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103 Differences in Estradiol Levels Following Burn Injury

INTRODUCTION: The American Burn Association estimates over one million people with burn injuries in the US need medical care, with around 4,500 cases ending in mortality each year. Mortality is due to bacterial infection as a consequence of severe cytokine dysregulation and impaired wound healing. P...

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Autores principales: Willis, Micah L, Soliman, Daniel S, Ngeve, Sally-Irene, Mahung, Cressida, Wallet, Shannon, Maile, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946291/
http://dx.doi.org/10.1093/jbcr/irac012.106
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author Willis, Micah L
Soliman, Daniel S
Ngeve, Sally-Irene
Mahung, Cressida
Wallet, Shannon
Maile, Robert
author_facet Willis, Micah L
Soliman, Daniel S
Ngeve, Sally-Irene
Mahung, Cressida
Wallet, Shannon
Maile, Robert
author_sort Willis, Micah L
collection PubMed
description INTRODUCTION: The American Burn Association estimates over one million people with burn injuries in the US need medical care, with around 4,500 cases ending in mortality each year. Mortality is due to bacterial infection as a consequence of severe cytokine dysregulation and impaired wound healing. Previous research has shown females have worse outcomes than males following burn injury, but the reasoning is unknown. Estradiol is involved in the regulation of local and systemic interleukin-6 (IL-6) levels, which has been demonstrated by others to positively correlates with poor outcomes following burn. We hypothesize that concentrations of Estrogen can create a pro-inflammatory effect in epithelial cells, which is controlled in a negative feedback loop. METHODS: We utilized plasma from 1) human burn patients and 2) our murine model of burn injury, in which C57BL/6 mice are exposed to a 20% total body surface area burn injury and 3) an in vitro cell model using human Oral Epithelial Cells (OECs) and human Airway Epithelial Cells (AECs). RESULTS: We measured human estradiol levels 1-3 days after burn injury and murine estradiol levels 3 and 7 days after injury by ELISA. In humans there were differences in levels at these timepoints (p< 0.05). In mice we observed a difference in the change in murine estradiol levels between males and females 7 days after injury (p < 0.01). We simulated a wound by removing the cell insert and treating cells with concentrations of estradiol (0.1 nM, 1.0 nM & 250 nM). Images were taken at 0, 6 & 24 H and analyzed using Fiji to observe wound closure. Supernatant was removed from cells at 24 H and analyzed for IL-6 levels (a key pro-inflammatory cytokine linked to poor wound healing after burn) via ELISA. mRNA was isolated from cells and analyzed for IL-6, TNFα & VEGF (important regulators of wound healing) via PCR. We observed an increase in percent wound closure in the AECs, and no difference in OECs. We observed an increase in IL-6 production following stimulation with Estradiol and LPS at different rates for each cell type and corresponding reduction in TNFα and VEGF expression. We also described different Estradiol Receptors in the two cell types. CONCLUSIONS: Taken together, these data suggest burn injury upregulates estradiol in both humans and mice following burn injury whereby this is more robust in females at later stages of burn injury and thus contributing to female-associated poor clinical outcomes.
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spelling pubmed-89462912022-03-28 103 Differences in Estradiol Levels Following Burn Injury Willis, Micah L Soliman, Daniel S Ngeve, Sally-Irene Mahung, Cressida Wallet, Shannon Maile, Robert J Burn Care Res Correlative XIII: Translational Sciences: Critical Care and Metabolism INTRODUCTION: The American Burn Association estimates over one million people with burn injuries in the US need medical care, with around 4,500 cases ending in mortality each year. Mortality is due to bacterial infection as a consequence of severe cytokine dysregulation and impaired wound healing. Previous research has shown females have worse outcomes than males following burn injury, but the reasoning is unknown. Estradiol is involved in the regulation of local and systemic interleukin-6 (IL-6) levels, which has been demonstrated by others to positively correlates with poor outcomes following burn. We hypothesize that concentrations of Estrogen can create a pro-inflammatory effect in epithelial cells, which is controlled in a negative feedback loop. METHODS: We utilized plasma from 1) human burn patients and 2) our murine model of burn injury, in which C57BL/6 mice are exposed to a 20% total body surface area burn injury and 3) an in vitro cell model using human Oral Epithelial Cells (OECs) and human Airway Epithelial Cells (AECs). RESULTS: We measured human estradiol levels 1-3 days after burn injury and murine estradiol levels 3 and 7 days after injury by ELISA. In humans there were differences in levels at these timepoints (p< 0.05). In mice we observed a difference in the change in murine estradiol levels between males and females 7 days after injury (p < 0.01). We simulated a wound by removing the cell insert and treating cells with concentrations of estradiol (0.1 nM, 1.0 nM & 250 nM). Images were taken at 0, 6 & 24 H and analyzed using Fiji to observe wound closure. Supernatant was removed from cells at 24 H and analyzed for IL-6 levels (a key pro-inflammatory cytokine linked to poor wound healing after burn) via ELISA. mRNA was isolated from cells and analyzed for IL-6, TNFα & VEGF (important regulators of wound healing) via PCR. We observed an increase in percent wound closure in the AECs, and no difference in OECs. We observed an increase in IL-6 production following stimulation with Estradiol and LPS at different rates for each cell type and corresponding reduction in TNFα and VEGF expression. We also described different Estradiol Receptors in the two cell types. CONCLUSIONS: Taken together, these data suggest burn injury upregulates estradiol in both humans and mice following burn injury whereby this is more robust in females at later stages of burn injury and thus contributing to female-associated poor clinical outcomes. Oxford University Press 2022-03-23 /pmc/articles/PMC8946291/ http://dx.doi.org/10.1093/jbcr/irac012.106 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the American Burn Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Correlative XIII: Translational Sciences: Critical Care and Metabolism
Willis, Micah L
Soliman, Daniel S
Ngeve, Sally-Irene
Mahung, Cressida
Wallet, Shannon
Maile, Robert
103 Differences in Estradiol Levels Following Burn Injury
title 103 Differences in Estradiol Levels Following Burn Injury
title_full 103 Differences in Estradiol Levels Following Burn Injury
title_fullStr 103 Differences in Estradiol Levels Following Burn Injury
title_full_unstemmed 103 Differences in Estradiol Levels Following Burn Injury
title_short 103 Differences in Estradiol Levels Following Burn Injury
title_sort 103 differences in estradiol levels following burn injury
topic Correlative XIII: Translational Sciences: Critical Care and Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946291/
http://dx.doi.org/10.1093/jbcr/irac012.106
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