Organic barn dust inhibits surfactant protein D production through protein kinase-c alpha dependent increase of GPR116

Prolonged exposure to organic barn dusts can lead to chronic inflammation and a broad range of lung problems over time, mediated by innate immune mechanisms. The immune surfactant or collectin surfactant protein D (SP-D) is a crucial multifunctional innate immune receptor. Little work to date has examined the effect of such collectins in response to organic dusts. We provide evidence here that agricultural organic dusts can inhibit mRNA and protein expression of SP-D in a human alveolar epithelial cell line, and an in vivo mouse model. This inhibition was not a result of lipopolysaccharide (LPS) or peptidoglycans, the two most commonly cited immune active components of these dusts. We further show that inhibition of the signaling molecule protein kinase C alpha (PKCα) can reverse this inhibition implicating it as a mechanism of SP-D inhibition. Examination of the SP-D regulatory receptor GPR116 showed that its mRNA expression was increased in response to dust and inhibited by blocking PKCα, implicating it as a means of inhibiting SP-D in the lungs in response to organic dusts. This reduction shows that organic barn dust can reduce lung SP-D, thus leaving workers potentially at risk for a host of pathogens.

[1]  J. Whitsett,et al.  Epithelial Gpr 116 regulates pulmonary alveolar homeostasis via G q / 11 signaling , 2018 .

[2]  J. Whitsett,et al.  Epithelial Gpr116 regulates pulmonary alveolar homeostasis via Gq/11 signaling. , 2017, JCI insight.

[3]  K. Bailey,et al.  Effect of low-level CO2 on innate inflammatory protein response to organic dust from swine confinement barns , 2017, Journal of Occupational Medicine and Toxicology.

[4]  G. Aulakh,et al.  Toll-like receptor 9 partially regulates lung inflammation induced following exposure to chicken barn air , 2016, Journal of Occupational Medicine and Toxicology.

[5]  D. Romberger,et al.  Proteases in agricultural dust induce lung inflammation through PAR-1 and PAR-2 activation. , 2015, American journal of physiology. Lung cellular and molecular physiology.

[6]  D. Romberger,et al.  Shotgun Pyrosequencing Metagenomic Analyses of Dusts from Swine Confinement and Grain Facilities , 2014, PloS one.

[7]  S. Wakana,et al.  Lung Surfactant Levels are Regulated by Ig-Hepta/GPR116 by Monitoring Surfactant Protein D , 2013, PloS one.

[8]  D. Romberger,et al.  Myeloid differentiation factor 88-dependent signaling is critical for acute organic dust-induced airway inflammation in mice. , 2013, American journal of respiratory cell and molecular biology.

[9]  Todd M Umstead,et al.  Essential regulation of lung surfactant homeostasis by the orphan G protein-coupled receptor GPR116. , 2013, Cell reports.

[10]  D. Romberger,et al.  Respiratory Health Effects of Large Animal Farming Environments , 2012, Journal of toxicology and environmental health. Part B, Critical reviews.

[11]  U. Kishore,et al.  An Insight into the Diverse Roles of Surfactant Proteins, SP-A and SP-D in Innate and Adaptive Immunity , 2012, Front. Immun..

[12]  C. Nishitani,et al.  Diverse Functions of Pulmonary Collectins in Host Defense of the Lung , 2012, Journal of biomedicine & biotechnology.

[13]  D. Romberger,et al.  Immunological and inflammatory responses to organic dust in agriculture , 2012, Current opinion in allergy and clinical immunology.

[14]  D. Romberger,et al.  Sequential activation of protein kinase C isoforms by organic dust is mediated by tumor necrosis factor. , 2010, American journal of respiratory cell and molecular biology.

[15]  C. Erridge Endogenous ligands of TLR2 and TLR4: agonists or assistants? , 2010, Journal of leukocyte biology.

[16]  K. Bailey,et al.  Muramic Acid, Endotoxin, 3-Hydroxy Fatty Acids, and Ergosterol Content Explain Monocyte and Epithelial Cell Inflammatory Responses to Agricultural Dusts , 2010, Journal of toxicology and environmental health. Part A.

