Regulation of alveolar macrophage death in acute lung inflammation

被引:265
作者
Fan, Erica K. Y. [1 ]
Fan, Jie [2 ,3 ,4 ]
机构
[1] Univ Pittsburgh, Kenneth P Dietrich Sch Arts & Sci, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Surg, Sch Med, Pittsburgh, PA 15213 USA
[3] Vet Affairs Pittsburgh Healthcare Syst, Res & Dev, Pittsburgh, PA 15240 USA
[4] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15219 USA
来源
RESPIRATORY RESEARCH | 2018年 / 19卷
基金
美国国家卫生研究院;
关键词
Acute lung injury; Macrophages; Cell death; Pyroptosis; Necroptosis; Autophagy; MIXED LINEAGE KINASE; PROGRAMMED CELL-DEATH; DOMAIN-LIKE PROTEIN; RESPIRATORY-DISTRESS-SYNDROME; MULTIPLE ORGAN FAILURE; ISCHEMIA-REPERFUSION INJURY; HEMORRHAGIC-SHOCK PRIMES; NECROPTOSIS IN-VIVO; SEVERE BLUNT TRAUMA; TLR2; UP-REGULATION;
D O I
10.1186/s12931-018-0756-5
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Acute lung injury (ALI) and its severe form, known as acute respiratory distress syndrome (ARDS), are caused by direct pulmonary insults and indirect systemic inflammatory responses that result from conditions such as sepsis, trauma, and major surgery. The reciprocal influences between pulmonary and systemic inflammation augments the inflammatory process in the lung and promotes the development of ALI. Emerging evidence has revealed that alveolar macrophage (AM) death plays important roles in the progression of lung inflammation through its influence on other immune cell populations in the lung. Cell death and tissue inflammation form a positive feedback cycle, ultimately leading to exaggerated inflammation and development of disease. Pharmacological manipulation of AM death signals may serve as a logical therapeutic strategy for ALI/ARDS. This review will focus on recent advances in the regulation and underlying mechanisms of AM death as well as the influence of AM death on the development of ALI.
引用
收藏
页数:13
相关论文
共 144 条
[1]  
ABRAHAM E, 1988, CIRC SHOCK, V25, P33
[2]   SIGNALING ACTIVATED BY THE DEATH RECEPTORS OF THE TNFR FAMILY [J].
Andera, Ladislav .
BIOMEDICAL PAPERS-OLOMOUC, 2009, 153 (03) :173-180
[3]   HMGB1 Is a Therapeutic Target for Sterile Inflammation and Infection [J].
Andersson, Ulf ;
Tracey, Kevin J. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 29, 2011, 29 :139-162
[4]  
ASHBAUGH DG, 1967, LANCET, V2, P319
[5]   cIAP1 and cIAP2 facilitate cancer cell survival by functioning as E3 ligases that promote RIP1 ubiquitination [J].
Bertrand, Mathieu J. M. ;
Milutinovic, Snezana ;
Dickson, Kathleen M. ;
Ho, Wai Chi ;
Boudreault, Alain ;
Durkin, Jon ;
Gillard, John W. ;
Jaquith, James B. ;
Morris, Stephen J. ;
Barker, Philip A. .
MOLECULAR CELL, 2008, 30 (06) :689-700
[6]   The Adaptor Protein FADD Protects Epidermal Keratinocytes from Necroptosis In Vivo and Prevents Skin Inflammation [J].
Bonnet, Marion C. ;
Preukschat, Daniela ;
Welz, Patrick-Simon ;
van Loo, Geert ;
Ermolaeva, Maria A. ;
Bloch, Wilhelm ;
Haase, Ingo ;
Pasparakis, Manolis .
IMMUNITY, 2011, 35 (04) :572-582
[7]   Gain-of-Function Pyrin Mutations Induce NLRP3 Protein-Independent Interleukin-1β Activation and Severe Autoinflammation in Mice [J].
Chae, Jae Jin ;
Cho, Young-Hun ;
Lee, Geun-Shik ;
Cheng, Jun ;
Liu, P. Paul ;
Feigenbaum, Lionel ;
Katz, Stephen I. ;
Kastner, Daniel L. .
IMMUNITY, 2011, 34 (05) :755-768
[8]   Translocation of mixed lineage kinase domain-like protein to plasma membrane leads to necrotic cell death [J].
Chen, Xin ;
Li, Wenjuan ;
Ren, Junming ;
Huang, Deli ;
He, Wan-ting ;
Song, Yunlong ;
Yang, Chao ;
Li, Wanyun ;
Zheng, Xinru ;
Chen, Pengda ;
Han, Jiahuai .
CELL RESEARCH, 2014, 24 (01) :105-121
[9]   Phosphorylation-Driven Assembly of the RIP1-RIP3 Complex Regulates Programmed Necrosis and Virus-Induced Inflammation [J].
Cho, YoungSik ;
Challa, Sreerupa ;
Moquin, David ;
Genga, Ryan ;
Ray, Tathagat Dutta ;
Guildford, Melissa ;
Chan, Francis Ka-Ming .
CELL, 2009, 137 (06) :1112-1123
[10]   Pronecrotic mixed lineage kinase domain-like protein expression is a prognostic biomarker in patients with early-stage resected pancreatic adenocarcinoma [J].
Colbert, Lauren E. ;
Fisher, Sarah B. ;
Hardy, Claire W. ;
Hall, William A. ;
Saka, Burcu ;
Shelton, Joseph W. ;
Petrova, Aleksandra V. ;
Warren, Matthew D. ;
Pantazides, Brooke G. ;
Gandhi, Khanjan ;
Kowalski, Jeanne ;
Kooby, David A. ;
El-Rayes, Bassel F. ;
Staley, Charles A., III ;
Adsay, N. Volkan ;
Curran, Walter J., Jr. ;
Landry, Jerome C. ;
Maithel, Shishir K. ;
Yu, David S. .
CANCER, 2013, 119 (17) :3148-3155