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过敏性气道炎症中诱导型和固有型肥大细胞的谱系特异性调控。

Lineage-specific regulation of inducible and constitutive mast cells in allergic airway inflammation.

机构信息

Jeff and Penny Vinik Center for Allergic Disease Research, Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, MA.

Department of Medicine, Harvard Medical School, Boston, MA.

出版信息

J Exp Med. 2021 Jan 4;218(1). doi: 10.1084/jem.20200321.

Abstract

Murine mast cells (MCs) contain two lineages: inducible bone marrow-derived mucosal MCs (MMCs) and constitutive embryonic-derived connective tissue MCs (CTMCs). Here, we use RNA sequencing, flow cytometry, and genetic deletion in two allergic lung inflammation models to define these two lineages. We found that inducible MCs, marked by β7 integrin expression, are highly distinct from airway CTMCs at rest and during inflammation and unaffected by targeted CTMC deletion. β7High MCs expand and mature during lung inflammation as part of a TGF-β-inducible transcriptional program that includes the MMC-associated proteases Mcpt1 and Mcpt2, the basophil-associated protease Mcpt8, granule components, and the epithelial-binding αE integrin. In vitro studies using bone marrow-derived MCs (BMMCs) identified a requirement for SCF in this this TGF-β-mediated development and found that epithelial cells directly elicit TGF-β-dependent BMMC up-regulation of mMCP-1 and αE integrin. Thus, our findings characterize the expansion of a distinct inducible MC subset in C57BL/6 mice and highlight the potential for epithelium to direct MMC development.

摘要

鼠类肥大细胞(MCs)包含两个谱系:诱导性骨髓衍生的黏膜 MCs(MMCs)和组成性胚胎衍生的结缔组织 MCs(CTMCs)。在这里,我们使用 RNA 测序、流式细胞术和两种过敏性肺炎症模型中的基因缺失来定义这两个谱系。我们发现,由β7 整联蛋白表达标记的诱导性 MCs 在静止和炎症期间与气道 CTMCs 高度不同,并且不受靶向 CTMC 缺失的影响。β7High MCs 在肺炎症期间扩增和成熟,作为 TGF-β诱导的转录程序的一部分,该程序包括与 MMC 相关的蛋白酶 Mcpt1 和 Mcpt2、嗜碱性粒细胞相关的蛋白酶 Mcpt8、颗粒成分和上皮结合的 αE 整联蛋白。使用骨髓来源的 MCs(BMMCs)进行的体外研究确定了 SCF 在这种 TGF-β介导的发育中的需求,并发现上皮细胞直接引发 TGF-β依赖性 BMMC 对 mMCP-1 和 αE 整联蛋白的上调。因此,我们的研究结果描述了 C57BL/6 小鼠中一个独特的诱导性 MC 亚群的扩增,并强调了上皮细胞指导 MMC 发育的潜力。

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