[17]  Motoko Takahashi,et al.  Pulmonary surfactant protein D binds MD-2 through the carbohydrate recognition domain. , 2008, Biochemistry.

[18]  A. Gow,et al.  S-Nitrosylation of Surfactant Protein-D Controls Inflammatory Function , 2008, PLoS biology.

[19]  K. Bailey,et al.  Toll-like receptor 2 is upregulated by hog confinement dust in an IL-6-dependent manner in the airway epithelium. , 2008, American journal of physiology. Lung cellular and molecular physiology.

[20]  H. Townsend,et al.  ROLE OF TOLL-LIKE RECEPTOR 4 IN LUNG INFLAMMATION FOLLOWING EXPOSURE TO SWINE BARN AIR , 2008, Experimental lung research.

[21]  D. Romberger,et al.  Feedlot dust stimulation of interleukin-6 and -8 requires protein kinase Cε in human bronchial epithelial cells , 2007 .

[22]  S. V. Von Essen,et al.  Environmental and occupational respiratory disorders Repeat organic dust exposure – induced monocyte inflammation is associated with protein kinase C activity , 2017 .

[23]  T. Fukuzawa,et al.  Multiple processing of Ig-Hepta/GPR116, a G protein-coupled receptor with immunoglobulin (Ig)-like repeats, and generation of EGF2-like fragment. , 2006, Journal of biochemistry.

[24]  Tsuyoshi Saito,et al.  Human pulmonary surfactant protein D binds the extracellular domains of Toll-like receptors 2 and 4 through the carbohydrate recognition domain by a mechanism different from its binding to phosphatidylinositol and lipopolysaccharide. , 2006, Biochemistry.

[25]  M. Kamran,et al.  Surfactant proteins SP-A and SP-D: structure, function and receptors. , 2006, Molecular immunology.

[26]  Susan S. Schiffman,et al.  Symptomatic Effects of Exposure to Diluted Air Sampled from a Swine Confinement Atmosphere on Healthy Human Subjects , 2005, Environmental health perspectives.

[27]  J. Nick,et al.  By Binding SIRPα or Calreticulin/CD91, Lung Collectins Act as Dual Function Surveillance Molecules to Suppress or Enhance Inflammation , 2003, Cell.

[28]  S. V. Von Essen,et al.  The respiratory inflammatory response to the swine confinement building environment: the adaptation to respiratory exposures in the chronically exposed worker. , 2003, Journal of agricultural safety and health.

[29]  S. V. Von Essen,et al.  Hog barn dust extract stimulates IL-8 and IL-6 release in human bronchial epithelial cells via PKC activation. , 2002, Journal of applied physiology.

[30]  T. Hartung,et al.  Characteristics of surfactant protein A and D binding to lipoteichoic acid and peptidoglycan, 2 major cell wall components of gram-positive bacteria. , 2001, The Journal of infectious diseases.

[31]  B. Webb,et al.  Protein kinase C isoenzymes: a review of their structure, regulation and role in regulating airways smooth muscle tone and mitogenesis , 2000, British journal of pharmacology.

[32]  D. Voelker,et al.  Surfactant Proteins A and D Bind CD14 by Different Mechanisms* , 2000, The Journal of Biological Chemistry.

[33]  H. Folgering,et al.  Longitudinal changes in bronchial responsiveness associated with swine confinement dust exposure. , 2000, Chest.

[34]  W. Voorhout,et al.  Aerosolized endotoxin is immediately bound by pulmonary surfactant protein D in vivo. , 1999, Biochimica et biophysica acta.

[35]  E. Crouch Structure, biologic properties, and expression of surfactant protein D (SP-D). , 1998, Biochimica et biophysica acta.

[36]  U. Kishore,et al.  A novel method of purifying lung surfactant proteins A and D from the lung lavage of alveolar proteinosis patients and from pooled amniotic fluid. , 1998, Journal of immunological methods.

[37]  L. Palmberg,et al.  Effect of exposure to swine dust on levels of IL-8 in airway lavage fluid. , 1997, Thorax.

[38]  M. Simon,et al.  Subunits βγ of heterotrimeric G protein activate β2 isoform of phospholipase C , 1992, Nature.