Author:
Lewis Sarah,Singh Dave,Evans Carol E
Abstract
Abstract
Background
Inhalation of particulates is a leading cause of the development of lung diseases and current understanding of the complex relationship between lung metabolism and airborne particulates is incomplete. It is well established that mechanical load is important in the development of the lung and in lung cell differentiation. The interaction between particle exposure and physical forces on alveolar macrophages is a physiologically relevant issue, but as yet understudied. This study examines the effect of cyclic hydrostatic pressure and cotton particles on synthesis of cytokines by human alveolar macrophages.
Methods
Alveolar macrophages were obtained from patients with lung disease, either from lavage samples or from lung tissue resection. The commonly used cell line THP-1 was included in the experiments. Cell cultures were exposed to cotton particles and/cyclic hydrostatic pressure (3 or 5 psi); control cultures were exposed to medium only. TNFα, IL-1β and IL-6 were assayed in the culture media using specific ELISAs. Cells were characterized using morphology and markers specific for macrophages (Jenner/Giemsa staining, CD14 and CD68).
Results
Exposure to cotton particles stimulated cytokine synthesis by macrophages from all three sources; exposure to cyclic hydrostatic pressure alone did not stimulate cytokine synthesis significantly. However, the combination of both particles and cyclic hydrostatic pressure increased the simulation of cytokine synthesis still further. Cell characterization demonstrated that the large majority of cells had a macrophage morphology and were positive for CD14 and CD68.
Conclusion
These data suggest an interaction between cyclic hydrostatic pressure and particulate exposure, which increases alveolar macrophage cytokine production. This interaction was only observed at the higher cyclic hydrostatic pressure. However, in patient samples, there was considerable variation in the amount by which secretion of an individual cytokine increased and there was also variation in the mechanosensitivity of cells from the three different sources. Cyclic hydrostatic pressure, therefore, may be an important modulator of the response of alveolar macrophages to cotton particles, but the source of the cells may be a confounding factor which demands further investigation.
Publisher
Springer Science and Business Media LLC
Reference32 articles.
1. Sanchez-Esteban J, Tsai SW, Sang JB, Qin J, Torday JS, Rubin LP: Effects of mechanical force on lung-specific gene expression.
Am J Med Sci 1998, 3:200–04.
2. Torday JS, Sanchez-Esteban J, Rubin LP: Paracrine mediators of mechanotransduction in lung development.
Am J Med Sci 1998, 316:205–8.
3. Torday JS, Rehan VK: Mechanotransduction determines the structure and function of lung and bone – A theoretical model for the pathophysiology of chronic disease.
Cell Biochem Biophys 2003, 37:235–46.
4. Liu MA, Souza P, Tanswell B, Tanswell AK, Post M: The effect of mechanical strain on fetal rat lung cell proliferation: Comparison of two- and three-dimensional culture systems.
In Vitro Cell Dev Biol Anim. 1995,31(11):858–866.
5. Liu MA, Qin Y, Liu J, Tanswell AK, Post M: Mechanical strain induces pp60
src
activation and translocation to cytoskeleton in fetal rat lung cells.
J Biol Chem 1996, 271:7066–71.
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