Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia‒reperfusion
Rationale: The transition from acute inflammation to fibrosis following myocardial ischemia‒reperfusion (MIR) significantly affects prognosis. Macrophages play a pivotal role in inflammatory damage and repair after MIR. However, the heterogeneity and transformation mechanisms of macrophages during t...
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Veröffentlicht in: | Theranostics 2024-01, Vol.14 (3), p.1241-1259 |
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creator | Shen, Shichun Zhang, Meng Wang, Xiaohe Liu, Qiaoling Su, Huimin Sun, Bingyi Guo, Zhiqing Tian, Beiduo Gan, Hong Gong, Chen Ma, Likun |
description | Rationale: The transition from acute inflammation to fibrosis following myocardial ischemia‒reperfusion (MIR) significantly affects prognosis. Macrophages play a pivotal role in inflammatory damage and repair after MIR. However, the heterogeneity and transformation mechanisms of macrophages during this transition are not well understood. Methods: In this study, we used single-cell RNA sequencing (scRNA-seq) and mass cytometry to examine murine monocyte-derived macrophages after MIR to investigate macrophage subtypes and their roles in the MIR process. S100a9-/- mice were used to establish MIR model to clarify the mechanism of alleviating inflammation and fibrosis after MIR. Reinfusion of bone marrow-derived macrophages (BMDMs) after macrophage depletion (MD) in mice subjected to MIR were performed to further examine the role of S100a9hi macrophages in MIR. Results: We identified a unique subtype of S100a9hi macrophages that originate from monocytes and are involved in acute inflammation and fibrosis. These S100a9hi macrophages infiltrate the heart as early as 2 h post-reperfusion and activate the Myd88/NFκB/NLRP3 signaling pathway, amplifying inflammatory responses. As the tissue environment shifts from proinflammatory to reparative, S100a9 activates transforming growth factor-β (Tgf-β)/p-smad3 signaling. This activation not only induces the transformation of myocardial fibroblasts to myofibroblasts but also promotes fibrosis via the macrophage-to-myofibroblast transition (MMT). Targeting S100a9 with a specific inhibitor could effectively mitigate acute inflammatory damage and halt the progression of fibrosis, including MMT. Conclusion: S100a9hi macrophages are a promising therapeutic target for managing the transition from inflammation to fibrosis after MIR. |
doi_str_mv | 10.7150/thno.91180 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10845204</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2923329516</sourcerecordid><originalsourceid>FETCH-LOGICAL-p280t-adbd4580e7236a34c56e2165a0253c7500de65ebfa4af98bb6431ac7b1807a163</originalsourceid><addsrcrecordid>eNpVUMtKxTAQLYLg5erGL8jSTa9J2vSxEhFfIAo-1mWaTm8jTVKT9MLd-Q3-gz_mlxj1bhwYBs4w58w5SXLM6Kpkgp6GwdhVzVhF95IFq7IqLYucHiRH3r_SWDnlNasXyeeTMusRU4njSB7vz4nHtxmNjChxuEEYPXlilEI9KKJBOjsNsEZPJme1DUjCENuB8Sooa0gfYQJyjhtl-hG0hl88WNKr1tmgZOTVtsPxRwL6gI7orZXgOgUjUV4OqBV8vX84nND1s4_nh8l-Hz_Bo91cJi9Xl88XN-ndw_XtxfldOvGKhhS6tstFRbHkWQFZLkWBnBUCKBeZLAWlHRYC2x5y6OuqbYs8YyDLNsZUAiuyZXL2xzvNrcZOoonWxmZySoPbNhZU839j1NCs7aZhtMoFp3lkONkxOBuD9KHR0VIMFwza2Te85lnGaxHFvgEwAIpH</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2923329516</pqid></control><display><type>article</type><title>Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia‒reperfusion</title><source>PubMed Central Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Shen, Shichun ; Zhang, Meng ; Wang, Xiaohe ; Liu, Qiaoling ; Su, Huimin ; Sun, Bingyi ; Guo, Zhiqing ; Tian, Beiduo ; Gan, Hong ; Gong, Chen ; Ma, Likun</creator><creatorcontrib>Shen, Shichun ; Zhang, Meng ; Wang, Xiaohe ; Liu, Qiaoling ; Su, Huimin ; Sun, Bingyi ; Guo, Zhiqing ; Tian, Beiduo ; Gan, Hong ; Gong, Chen ; Ma, Likun</creatorcontrib><description>Rationale: The transition from acute inflammation to fibrosis following myocardial ischemia‒reperfusion (MIR) significantly affects prognosis. Macrophages play a pivotal role in inflammatory damage and repair after MIR. However, the heterogeneity and transformation mechanisms of macrophages during this transition are not well understood. Methods: In this study, we used single-cell RNA sequencing (scRNA-seq) and mass cytometry to examine murine monocyte-derived macrophages after MIR to investigate macrophage subtypes and their roles in the MIR process. S100a9-/- mice were used to establish