Hematopoietic stem and multipotent progenitor cells produce IL-17, IL-21 and other cytokines in response to TLR signals associated with late apoptotic products and augment memory Th17 and Tc17 cells in the bone marrow of normal and lupus mice

Copyright © 2015 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 162(2016) vom: 15. Jan., Seite 9-26
1. Verfasser: Chen, Ching-I (VerfasserIn)
Weitere Verfasser: Zhang, Li, Datta, Syamal K
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2016
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, N.I.H., Extramural Apoptosis Bone marrow Cytokines Hematopoietic progenitors Lupus Memory Th17/Tc17 cells TLR signals CD4 Antigens mehr... CD8 Antigens IL17A protein, human Interleukin-17 Interleukins Toll-Like Receptors Interleukin-21 MKM3CA6LT1
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245 1 0 |a Hematopoietic stem and multipotent progenitor cells produce IL-17, IL-21 and other cytokines in response to TLR signals associated with late apoptotic products and augment memory Th17 and Tc17 cells in the bone marrow of normal and lupus mice 
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500 |a Date Revised 03.01.2025 
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520 |a Copyright © 2015 Elsevier Inc. All rights reserved. 
520 |a We studied effects of early and late apoptotic (necroptotic) cell products, related damage associated alarmins and TLR agonists, on hematopoietic stem and progenitor cells (HSPC). Surprisingly, normal HSPC themselves produced IL-17 and IL-21 after 1½days of stimulation, and the best stimulators were TLR 7/8 agonist; HMGB1-DNA; TLR 9 agonist, and necroptotic B cells. The stimulated HSPC expressed additional cytokines/mediators, directly causing rapid expansion of IL-17(+) memory CD4 T (Th17), and CD8 T (Tc17) cells, and antigen-experienced IL-17(+) T cells with "naïve" phenotype. In lupus marrow, HSPC were spontaneously pre-stimulated by endogenous signals to produce IL-17 and IL-21. In contrast to HSPC, megakaryocyte progenitors (MKP) did not produce IL-17, and unlike HSPC, they could process and present particulate apoptotic autoantigens to augment autoimmune memory Th17 response. Thus abnormally stimulated primitive hematopoietic progenitors augment expansion of IL-17 producing immune and autoimmune memory T cells in the bone marrow, which may affect central tolerance 
650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Apoptosis 
650 4 |a Bone marrow 
650 4 |a Cytokines 
650 4 |a Hematopoietic progenitors 
650 4 |a Lupus 
650 4 |a Memory Th17/Tc17 cells 
650 4 |a TLR signals 
650 7 |a CD4 Antigens  |2 NLM 
650 7 |a CD8 Antigens  |2 NLM 
650 7 |a Cytokines  |2 NLM 
650 7 |a IL17A protein, human  |2 NLM 
650 7 |a Interleukin-17  |2 NLM 
650 7 |a Interleukins  |2 NLM 
650 7 |a Toll-Like Receptors  |2 NLM 
650 7 |a Interleukin-21  |2 NLM 
650 7 |a MKM3CA6LT1  |2 NLM 
700 1 |a Zhang, Li  |e verfasserin  |4 aut 
700 1 |a Datta, Syamal K  |e verfasserin  |4 aut 
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773 1 8 |g volume:162  |g year:2016  |g day:15  |g month:01  |g pages:9-26 
856 4 0 |u http://dx.doi.org/10.1016/j.clim.2015.10.007  |3 Volltext 
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