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Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro

Our previous work shows that dioleoylphosphatidylglycerol (DOPG) accelerates corneal epithelial healing in vitro and in vivo by unknown mechanisms. Prior data demonstrate that DOPG inhibits toll-like receptor (TLR) activation and inflammation induced by microbial components (pathogen-associated mole...

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Autores principales: Fowler, Teresa E., Choudhary, Vivek, Melnyk, Samuel, Farsi, Mishma, Chang, Luke Y., Fortingo, Nyemkuna, Chen, Xunsheng, Watsky, Mitchell A., Bollag, Wendy B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10059050/
https://www.ncbi.nlm.nih.gov/pubmed/36982926
http://dx.doi.org/10.3390/ijms24065839
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author Fowler, Teresa E.
Choudhary, Vivek
Melnyk, Samuel
Farsi, Mishma
Chang, Luke Y.
Fortingo, Nyemkuna
Chen, Xunsheng
Watsky, Mitchell A.
Bollag, Wendy B.
author_facet Fowler, Teresa E.
Choudhary, Vivek
Melnyk, Samuel
Farsi, Mishma
Chang, Luke Y.
Fortingo, Nyemkuna
Chen, Xunsheng
Watsky, Mitchell A.
Bollag, Wendy B.
author_sort Fowler, Teresa E.
collection PubMed
description Our previous work shows that dioleoylphosphatidylglycerol (DOPG) accelerates corneal epithelial healing in vitro and in vivo by unknown mechanisms. Prior data demonstrate that DOPG inhibits toll-like receptor (TLR) activation and inflammation induced by microbial components (pathogen-associated molecular patterns, PAMPs) and by endogenous molecules upregulated in psoriatic skin, which act as danger-associated molecular patterns (DAMPs) to activate TLRs and promote inflammation. In the injured cornea, sterile inflammation can result from the release of the DAMP molecule, heat shock protein B4 (HSPB4), to contribute to delayed wound healing. Here, we show in vitro that DOPG inhibits TLR2 activation induced in response to HSPB4, as well as DAMPs that are elevated in diabetes, a disease that also slows corneal wound healing. Further, we show that the co-receptor, cluster of differentiation-14 (CD14), is necessary for PAMP/DAMP-induced activation of TLR2, as well as of TLR4. Finally, we simulated the high-glucose environment of diabetes to show that elevated glucose levels enhance TLR4 activation by a DAMP known to be upregulated in diabetes. Together, our results demonstrate the anti-inflammatory actions of DOPG and support further investigation into its development as a possible therapy for corneal injury, especially in diabetic patients at high risk of vision-threatening complications.
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spelling pubmed-100590502023-03-30 Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro Fowler, Teresa E. Choudhary, Vivek Melnyk, Samuel Farsi, Mishma Chang, Luke Y. Fortingo, Nyemkuna Chen, Xunsheng Watsky, Mitchell A. Bollag, Wendy B. Int J Mol Sci Article Our previous work shows that dioleoylphosphatidylglycerol (DOPG) accelerates corneal epithelial healing in vitro and in vivo by unknown mechanisms. Prior data demonstrate that DOPG inhibits toll-like receptor (TLR) activation and inflammation induced by microbial components (pathogen-associated molecular patterns, PAMPs) and by endogenous molecules upregulated in psoriatic skin, which act as danger-associated molecular patterns (DAMPs) to activate TLRs and promote inflammation. In the injured cornea, sterile inflammation can result from the release of the DAMP molecule, heat shock protein B4 (HSPB4), to contribute to delayed wound healing. Here, we show in vitro that DOPG inhibits TLR2 activation induced in response to HSPB4, as well as DAMPs that are elevated in diabetes, a disease that also slows corneal wound healing. Further, we show that the co-receptor, cluster of differentiation-14 (CD14), is necessary for PAMP/DAMP-induced activation of TLR2, as well as of TLR4. Finally, we simulated the high-glucose environment of diabetes to show that elevated glucose levels enhance TLR4 activation by a DAMP known to be upregulated in diabetes. Together, our results demonstrate the anti-inflammatory actions of DOPG and support further investigation into its development as a possible therapy for corneal injury, especially in diabetic patients at high risk of vision-threatening complications. MDPI 2023-03-19 /pmc/articles/PMC10059050/ /pubmed/36982926 http://dx.doi.org/10.3390/ijms24065839 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fowler, Teresa E.
Choudhary, Vivek
Melnyk, Samuel
Farsi, Mishma
Chang, Luke Y.
Fortingo, Nyemkuna
Chen, Xunsheng
Watsky, Mitchell A.
Bollag, Wendy B.
Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro
title Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro
title_full Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro
title_fullStr Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro
title_full_unstemmed Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro
title_short Dioleoylphosphatidylglycerol Inhibits Heat Shock Protein B4 (HSPB4)-Induced Inflammatory Pathways In Vitro
title_sort dioleoylphosphatidylglycerol inhibits heat shock protein b4 (hspb4)-induced inflammatory pathways in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10059050/
https://www.ncbi.nlm.nih.gov/pubmed/36982926
http://dx.doi.org/10.3390/ijms24065839
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