Surfactant Lipids at the Host-Environment Interface Metabolic Sensors, Suppressors, and Effectors of Inflammatory Lung Disease

被引:108
作者
Fessler, Michael B. [1 ]
Summer, Ross S. [2 ,3 ]
机构
[1] NIEHS, Immun Inflammat & Dis Lab, NIH, 111 TW Alexander Dr,POB 12233,Maildrop D2-01, Res Triangle Pk, NC 27709 USA
[2] Thomas Jefferson Univ, Ctr Translat Med, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Jane & Leonard Korman Lung Ctr, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
lung; surfactant; phospholipid; cholesterol; innate immunity; RESPIRATORY-DISTRESS-SYNDROME; LOW-DENSITY-LIPOPROTEIN; MASS-SPECTROMETRIC CHARACTERIZATION; PHOSPHOLIPID OXIDATION-PRODUCTS; SYNCYTIAL VIRUS-INFECTION; ALVEOLAR LINING MATERIAL; LPS-BINDING PROTEIN; OXIDIZED PHOSPHOLIPIDS; EPITHELIAL-CELLS; INNATE IMMUNITY;
D O I
10.1165/rcmb.2016-0011PS
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lipid composition of pulmonary surfactant is unlike that of any other body fluid. This extracellular lipid reservoir is also uniquely susceptible by virtue of its direct and continuous exposure to environmental oxidants, inflammatory agents, and pathogens. Historically, the greatest attention has been focused on those biophysical features of surfactant that serve to reduce surface tension at the air-liquid interface. More recently, surfactant lipids have also been recognized as bioactive molecules that maintain immune quiescence in the lung but can also be remodeled by the inhaled environment into neolipids that mediate key roles in inflammation, immunity, and fibrosis. This review focuses on the roles in inflammatory and infectious lung disease of two classes of native surfactant lipids, glycerophospholipids and sterols, and their corresponding oxidized species, oxidized glycerophospholipids and oxysterols. We highlight evidence that surfactant composition is sensitive to circulating lipoproteins and that the lipid milieu of the alveolus should thus be recognized as susceptible to diet and common systemic metabolic disorders. We also discuss intriguing evidence suggesting that oxidized surfactant lipids may represent an evolutionary link between immunity and tissue homeostasis that arose in the primordial lung. Taken together, the emerging picture is one in which the unique environmental susceptibility of the lung, together with its unique extracellular lipid requirements, may have made this organ both an evolutionary hub and an engine for lipid-immune cross-talk.
引用
收藏
页码:624 / 635
页数:12
相关论文
共 132 条
[21]   Phospholipid oxidation generates potent anti-inflammatory lipid mediators that mimic structurally related pro-resolving eicosanoids by activating Nrf2 [J].
Bretscher, Peter ;
Egger, Julian ;
Shamshiev, Abdijapar ;
Troetzmueller, Martin ;
Koefeler, Harald ;
Carreira, Erick M. ;
Kopf, Manfred ;
Freigang, Stefan .
EMBO MOLECULAR MEDICINE, 2015, 7 (05) :593-607
[22]   ANTI-PHOSPHORYLCHOLINE ANTIBODIES OF THE T15 IDIOTYPE ARE OPTIMALLY PROTECTIVE AGAINST STREPTOCOCCUS-PNEUMONIAE [J].
BRILES, DE ;
FORMAN, C ;
HUDAK, S ;
CLAFLIN, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (04) :1177-1185
[23]   The molecular basis of pulmonary alveolar proteinosis [J].
Carey, Brenna ;
Trapnell, Bruce C. .
CLINICAL IMMUNOLOGY, 2010, 135 (02) :223-235
[24]   C-reactive protein binds to both oxidized LDL and apoptotic cells through recognition of a common ligand: Phosphorylcholine of oxidized phospholipids [J].
Chang, MK ;
Binder, CJ ;
Torzewski, M ;
Witztum, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :13043-13048
[25]   Monoclonal antibodies against oxidized low-density lipoprotein bind to apoptotic cells and inhibit their phagocytosis by elicited macrophages:: Evidence that oxidation-specific epitopes mediate macrophage recognition [J].
Chang, MK ;
Bergmark, C ;
Laurila, A ;
Hörkkö, S ;
Han, KH ;
Friedman, P ;
Dennis, EA ;
Witztum, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) :6353-6358
[26]   Enhancement of enveloped virus entry by phosphatidylserine [J].
Coil, DA ;
Miller, AD .
JOURNAL OF VIROLOGY, 2005, 79 (17) :11496-11500
[27]  
COONROD JD, 1983, J IMMUNOL, V130, P2589
[28]   CHARACTERIZATION OF THE EXTRACELLULAR BACTERICIDAL FACTORS OF RAT ALVEOLAR LINING MATERIAL [J].
COONROD, JD ;
LESTER, RL ;
HSU, LC .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (04) :1269-1279
[29]   Host-derived oxidized phospholipids and HDL regulate innate immunity in human leprosy [J].
Cruz, Daniel ;
Watson, Andrew D. ;
Miller, Christopher S. ;
Montoya, Dennis ;
Ochoa, Maria-Teresa ;
Sieling, Peter A. ;
Gutierrez, Miguel A. ;
Navab, Mohamad ;
Reddy, Srinivasa T. ;
Witztum, Joseph L. ;
Fogelman, Alan M. ;
Rea, Thomas H. ;
Eisenberg, David ;
Berliner, Judith ;
Modlin, Robert L. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (08) :2917-2928
[30]   Protection against inhaled oxidants through scavenging of oxidized lipids by macrophage receptors MARCO and SR-AI/II [J].
Dahl, Morten ;
Bauer, Alison K. ;
Arredouani, Mohamed ;
Soininen, Raija ;
Tryggvason, Karl ;
Kleeberger, Steven R. ;
Kobzik, Lester .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (03) :757-764