unstemmed |
Mesenchymal Stromal Cells Directly Promote Inflammation by Canonical NLRP3 and Non-canonical Caspase-11 Inflammasomes |
title_sort |
mesenchymal stromal cells directly promote inflammation by canonical nlrp3 and non-canonical caspase-11 inflammasomes |
publisher |
Elsevier |
series |
EBioMedicine |
issn |
2352-3964 |
publishDate |
2018-06-01 |
description |
Mesenchymal stromal cells (MSCs) based therapy is a promising approach to treat inflammatory disorders. However, therapeutic effect is not always achieved. Thus the mechanism involved in inflammation requires further elucidation. To explore the mechanisms by which MSCs respond to inflammatory stimuli, we investigated whether MSCs employed inflammasomes to participate in inflammation. Using in vitro and in vivo models, we found that canonical NLRP3 and non-canonical caspase-11 inflammasomes were activated in bone-associated MSCs (BA-MSCs) to promote the inflammatory response. The NLRP3 inflammasome was activated to mainly elicit IL-1β/18 release, whereas the caspase-11 inflammasome managed pyroptosis. Furthermore, we sought a small molecule component (66PR) to inhibit the activation of inflammasomes in BA-MSCs, which consequently improved their survival and therapeutic potential in inflammation bowel diseases. These current findings indicated that MSCs themselves could directly promote the inflammatory response by an inflammasome-dependent pathway. Our observations suggested that inhibition of the proinflammatory property may improve MSCs utilization in inflammatory disorders. Keywords: Mesenchymal stromal cells, Inflammasome, NLRP3, Caspase-11, Pyroptosis |
url |
http://www.sciencedirect.com/science/article/pii/S2352396418301877 |
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