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髓过氧化物酶在免疫调节、组织炎症和癌症中的非经典功能。

Non-Canonical Functions of Myeloperoxidase in Immune Regulation, Tissue Inflammation and Cancer.

机构信息

Department of Pathology, Feinberg School of Medicine, Northwestern University, 300 East Superior St., Chicago, IL 60611, USA.

出版信息

Int J Mol Sci. 2022 Oct 14;23(20):12250. doi: 10.3390/ijms232012250.

Abstract

Myeloperoxidase (MPO) is one of the most abundantly expressed proteins in neutrophils. It serves as a critical component of the antimicrobial defense system, facilitating microbial killing via generation of reactive oxygen species (ROS). Interestingly, emerging evidence indicates that in addition to the well-recognized canonical antimicrobial function of MPO, it can directly or indirectly impact immune cells and tissue responses in homeostatic and disease states. Here, we highlight the emerging non-canonical functions of MPO, including its impact on neutrophil longevity, activation and trafficking in inflammation, its interactions with other immune cells, and how these interactions shape disease outcomes. We further discuss MPO interactions with barrier forming endothelial and epithelial cells, specialized cells of the central nervous system (CNS) and its involvement in cancer progression. Such diverse function and the MPO association with numerous inflammatory disorders make it an attractive target for therapies aimed at resolving inflammation and limiting inflammation-associated tissue damage. However, while considering MPO inhibition as a potential therapy, one must account for the diverse impact of MPO activity on various cellular compartments both in health and disease.

摘要

髓过氧化物酶(MPO)是中性粒细胞中表达最丰富的蛋白质之一。它作为抗菌防御系统的关键组成部分,通过生成活性氧(ROS)来促进微生物的杀伤。有趣的是,新出现的证据表明,除了 MPO 公认的经典抗菌功能外,它还可以直接或间接地影响稳态和疾病状态下免疫细胞和组织的反应。在这里,我们强调 MPO 新出现的非经典功能,包括其对中性粒细胞寿命、炎症中激活和迁移的影响,它与其他免疫细胞的相互作用,以及这些相互作用如何影响疾病结局。我们还进一步讨论了 MPO 与形成屏障的内皮细胞和上皮细胞、中枢神经系统(CNS)的特化细胞以及它在癌症进展中的作用之间的相互作用。这种多样化的功能以及 MPO 与许多炎症性疾病的关联,使其成为治疗炎症和限制炎症相关组织损伤的潜在目标。然而,在考虑将 MPO 抑制作为一种潜在的治疗方法时,必须考虑 MPO 活性对健康和疾病中各种细胞区室的多样化影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1441/9603794/1a71355e9f81/ijms-23-12250-g001.jpg

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