MIR model to clarify the mechanism of alleviating inflammation and fibrosis after MIR. Reinfusion of bone marrow-derived macrophages (BMDMs) after macrophage depletion (MD) in mice subjected to MIR were performed to further examine the role of S100a9hi macrophages in MIR. Results: We identified a unique subtype of S100a9hi macrophages that originate from monocytes and are involved in acute inflammation and fibrosis. These S100a9hi macrophages infiltrate the heart as early as 2 h post-reperfusion and activate the Myd88/NFκB/NLRP3 signaling pathway, amplifying inflammatory responses. As the tissue environment shifts from proinflammatory to reparative, S100a9 activates transforming growth factor-β (Tgf-β)/p-smad3 signaling. This activation not only induces the transformation of myocardial fibroblasts to myofibroblasts but also promotes fibrosis via the macrophage-to-myofibroblast transition (MMT). Targeting S100a9 with a specific inhibitor could effectively mitigate acute inflammatory damage and halt the progression of fibrosis, including MMT. Conclusion: S100a9hi macrophages are a promising therapeutic target for managing the transition from inflammation to fibrosis after MIR.</description><identifier>EISSN: 1838-7640</identifier><identifier>DOI: 10.7150/thno.91180</identifier><language>eng</language><publisher>Sydney: Ivyspring International Publisher</publisher><subject>Research Paper</subject><ispartof>Theranostics, 2024-01, Vol.14 (3), p.1241-1259</ispartof><rights>The author(s) 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10845204/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10845204/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27928,27929,53795,53797</link.rule.ids></links><search><creatorcontrib>Shen, Shichun</creatorcontrib><creatorcontrib>Zhang, Meng</creatorcontrib><creatorcontrib>Wang, Xiaohe</creatorcontrib><creatorcontrib>Liu, Qiaoling</creatorcontrib><creatorcontrib>Su, Huimin</creatorcontrib><creatorcontrib>Sun, Bingyi</creatorcontrib><creatorcontrib>Guo, Zhiqing</creatorcontrib><creatorcontrib>Tian, Beiduo</creatorcontrib><creatorcontrib>Gan, Hong</creatorcontrib><creatorcontrib>Gong, Chen</creatorcontrib><creatorcontrib>Ma, Likun</creatorcontrib><title>Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia‒reperfusion</title><title>Theranostics</title><description>Rationale: The transition from acute inflammation to fibrosis following myocardial ischemia‒reperfusion (MIR) significantly affects prognosis. Macrophages play a pivotal role in inflammatory damage and repair after MIR. However, the heterogeneity and transformation mechanisms of macrophages during this transition are not well understood. Methods: In this study, we used single-cell RNA sequencing (scRNA-seq) and mass cytometry to examine murine monocyte-derived macrophages after MIR to investigate macrophage subtypes and their roles in the MIR process. S100a9-/- mice were used to establish MIR model to clarify the mechanism of alleviating inflammation and fibrosis after MIR. Reinfusion of bone marrow-derived macrophages (BMDMs) after macrophage depletion (MD) in mice subjected to MIR were performed to further examine the role of S100a9hi macrophages in MIR. Results: We identified a unique subtype of S100a9hi macrophages that originate from monocytes and are involved in acute inflammation and fibrosis. These S100a9hi macrophages infiltrate the heart as early as 2 h post-reperfusion and activate the Myd88/NFκB/NLRP3 signaling pathway, amplifying inflammatory responses. As the tissue environment shifts from proinflammatory to reparative, S100a9 activates transforming growth factor-β (Tgf-β)/p-smad3 signaling. This activation not only induces the transformation of myocardial fibroblasts to myofibroblasts but also promotes fibrosis via the macrophage-to-myofibroblast transition (MMT). Targeting S100a9 with a specific inhibitor could effectively mitigate acute inflammatory damage and halt the progression of fibrosis, including MMT. Conclusion: S100a9hi macrophages are a promising therapeutic target for managing the transition from inflammation to fibrosis after MIR.