Megan E Amason, Cole J Beatty, Carissa K Harvest, Daniel R Saban, Edward A Miao
{"title":"先天性肉芽肿的趋化因子表达谱。","authors":"Megan E Amason, Cole J Beatty, Carissa K Harvest, Daniel R Saban, Edward A Miao","doi":"10.7554/eLife.96425","DOIUrl":null,"url":null,"abstract":"<p><p>Granulomas are defined by the presence of organized layers of immune cells that include macrophages. Granulomas are often characterized as a way for the immune system to contain an infection and prevent its dissemination. We recently established a mouse infection model where <i>Chromobacterium violaceum</i> induces the innate immune system to form granulomas in the liver. This response successfully eradicates the bacteria and returns the liver to homeostasis. Here, we sought to characterize the chemokines involved in directing immune cells to form the distinct layers of a granuloma. We use spatial transcriptomics to investigate the spatial and temporal expression of all CC and CXC chemokines and their receptors within this granuloma response. The expression profiles change dynamically over space and time as the granuloma matures and then resolves. To investigate the importance of monocyte-derived macrophages in this immune response, we studied the role of CCR2 during <i>C. violaceum</i> infection. <i>Ccr2</i><sup>-/-</sup> mice had negligible numbers of macrophages, but large numbers of neutrophils, in the <i>C. violaceum</i>-infected lesions. In addition, lesions had abnormal architecture resulting in loss of bacterial containment. Without CCR2, bacteria disseminated and the mice succumbed to the infection. This indicates that macrophages are critical to form a successful innate granuloma in response to <i>C. violaceum</i>.</p>","PeriodicalId":11640,"journal":{"name":"eLife","volume":"13 ","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11563579/pdf/","citationCount":"0","resultStr":"{\"title\":\"Chemokine expression profile of an innate granuloma.\",\"authors\":\"Megan E Amason, Cole J Beatty, Carissa K Harvest, Daniel R Saban, Edward A Miao\",\"doi\":\"10.7554/eLife.96425\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Granulomas are defined by the presence of organized layers of immune cells that include macrophages. Granulomas are often characterized as a way for the immune system to contain an infection and prevent its dissemination. We recently established a mouse infection model where <i>Chromobacterium violaceum</i> induces the innate immune system to form granulomas in the liver. This response successfully eradicates the bacteria and returns the liver to homeostasis. Here, we sought to characterize the chemokines involved in directing immune cells to form the distinct layers of a granuloma. We use spatial transcriptomics to investigate the spatial and temporal expression of all CC and CXC chemokines and their receptors within this granuloma response. The expression profiles change dynamically over space and time as the granuloma matures and then resolves. To investigate the importance of monocyte-derived macrophages in this immune response, we studied the role of CCR2 during <i>C. violaceum</i> infection. <i>Ccr2</i><sup>-/-</sup> mice had negligible numbers of macrophages, but large numbers of neutrophils, in the <i>C. violaceum</i>-infected lesions. In addition, lesions had abnormal architecture resulting in loss of bacterial containment. Without CCR2, bacteria disseminated and the mice succumbed to the infection. This indicates that macrophages are critical to form a successful innate granuloma in response to <i>C. violaceum</i>.</p>\",\"PeriodicalId\":11640,\"journal\":{\"name\":\"eLife\",\"volume\":\"13 \",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2024-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11563579/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eLife\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.7554/eLife.96425\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eLife","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.7554/eLife.96425","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
肉芽肿的定义是存在有组织的免疫细胞层,其中包括巨噬细胞。肉芽肿通常被描述为免疫系统遏制感染并防止其扩散的一种方式。我们最近建立了一种小鼠感染模型,在这种模型中,暴力色杆菌会诱导先天性免疫系统在肝脏中形成肉芽肿。这种反应成功地消灭了细菌并使肝脏恢复平衡。在这里,我们试图描述参与引导免疫细胞形成肉芽肿不同层次的趋化因子的特征。我们利用空间转录组学研究了肉芽肿反应中所有 CC 和 CXC 趋化因子及其受体的时空表达。随着肉芽肿的成熟和消退,其表达谱随时间和空间发生动态变化。为了研究单核细胞衍生的巨噬细胞在这种免疫反应中的重要性,我们研究了 CCR2 在小鼠感染 C. violaceum 期间的作用。Ccr2-/-小鼠的巨噬细胞数量几乎可以忽略不计,但在C. violaceum感染的病灶中却有大量的中性粒细胞。此外,病变组织结构异常,导致细菌失去抑制作用。如果没有 CCR2,细菌就会扩散,小鼠就会死于感染。这表明,巨噬细胞是成功形成先天性肉芽肿以应对暴风杆菌的关键。
Chemokine expression profile of an innate granuloma.
Granulomas are defined by the presence of organized layers of immune cells that include macrophages. Granulomas are often characterized as a way for the immune system to contain an infection and prevent its dissemination. We recently established a mouse infection model where Chromobacterium violaceum induces the innate immune system to form granulomas in the liver. This response successfully eradicates the bacteria and returns the liver to homeostasis. Here, we sought to characterize the chemokines involved in directing immune cells to form the distinct layers of a granuloma. We use spatial transcriptomics to investigate the spatial and temporal expression of all CC and CXC chemokines and their receptors within this granuloma response. The expression profiles change dynamically over space and time as the granuloma matures and then resolves. To investigate the importance of monocyte-derived macrophages in this immune response, we studied the role of CCR2 during C. violaceum infection. Ccr2-/- mice had negligible numbers of macrophages, but large numbers of neutrophils, in the C. violaceum-infected lesions. In addition, lesions had abnormal architecture resulting in loss of bacterial containment. Without CCR2, bacteria disseminated and the mice succumbed to the infection. This indicates that macrophages are critical to form a successful innate granuloma in response to C. violaceum.
期刊介绍:
eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as:
Research Articles: Detailed reports of original research findings.
Short Reports: Concise presentations of significant findings that do not warrant a full-length research article.
Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research.
Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field.
Scientific Correspondence: Short communications that comment on or provide additional information related to published articles.
Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.