Substance P Potentiates TGF-1 Production in Lung Epithelial Cell Lines

Abstract

Transforming growth factor-beta (TGF-β) is one of the most important cytokines implicated in growth, differentiation, repair and also the pathogenesis of the lung fibrosis by its stimulatory effect on extracellular matrix deposition. Pulmonary epithelial cells are considered as a source of TGF-β in lung. Substance P (SP), as a neuroimmunomodulator has elevated levels in inflamed airways and although it has significant role in the pathogenesis of the lung fibrosis, but its effect on transforming growth factor -beta (TGF-β) production of the lung epithelial cells (and so its regulatory potential) remains unclear.
In this study TGF-1 levels in supernatants of the normal (BEAS-2B) and cancerous (A549) lung epithelial cell line cultures at the presence of various concentrations of SP were examined and MTT assay was performed to evaluate cells viability.
We have observed that SP (without any other stimulator) significantly augments TGF-β production of both BEAS and A54 cells and this effect is inhibited by NK1-receptor antagonist (CP-96345). We have also observed that the viability of cells did not significantly affect at the presence of SP.
It can be concluded that SP can directly modulate the release of TGF-β from human bronchial epithelial cell line and thereby participates in various lung functions or pathologic conditions.