</description><subject>Research Paper</subject><issn>1838-7640</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVUMtKxTAQLYLg5erGL8jSTa9J2vSxEhFfIAo-1mWaTm8jTVKT9MLd-Q3-gz_mlxj1bhwYBs4w58w5SXLM6Kpkgp6GwdhVzVhF95IFq7IqLYucHiRH3r_SWDnlNasXyeeTMusRU4njSB7vz4nHtxmNjChxuEEYPXlilEI9KKJBOjsNsEZPJme1DUjCENuB8Sooa0gfYQJyjhtl-hG0hl88WNKr1tmgZOTVtsPxRwL6gI7orZXgOgUjUV4OqBV8vX84nND1s4_nh8l-Hz_Bo91cJi9Xl88XN-ndw_XtxfldOvGKhhS6tstFRbHkWQFZLkWBnBUCKBeZLAWlHRYC2x5y6OuqbYs8YyDLNsZUAiuyZXL2xzvNrcZOoonWxmZySoPbNhZU839j1NCs7aZhtMoFp3lkONkxOBuD9KHR0VIMFwza2Te85lnGaxHFvgEwAIpH</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Shen, Shichun</creator><creator>Zhang, Meng</creator><creator>Wang, Xiaohe</creator><creator>Liu, Qiaoling</creator><creator>Su, Huimin</creator><creator>Sun, Bingyi</creator><creator>Guo, Zhiqing</creator><creator>Tian, Beiduo</creator><creator>Gan, Hong</creator><creator>Gong, Chen</creator><creator>Ma, Likun</creator><general>Ivyspring International Publisher</general><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240101</creationdate><title>Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia‒reperfusion</title><author>Shen, Shichun ; Zhang, Meng ; Wang, Xiaohe ; Liu, Qiaoling ; Su, Huimin ; Sun, Bingyi ; Guo, Zhiqing ; Tian, Beiduo ; Gan, Hong ; Gong, Chen ; Ma, Likun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p280t-adbd4580e7236a34c56e2165a0253c7500de65ebfa4af98bb6431ac7b1807a163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Research Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Shichun</creatorcontrib><creatorcontrib>Zhang, Meng</creatorcontrib><creatorcontrib>Wang, Xiaohe</creatorcontrib><creatorcontrib>Liu, Qiaoling</creatorcontrib><creatorcontrib>Su, Huimin</creatorcontrib><creatorcontrib>Sun, Bingyi</creatorcontrib><creatorcontrib>Guo, Zhiqing</creatorcontrib><creatorcontrib>Tian, Beiduo</creatorcontrib><creatorcontrib>Gan, Hong</creatorcontrib><creatorcontrib>Gong, Chen</creatorcontrib><creatorcontrib>Ma, Likun</creatorcontrib><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Theranostics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Shichun</au><au>Zhang, Meng</au><au>Wang, Xiaohe</au><au>Liu, Qiaoling</au><au>Su, Huimin</au><au>Sun, Bingyi</au><au>Guo, Zhiqing</au><au>Tian, Beiduo</au><au>Gan, Hong</au><au>Gong, Chen</au><au>Ma, Likun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia‒reperfusion</atitle><jtitle>Theranostics</jtitle><date>2024-01-01</date><risdate>2024</risdate><volume>14</volume><issue>3</issue><spage>1241</spage><epage>1259</epage><pages>1241-1259</pages><eissn>1838-7640</eissn><abstract>Rationale: The transition from acute inflammation to fibrosis following myocardial ischemia‒reperfusion (MIR) significantly affects prognosis. Macrophages play a pivotal role in inflammatory damage and repair after MIR. However, the heterogeneity and transformation mechanisms of macrophages during this transition are not well understood. Methods: In this study, we used single-cell RNA sequencing (scRNA-seq) and mass cytometry to examine murine monocyte-derived macrophages after MIR to investigate macrophage subtypes and their roles in the MIR process. S100a9-/- mice were used to establish MIR model to clarify the mechanism of alleviating inflammation and fibrosis after MIR. Reinfusion of bone marrow-derived macrophages (BMDMs) after macrophage depletion (MD) in mice subjected to MIR were performed to further examine the role of S100a9hi macrophages in MIR. Results: We identified a unique subtype of S100a9hi macrophages that originate from monocytes and are involved in acute inflammation and fibrosis. These S100a9hi macrophages infiltrate the heart as early as 2 h post-reperfusion and activate the Myd88/NFκB/NLRP3 signaling pathway, amplifying inflammatory responses. As the tissue environment shifts from proinflammatory to reparative, S100a9 activates transforming growth factor-β (Tgf-β)/p-smad3 signaling. This activation not only induces the transformation of myocardial fibroblasts to myofibroblasts but also promotes fibrosis via the macrophage-to-myofibroblast transition (MMT). Targeting S100a9 with a specific inhibitor could effectively mitigate acute inflammatory damage and halt the progression of fibrosis, including MMT. Conclusion: S100a9hi macrophages are a promising therapeutic target for managing the transition from inflammation to fibrosis after MIR.</abstract><cop>Sydney</cop><pub>Ivyspring International Publisher</pub><doi>10.7150/thno.91180</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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title | Single-cell RNA sequencing reveals S100a9hi macrophages promote the transition from acute inflammation to fibrotic remodeling after myocardial ischemia‒reperfusion |
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