Presence of substance P and neurokinin 1 receptors in human sputum macrophages and U-937 cells

Citation
Pr. Germonpre et al., Presence of substance P and neurokinin 1 receptors in human sputum macrophages and U-937 cells, EUR RESP J, 14(4), 1999, pp. 776-782
Citations number
31
Categorie Soggetti
Cardiovascular & Respiratory Systems","da verificare
Journal title
EUROPEAN RESPIRATORY JOURNAL
ISSN journal
09031936 → ACNP
Volume
14
Issue
4
Year of publication
1999
Pages
776 - 782
Database
ISI
SICI code
0903-1936(199910)14:4<776:POSPAN>2.0.ZU;2-K
Abstract
Tachykinins such as substance P (SP) may be involved in the pathogenesis of inflammatory airway diseases such as asthma, This study investigated the p resence of SP and its receptor in the differentiated macrophagelike U-937 c ell Line and in macrophages from sputum induced in healthy subjects (n=8). In situ hybridization with digoxigenin-labelled sense and antisense complem entary ribonucleic acid (cRNA) probes was used to determine the expression of SP and its receptor (neurokinin (NK)(1) receptor). SP-immunoreactive mat erial was detected using a rabbit anti-SP antiserum and the alkaline phosph atase anti-alkaline phosphatase technique. beta-preprotachykinin (PPT)-I messenger ribonucleic acid (mRNA) encoding SP , was detected using in situ hybridization in differentiated U-937 cells as well as in CD45+ human leukocyte antigen (HLA) DR+ sputum macrophages. The expression of the PPT-I mRNA was increased in lipopolysaccharide (LPS)-sti mulated U-937 cells. beta-immunoreactive material was found in differentiat ed U-937 cells and in CD68+ sputum macrophages. NK1 receptor mRNA was detec ted in differentiated U-937 cells and sputum macrophages. Incubation of U-9 37 cells with SP considerably increased the expression of NK1 receptor mRNA . This study demonstrates that human monocytes/macrophages express substance P and that this expression is upregulated by lipopolysacharide. Human monoc ytes/macrophages also express neurokinin(1) receptor messenger ribonucleic acid, suggesting an autocrine effect of substance P on these cells.