Human bronchial smooth muscle cells in culture produce stem cell factor

Citation
O. Kassel et al., Human bronchial smooth muscle cells in culture produce stem cell factor, EUR RESP J, 13(5), 1999, pp. 951-954
Citations number
23
Categorie Soggetti
Cardiovascular & Respiratory Systems","da verificare
Journal title
EUROPEAN RESPIRATORY JOURNAL
ISSN journal
09031936 → ACNP
Volume
13
Issue
5
Year of publication
1999
Pages
951 - 954
Database
ISI
SICI code
0903-1936(199905)13:5<951:HBSMCI>2.0.ZU;2-A
Abstract
A mast cell infiltration of the bronchial smooth muscle layer has been repo rted in patients sensitized to common allergens. Stem cell factor (SCF) is a chemotactic and survival factor for mast cells. SCF is expressed as a sol uble (sSCF) and a membrane-bound (mSCF) form, after alternative splicing of the exon encoding the proteolytic cleavage site. SCF expression by human b ronchial smooth muscle cells in culture was evaluated, comparing it to that of human lung fibroblasts in culture. sSCF released in the culture supernatant was assessed by an enzyme-linked i mmunosorbent assay. Total SCF messenger ribonucleic acid (mRNA) was measure d by competitive polymerase chain reaction (PCR) after reverse transcriptio n. Expression of the two forms of SCF mRNA was assessed by PCR, with primer s spanning the alternatively spliced exon. Smooth muscle cells produced sSCF (21.9+/-2.6 pg.mL(-1)), although at lower levels than fibroblasts (35.9+/-3.5 pg.mL(-1)); the expression of total SC F mRNA was also at lower levels than in fibroblasts (8.6+/-0.2 and 19.0+/-2 .0 amol.fmol glyceraldehyde 3-phosphate dehydrogenase complementary deoxyri bonucleic acid(-1), respectively). However, smooth muscle cells expressed p roportionally more (1.7-fold) mSCF mRNA than did fibroblasts. In conclusion, this study shows that bronchial smooth muscle cells express stem cell factor, with a relatively high expression of membrane-bound stem cell factor. This might be related to the presence of mast cells within the bronchial smooth muscle layer, ie. at the site of bronchoconstriction, wit h possible implications in the pathophysiology of asthma.