Die Rolle von Cathelizidin und des Transkriptionsfaktors NF-kB bei Asthma und COPD

Frank Friedhelm Klescz, Bals, Robert (Prof. Dr. Dr.), Innere Medizin
2011
Asthma and chronic obstructive pulmonary disease (COPD) are two complex diseases of the lung. Asthma as well as COPD have a strong inflammatory component in which different parts of the immune system and the lung are involved. NF-κB is an important transcription factor which controls the expression of many immune genes. Antimicrobial peptides are effector molecules of innate immunity and involved in host defense and inflammation. Since cathelicidins have antimicrobial as well as immunmodulatory
more » ... functions they could also be involved in asthma and COPD. The aim of the present study was to evaluate the role of the murine cathelicidin CRAMP and the transcription factor NF-κB in asthma and COPD. Analysis of the bronchoalveolar lavage (BAL), lung cytokines and serum-IgE showed that cathelicidin plays no role in experimentally induced acute asthma. In the model of chronic asthma, cathelicidin had a complex effect since CRAMP-/- mice had a slightly higher total cell count and more eosinophils in their BAL than wildtype (WT) mice but the load of serum-IgE and TH2 cytokines in the lungs of serum-IgE of CRAMP-/- mice was lower than in WT mice after experimental induced acute asthma. During short-term exposure to cigarette smoke CRAMP had an anti-inflammatory effect as the BAL of CRAMP-/- mice contained more cytokines than identically treated wild type mice. In the chronic COPD model, CRAMP also had an anti-inflammatory effect since the BAL of CRAMP-/- mice contained more cells and more cytokines than identically treated wild type mice. In experimental acute asthma, this work showed that the p65-mediated NF-κB signaling pathway plays an important role. Activation of p65-mediated myeloid NF-κB resulted in an neutrophilic phenotype and had a partly anti-inflammatory effect contrary to a constitutive inhibition of the p65-mediated myeloid NF-κB signaling pathway leading to a partly proinflammatory effect. During short-term exposure to cigarette smoke the p65-mediated NF-κB signaling pathway played no role regarding the inves [...]
doi:10.17192/z2010.0245 fatcat:ej2eyr5yrje5vmliyythexbtye