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Neutrophil apoptosis and the resolution of infection

期刊

IMMUNOLOGIC RESEARCH
卷 43, 期 1-3, 页码 25-61

出版社

HUMANA PRESS INC
DOI: 10.1007/s12026-008-8049-6

关键词

Neutrophil; Cell death; Apoptosis; Phagocytosis; Pyroptosis; Autophagy; Macrophage; Inflammation; Pathogen; Innate immunity

资金

  1. National Institute of Allergy and Infectious Diseases
  2. National Institutes of Health
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [ZIAAI000900, Z01AI000900] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Polymorphonuclear leukocytes (PMNs) are the most abundant white cell in humans and an essential component of the innate immune system. PMNs are typically the first type of leukocyte recruited to sites of infection or areas of inflammation. Ingestion of microorganisms triggers production of reactive oxygen species and fusion of cytoplasmic granules with forming phagosomes, leading to effective killing of ingested microbes. Phagocytosis of bacteria typically accelerates neutrophil apoptosis, which ultimately promotes the resolution of infection. However, some bacterial pathogens alter PMN apoptosis to survive and thereby cause disease. Herein, we review PMN apoptosis and the ability of microorganisms to alter this important process.

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