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Published on: April 16, 2019
Bronchial epithelial cells release chemotactic activity for lymphocytes
R A Robbins1, S Shoji, J Linder
1Research Service, Omaha Veterans Administration Medical Center, Omaha, Nebraska 68105.
Insights
Bronchial epithelial cells release lymphocyte-attracting factors, influencing local immune cell populations. These findings highlight a novel mechanism in immune cell recruitment to lung tissues.
Area of Science:
- Immunology
- Cell Biology
- Respiratory Medicine
Background:
- Lymphocytes are often found near bronchial tissues.
- A potential mechanism involves bronchial epithelial cells releasing lymphocyte-attracting substances.
Purpose of the Study:
- To investigate if bovine bronchial epithelial cells secrete factors that attract lymphocytes.
- To characterize the nature of these chemotactic factors and the types of lymphocytes attracted.
Main Methods:
- Culturing bovine bronchial epithelial cells in serum-free media.
- Assessing supernatant chemotactic activity using blind-well chambers and checkerboard analysis.
- Characterizing factor properties (solubility, heat/trypsin sensitivity) and lymphocyte subsets via monoclonal antibody staining and molecular sieve chromatography.
Main Results:
- Supernatants from bronchial epithelial cell cultures significantly attracted more lymphocytes than control media.
- The activity was dose-dependent and confirmed as chemotactic.
- Factors were partially inactivated by heat and trypsin, and not ethyl acetate-extractable.
- Responding lymphocytes were mainly T-helper cells, with some B-lymphocytes.
- Chromatography identified multiple chemotactic peaks, some specific to T-helper or B-lymphocytes.
Conclusions:
- Bronchial epithelial cells actively release lymphocyte chemotactic factors.
- These cells play a role in modulating the local immune cell environment within the airways.
- This suggests a mechanism for immune cell recruitment and regulation in the respiratory tract.
Abstract:
Lymphocytes can frequently be observed in association with bronchial tissues. One mechanism that might account for this association is that bronchial epithelial cells might release chemotactic factors for lymphocytes. To test this hypothesis, bovine bronchial epithelial cells were cultured in serum-free media, and the supernatant fluids were harvested and evaluated for lymphocyte chemotactic activity using a blind-well chamber technique. Media alone attracted few lymphocytes (12 +/- 2 cells/high power field), but in contrast, there was a significant increase in the number of cells attracted by supernatant fluids obtained from bronchial epithelial cell cultures (40 +/- 6 cells/high power field, P = 0.002). The activity was dose dependent and was demonstrated to be chemotactic activity by checkerboard analysis. Partial characterization of the activity revealed it was not extractable into ethyl acetate but was partially inactivated by trypsin and heat (100 degrees C, 15 min). The responding cells were predominantly T-helper lymphocytes as shown by monoclonal antibody staining, with a smaller proportion being B-lymphocytes. Molecular sieve column chromatography revealed multiple peaks of lymphocyte chemotactic activity, with three of the peaks preferentially attracting T-helper lymphocytes and one of the peaks preferentially attracting B-lymphocytes. These data demonstrate that bronchial epithelial cells can release chemotactic factors for lymphocytes and suggest that bronchial epithelial cells may modulate their local population of immune effector cells.
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