Cargando…
Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation
Type 1 diabetes (T1D) imposes a significant health burden by negatively affecting tissue regeneration during wound healing. The adverse effect of diabetes is attributed to high levels of inflammation, but the cellular mechanisms responsible remain elusive. In this study, we show that intrinsic skele...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804629/ https://www.ncbi.nlm.nih.gov/pubmed/31439641 http://dx.doi.org/10.2337/db19-0496 |
_version_ | 1783461238887415808 |
---|---|
author | Ko, Kang I. Syverson, Abby L. Kralik, Richard M. Choi, Jerry DerGarabedian, Brett P. Chen, Chider Graves, Dana T. |
author_facet | Ko, Kang I. Syverson, Abby L. Kralik, Richard M. Choi, Jerry DerGarabedian, Brett P. Chen, Chider Graves, Dana T. |
author_sort | Ko, Kang I. |
collection | PubMed |
description | Type 1 diabetes (T1D) imposes a significant health burden by negatively affecting tissue regeneration during wound healing. The adverse effect of diabetes is attributed to high levels of inflammation, but the cellular mechanisms responsible remain elusive. In this study, we show that intrinsic skeletal stem cells (SSCs), a subset of mesenchymal stem cells, are essential for resolution of inflammation to occur during osseous healing by using genetic approaches to selectively ablate SSCs. T1D caused aberrant nuclear factor-κB (NF-κB) activation in SSCs and substantially enhanced inflammation in vivo. Constitutive or tamoxifen-induced inhibition of NF-κB in SSCs rescued the impact of diabetes on inflammation, SSC expansion, and tissue formation. In contrast, NF-κB inhibition in chondrocytes failed to reverse the effect of T1D. Mechanistically, diabetes caused defective proresolving macrophage (M2) polarization by reducing TGF-β1 expression by SSCs, which was recovered by NF-κB inhibition or exogenous TGF-β1 treatment. These data identify an underlying mechanism for altered healing in T1D and demonstrate that diabetes induces NF-κB hyperactivation in SSCs to disrupt their ability to modulate M2 polarization and resolve inflammation. |
format | Online Article Text |
id | pubmed-6804629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-68046292020-11-01 Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation Ko, Kang I. Syverson, Abby L. Kralik, Richard M. Choi, Jerry DerGarabedian, Brett P. Chen, Chider Graves, Dana T. Diabetes Complications Type 1 diabetes (T1D) imposes a significant health burden by negatively affecting tissue regeneration during wound healing. The adverse effect of diabetes is attributed to high levels of inflammation, but the cellular mechanisms responsible remain elusive. In this study, we show that intrinsic skeletal stem cells (SSCs), a subset of mesenchymal stem cells, are essential for resolution of inflammation to occur during osseous healing by using genetic approaches to selectively ablate SSCs. T1D caused aberrant nuclear factor-κB (NF-κB) activation in SSCs and substantially enhanced inflammation in vivo. Constitutive or tamoxifen-induced inhibition of NF-κB in SSCs rescued the impact of diabetes on inflammation, SSC expansion, and tissue formation. In contrast, NF-κB inhibition in chondrocytes failed to reverse the effect of T1D. Mechanistically, diabetes caused defective proresolving macrophage (M2) polarization by reducing TGF-β1 expression by SSCs, which was recovered by NF-κB inhibition or exogenous TGF-β1 treatment. These data identify an underlying mechanism for altered healing in T1D and demonstrate that diabetes induces NF-κB hyperactivation in SSCs to disrupt their ability to modulate M2 polarization and resolve inflammation. American Diabetes Association 2019-11 2019-08-22 /pmc/articles/PMC6804629/ /pubmed/31439641 http://dx.doi.org/10.2337/db19-0496 Text en © 2019 by the American Diabetes Association. http://www.diabetesjournals.org/content/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license. |
spellingShingle | Complications Ko, Kang I. Syverson, Abby L. Kralik, Richard M. Choi, Jerry DerGarabedian, Brett P. Chen, Chider Graves, Dana T. Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation |
title | Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation |
title_full | Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation |
title_fullStr | Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation |
title_full_unstemmed | Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation |
title_short | Diabetes-Induced NF-κB Dysregulation in Skeletal Stem Cells Prevents Resolution of Inflammation |
title_sort | diabetes-induced nf-κb dysregulation in skeletal stem cells prevents resolution of inflammation |
topic | Complications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804629/ https://www.ncbi.nlm.nih.gov/pubmed/31439641 http://dx.doi.org/10.2337/db19-0496 |
work_keys_str_mv | AT kokangi diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation AT syversonabbyl diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation AT kralikrichardm diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation AT choijerry diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation AT dergarabedianbrettp diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation AT chenchider diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation AT gravesdanat diabetesinducednfkbdysregulationinskeletalstemcellspreventsresolutionofinflammation |