Cargando…
Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis
This study aimed to investigate the protective effects of erythrocyte-mediated endoplasmic reticulum (ER) stress in macrophages in hemorrhagic shock. An hemorrhagic shock model was established in male BALB/c mice. Animals were randomly divided into three groups (n = 8): control group (A), erythrocyt...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784501/ https://www.ncbi.nlm.nih.gov/pubmed/33225714 http://dx.doi.org/10.1177/0963689720950218 |
_version_ | 1783632302998290432 |
---|---|
author | Kang, Yi-Qun Yuan, Xiao-Hong Li, Zhen-Zhou Wang, Huan Zhou, Xiao-Fang Wang, Xiao-Xiao Zhang, Zi-Wei Feng, Yu-Feng Guo, Jian-Rong |
author_facet | Kang, Yi-Qun Yuan, Xiao-Hong Li, Zhen-Zhou Wang, Huan Zhou, Xiao-Fang Wang, Xiao-Xiao Zhang, Zi-Wei Feng, Yu-Feng Guo, Jian-Rong |
author_sort | Kang, Yi-Qun |
collection | PubMed |
description | This study aimed to investigate the protective effects of erythrocyte-mediated endoplasmic reticulum (ER) stress in macrophages in hemorrhagic shock. An hemorrhagic shock model was established in male BALB/c mice. Animals were randomly divided into three groups (n = 8): control group (A), erythrocyte reinfusion group (B), and TLR9 inhibition group (C). Eight healthy BALB/c mice were also included as group N (n = 8). Mice in group A were not treated, while mice in groups B and C were transfused with red blood cells separated from the blood of mice in group N. Flow cytometry was used to detect the expression of erythrocyte surface protein TLR9 in each group. Immunofluorescence assay was used to analyze the distribution and relative expression of protein STING in macrophages. Flow cytometry was used to analyze the expression of STING, ATF6, and IRE1 in macrophages. Enzyme-linked immunosorbent assay was used to analyze the levels of inflammatory signal molecules, including IFN-α, IFN-β, IL-6, CCL4, CCL5, and IL-6. FITC-Annexin V was used to analyze the apoptosis of immune cells (macrophages) in mouse blood samples and to detect the concentration of calcium ions in erythrocyte cytoplasm. The results showed that the expression of erythrocyte surface protein TLR9; the distribution of STING-positive cells in macrophages; the expressions of STING, ATF6, and IRE1 in macrophages; the levels of inflammatory signal molecules; the apoptosis rate of macrophages; and the intracellular calcium concentration in erythrocytes in group B were higher than those in group A, followed by group C. These results suggest that TLR9 regulates ER stress in macrophages of mice with hemorrhagic shock through the TLR9-cGAS-STING-IFN signaling pathway. Increased expression of TLR9 enhanced macrophage activity, reduced apoptosis, enhanced inflammatory response and immune response, and restored electrolyte level, which might be a therapeutic option for the treatment of hemorrhagic shock. |
format | Online Article Text |
id | pubmed-7784501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77845012021-01-14 Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis Kang, Yi-Qun Yuan, Xiao-Hong Li, Zhen-Zhou Wang, Huan Zhou, Xiao-Fang Wang, Xiao-Xiao Zhang, Zi-Wei Feng, Yu-Feng Guo, Jian-Rong Cell Transplant Original Article This study aimed to investigate the protective effects of erythrocyte-mediated endoplasmic reticulum (ER) stress in macrophages in hemorrhagic shock. An hemorrhagic shock model was established in male BALB/c mice. Animals were randomly divided into three groups (n = 8): control group (A), erythrocyte reinfusion group (B), and TLR9 inhibition group (C). Eight healthy BALB/c mice were also included as group N (n = 8). Mice in group A were not treated, while mice in groups B and C were transfused with red blood cells separated from the blood of mice in group N. Flow cytometry was used to detect the expression of erythrocyte surface protein TLR9 in each group. Immunofluorescence assay was used to analyze the distribution and relative expression of protein STING in macrophages. Flow cytometry was used to analyze the expression of STING, ATF6, and IRE1 in macrophages. Enzyme-linked immunosorbent assay was used to analyze the levels of inflammatory signal molecules, including IFN-α, IFN-β, IL-6, CCL4, CCL5, and IL-6. FITC-Annexin V was used to analyze the apoptosis of immune cells (macrophages) in mouse blood samples and to detect the concentration of calcium ions in erythrocyte cytoplasm. The results showed that the expression of erythrocyte surface protein TLR9; the distribution of STING-positive cells in macrophages; the expressions of STING, ATF6, and IRE1 in macrophages; the levels of inflammatory signal molecules; the apoptosis rate of macrophages; and the intracellular calcium concentration in erythrocytes in group B were higher than those in group A, followed by group C. These results suggest that TLR9 regulates ER stress in macrophages of mice with hemorrhagic shock through the TLR9-cGAS-STING-IFN signaling pathway. Increased expression of TLR9 enhanced macrophage activity, reduced apoptosis, enhanced inflammatory response and immune response, and restored electrolyte level, which might be a therapeutic option for the treatment of hemorrhagic shock. SAGE Publications 2020-11-23 /pmc/articles/PMC7784501/ /pubmed/33225714 http://dx.doi.org/10.1177/0963689720950218 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Kang, Yi-Qun Yuan, Xiao-Hong Li, Zhen-Zhou Wang, Huan Zhou, Xiao-Fang Wang, Xiao-Xiao Zhang, Zi-Wei Feng, Yu-Feng Guo, Jian-Rong Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis |
title | Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis |
title_full | Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis |
title_fullStr | Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis |
title_full_unstemmed | Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis |
title_short | Antishock Characteristics of Erythrocyte-mediated Endoplasmic Reticulum Stress in Macrophages in Severe Hemorrhagic Shock Environment Based on TLR9-cGAS-STING-IFN Signal Axis |
title_sort | antishock characteristics of erythrocyte-mediated endoplasmic reticulum stress in macrophages in severe hemorrhagic shock environment based on tlr9-cgas-sting-ifn signal axis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784501/ https://www.ncbi.nlm.nih.gov/pubmed/33225714 http://dx.doi.org/10.1177/0963689720950218 |
work_keys_str_mv | AT kangyiqun antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT yuanxiaohong antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT lizhenzhou antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT wanghuan antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT zhouxiaofang antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT wangxiaoxiao antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT zhangziwei antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT fengyufeng antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis AT guojianrong antishockcharacteristicsoferythrocytemediatedendoplasmicreticulumstressinmacrophagesinseverehemorrhagicshockenvironmentbasedontlr9cgasstingifnsignalaxis |