Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia

Vascular intimal hyperplasia (VIH) is an important stage of atherosclerosis (AS), in which macrophages not only play a critical role in local inflammation, but also transform into foam cells to participate into plaque formation, where they appear to be heterogeneous. Recently, it was shown that CD11...

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Main Authors: Jiaquan Chen, Weilun Wang, Qihong Ni, Lan Zhang, Xiangjiang Guo
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.952164/full
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author Jiaquan Chen
Weilun Wang
Qihong Ni
Lan Zhang
Xiangjiang Guo
author_facet Jiaquan Chen
Weilun Wang
Qihong Ni
Lan Zhang
Xiangjiang Guo
author_sort Jiaquan Chen
collection DOAJ
description Vascular intimal hyperplasia (VIH) is an important stage of atherosclerosis (AS), in which macrophages not only play a critical role in local inflammation, but also transform into foam cells to participate into plaque formation, where they appear to be heterogeneous. Recently, it was shown that CD11c+ macrophages were more associated with active plaque progression. However, the molecular regulation of phenotypic changes of plaque macrophages during VIH has not been clarified and thus addressed in the current study. Since CD11c- cells were M2a-polarized anti-inflammatory macrophages, while CD11c+ cells were M1/M2b-polarized pro-inflammatory macrophages, we used bioinformatics tools to analyze the CD11c+ versus CD11c- plaque macrophages, aiming to detect the differential genes associated with M1/M2 macrophage polarization. We obtained 122 differential genes that were significantly altered in CD11c+ versus CD11c- plaque macrophages, regardless of CD11b expression. Next, hub genes were predicted in these 122 genes, from which we detected 3 candidates, interleukin 6 (Il6), Decorin (Dcn) and Tissue inhibitor matrix metalloproteinase 1 (Timp1). The effects of these 3 genes on CD11c expression as well as on the macrophage polarization were assessed in vitro, showing that only expression of Il6, but not expression of Dcn or Timp1, induced M1/M2b-like polarization in M2a macrophages. Moreover, only suppression of Il6, but not suppression of either of Dcn or Timp1, induced M2a-like polarization in M1/M2b macrophages. Furthermore, pharmaceutical suppression of Il6 attenuated VIH formation and progression of AS in a mouse model that co-applied apolipoprotein E-knockout and high-fat diet. Together, our data suggest that formation of VIH can be controlled through modulating macrophage polarization, as a promising therapeutic approach for prevent AS.
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spelling doaj.art-9d5d403d7da646b481193ffd389623d42022-12-22T02:07:39ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-07-011310.3389/fimmu.2022.952164952164Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasiaJiaquan ChenWeilun WangQihong NiLan ZhangXiangjiang GuoVascular intimal hyperplasia (VIH) is an important stage of atherosclerosis (AS), in which macrophages not only play a critical role in local inflammation, but also transform into foam cells to participate into plaque formation, where they appear to be heterogeneous. Recently, it was shown that CD11c+ macrophages were more associated with active plaque progression. However, the molecular regulation of phenotypic changes of plaque macrophages during VIH has not been clarified and thus addressed in the current study. Since CD11c- cells were M2a-polarized anti-inflammatory macrophages, while CD11c+ cells were M1/M2b-polarized pro-inflammatory macrophages, we used bioinformatics tools to analyze the CD11c+ versus CD11c- plaque macrophages, aiming to detect the differential genes associated with M1/M2 macrophage polarization. We obtained 122 differential genes that were significantly altered in CD11c+ versus CD11c- plaque macrophages, regardless of CD11b expression. Next, hub genes were predicted in these 122 genes, from which we detected 3 candidates, interleukin 6 (Il6), Decorin (Dcn) and Tissue inhibitor matrix metalloproteinase 1 (Timp1). The effects of these 3 genes on CD11c expression as well as on the macrophage polarization were assessed in vitro, showing that only expression of Il6, but not expression of Dcn or Timp1, induced M1/M2b-like polarization in M2a macrophages. Moreover, only suppression of Il6, but not suppression of either of Dcn or Timp1, induced M2a-like polarization in M1/M2b macrophages. Furthermore, pharmaceutical suppression of Il6 attenuated VIH formation and progression of AS in a mouse model that co-applied apolipoprotein E-knockout and high-fat diet. Together, our data suggest that formation of VIH can be controlled through modulating macrophage polarization, as a promising therapeutic approach for prevent AS.https://www.frontiersin.org/articles/10.3389/fimmu.2022.952164/fullatherosclerosisvascular intimal hyperplasiamacrophage polarizationinterleukin 6plaques
spellingShingle Jiaquan Chen
Weilun Wang
Qihong Ni
Lan Zhang
Xiangjiang Guo
Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia
Frontiers in Immunology
atherosclerosis
vascular intimal hyperplasia
macrophage polarization
interleukin 6
plaques
title Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia
title_full Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia
title_fullStr Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia
title_full_unstemmed Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia
title_short Interleukin 6-regulated macrophage polarization controls atherosclerosis-associated vascular intimal hyperplasia
title_sort interleukin 6 regulated macrophage polarization controls atherosclerosis associated vascular intimal hyperplasia
topic atherosclerosis
vascular intimal hyperplasia
macrophage polarization
interleukin 6
plaques
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.952164/full
work_keys_str_mv AT jiaquanchen interleukin6regulatedmacrophagepolarizationcontrolsatherosclerosisassociatedvascularintimalhyperplasia
AT weilunwang interleukin6regulatedmacrophagepolarizationcontrolsatherosclerosisassociatedvascularintimalhyperplasia
AT qihongni interleukin6regulatedmacrophagepolarizationcontrolsatherosclerosisassociatedvascularintimalhyperplasia
AT lanzhang interleukin6regulatedmacrophagepolarizationcontrolsatherosclerosisassociatedvascularintimalhyperplasia
AT xiangjiangguo interleukin6regulatedmacrophagepolarizationcontrolsatherosclerosisassociatedvascularintimalhyperplasia