Neutrophils in innate immunity and systems biology-level approaches

被引:42
作者
Rungelrath, Viktoria [1 ]
Kobayashi, Scott D. [1 ]
DeLeo, Frank R. [1 ]
机构
[1] NIAID, Bacteriol Lab, Rocky Mt Labs, NIH, Hamilton, MT 59840 USA
关键词
apoptosis; granulopoiesis; inflammation; microarray; neutrophil; phagocytosis; systems biology; transcriptome; APOPTOSIS-DIFFERENTIATION PROGRAM; COLONY-STIMULATING FACTOR; NECROSIS-FACTOR-ALPHA; HUMAN POLYMORPHONUCLEAR LEUKOCYTES; EARLY TRANSCRIPTIONAL RESPONSE; CHRONIC GRANULOMATOUS-DISEASE; SINGLE-CELL TRANSCRIPTOMICS; FACTOR GM-CSF; GENE-EXPRESSION; RESPIRATORY BURST;
D O I
10.1002/wsbm.1458
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The innate immune system is the first line of host defense against invading microorganisms. Polymorphonuclear leukocytes (PMNs or neutrophils) are the most abundant leukocyte in humans and essential to the innate immune response against invading pathogens. Compared to the acquired immune response, which requires time to develop and is dependent on previous interaction with specific microbes, the ability of neutrophils to kill microorganisms is immediate, nonspecific, and not dependent on previous exposure to microorganisms. Historically, studies of PMN-pathogen interaction focused on the events leading to killing of microorganisms, such as recruitment/chemotaxis, transmigration, phagocytosis, and activation, whereas postphagocytosis sequelae were infrequently considered. In addition, it was widely accepted that human neutrophils possessed limited capacity for new gene transcription and thus, relatively little biosynthetic capacity. This notion has changed dramatically within the past 20 years. Further, there is now more effort directed to understand the events occurring in PMNs after killing of microbes. Herein, we give an updated review of the systems biology-level approaches that have been used to gain an enhanced view of the role of neutrophils during host-pathogen interaction and neutrophil-mediated diseases. We anticipate that these and future systems-level studies will continue to provide information important for understanding, treatment, and control of diseases caused by pathogenic microorganisms.
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页数:30
相关论文
共 246 条
[1]   Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens [J].
Ackerman, AL ;
Kyritsis, C ;
Tampé, R ;
Cresswell, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12889-12894
[2]   KINETICS OF HUMAN HEMATOPOIETIC-CELLS AFTER INVIVO ADMINISTRATION OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR [J].
AGLIETTA, M ;
PIACIBELLO, W ;
SANAVIO, F ;
STACCHINI, A ;
APRA, F ;
SCHENA, M ;
MOSSETTI, C ;
CARNINO, F ;
CALIGARISCAPPIO, F ;
GAVOSTO, F .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (02) :551-557
[3]  
ALBRECHTSEN M, 1988, IMMUNOLOGY, V64, P201
[4]   p38-MAPK signals survival by phosphorylation of caspase-8 and caspase-3 in human neutrophils [J].
Alvarado-Kristensson, M ;
Melander, F ;
Leandersson, K ;
Rönnstrand, L ;
Wernstedt, C ;
Andersson, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (04) :449-458
[5]   LEUKOKINETIC STUDIES .4. TOTAL BLOOD, CIRCULATING AND MARGINAL GRANULOCYTE POOLS AND GRANULOCYTE TURNOVER RATE IN NORMAL SUBJECTS [J].
ATHENS, JW ;
WINTROBE, MM ;
ASHENBRUCKER, H ;
CARTWRIGHT, GE ;
MAUER, AM ;
HAAB, OP ;
RAAB, SO .
JOURNAL OF CLINICAL INVESTIGATION, 1961, 40 (06) :989-&
[6]   Tumor necrosis factor-α activation of the c-Jun N-terminal kinase pathway in human neutrophils [J].
Avdi, NJ ;
Nick, JA ;
Whitlock, BB ;
Billstrom, MA ;
Henson, PM ;
Johnson, GL ;
Worthen, GS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (03) :2189-2199
[7]   Pathogen Cell-to-Cell Variability Drives Heterogeneity in Host Immune Responses [J].
Avraham, Roi ;
Haseley, Nathan ;
Brown, Douglas ;
Penaranda, Cristina ;
Jijon, Humberto B. ;
Trombetta, John J. ;
Satija, Rahul ;
Shalek, Alex K. ;
Xavier, Ramnik J. ;
Regev, Aviv ;
Hung, Deborah T. .
CELL, 2015, 162 (06) :1309-1321
[8]   DEVELOPMENT OF NEUTROPHILIC POLYMORPHONUCLEAR LEUKOCYTES IN HUMAN BONE MARROW - ORIGIN AND CONTENT OF AZUROPHIL AND SPECIFIC GRANULES [J].
BAINTON, DF ;
ULLYOT, JL ;
FARQUHAR, MG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1971, 134 (04) :907-+
[9]   Cutting edge:: Infection by the agent of human granulocytic ehrlichiosis prevents the respiratory burst by down-regulating gp91phox1 [J].
Banerjee, R ;
Anguita, J ;
Roos, D ;
Fikrig, E .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :3946-3949
[10]   NLRP3 Inflammasome Activity Is Negatively Controlled by miR-223 [J].
Bauernfeind, Franz ;
Rieger, Anna ;
Schildberg, Frank A. ;
Knolle, Percy A. ;
Schmid-Burgk, Jonathan L. ;
Hornung, Veit .
JOURNAL OF IMMUNOLOGY, 2012, 189 (08) :4175-4181