Increased IL-17RA and IL-17RC in End-Stage COPD and the Contribution to Mast Cell Secretion of FGF-2 and VEGF
© The Author(s). 2017
Received: 10 February 2017
Accepted: 2 March 2017
Published: 15 March 2017
Mast cells are accumulated in advanced chronic obstructive pulmonary disease (COPD), and interleukin (IL)-17 signaling plays a role in disease progression. The expression, localization and functional relevance of IL-17 receptor (R)A and IL-17RC was explored in COPD by immunodetection, and functional assays.
IL-17RA and IL-17RC was increased in very severe COPD, and expressed by mast cells. Increased secretion of the pro-angiogenic basic fibroblast growth factor and vascular endothelial growth factor was observed in vitro-maintained mast cells stimulated with IL-17A. Expression of these mediators was confirmed in end-stage COPD. Thus, accumulation of mast cells in COPD may contribute to vascular remodeling.
Baseline demographics and clinical characteristics
Smokers w/o COPD
COPD GOLD I
COPD GOLD II-III
COPD GOLD IV
63 ± 4.8
57 ± 3.3
67 ± 2.9
68 ± 1.9
61 ± 1.4
1.64 ± 0.1
1.71 ± 0.1
1.74 ± 0.1
1.73 ± 0.1
1.69 ± 0.1
65 ± 4.6
69 ± 4.6
69 ± 5.7
73 ± 3.1
65 ± 1.7
Body mass index
24 ± 1.3
24 ± 1.0
23 ± 1.2
24 ± 1.1
23 ± 1.0
43 ± 8.2
40 ± 7.6
48 ± 3.3
41 ± 3.9
86 ± 5.7
79 ± 2.0
67 ± 0.9
55 ± 2.8
32 ± 2.0
110 ± 6.2
98 ± 6.0
87 ± 2.3
64 ± 3.1
23 ± 1.4
As not only structural cells displayed immunoreactivity, co-staining techniques for different cellular markers was next performed to determine the specific cell types expressing IL-17RA and IL-17RC in the peripheral lung. In accordance with previous findings, expression was observed across different immune cell populations, including B lymphocytes (Fig. 1h and m), as well as on structural cells. Expression of both IL-17RA and IL-17RC was also detected on tryptase + mast cells (mouse anti-tryptase, Merck-Millipore, Solna, Sweden) (Fig. 1k and p). Previous studies have documented an accumulation of mast cells in lung tissue of patients with advanced COPD , although the role of mast cells in COPD remains elusive. We thus explored the potential functional relevance of IL-17 receptor expression on mast cells in COPD. To this end, CD133+ hematopoietic stem cell progenitors were isolated (n = 5) and differentiated into mast cells, in vitro, as described elsewhere . 105 mast cells were following 4 weeks maturation stimulated for 8 hours with 1000 ng IL-17A (R&D Systems, Minneapolis, MN, USA), or left unstimulated. Lipopolysaccharide (LPS, Sigma-Aldrich) was used as a positive control.
The in vitro-matured cells exhibited surface markers and functionality consistent with in vivo mast cells (i.e. expression of tryptase, chymase, c-kit and FcεR1; data not shown) [4, 5]. In addition, mRNA transcripts of both IL17RA and IL17RC were detected following in vitro-maturation (data not shown), supporting a phenotypic resemblance to pulmonary mast cells. To evaluate the potential contribution of IL-17A responsive mast cells to the pathology of COPD, we assessed the secretion of proteins associated with COPD by multiplex laser bead technology (41/11-plex Human Cytokine/Chemokine Arrays, Eve Technologies, Calgary, Canada). In line with previous documented ability of mast cells to produce pro-angiogenic factors [6, 7], IL-17A stimulated the secretion of fibroblast growth factor (FGF)-2 and vascular endothelial growth factor (VEGF) (Fig. 1q and r). Although the increases were relativiely small (2-fold increase for FGF-2 and 1.5-fold increase for VEGF), these observations demonstrate the potential role for mast cells in vascular remodeling in COPD. We used a relatively high concentration of IL-17A to activate mast cells. While the biological relevance of this concentration may be debated, the levels of IL-17A may be enriched in the pulmonary microenviroment. Furthermore, a ten fold lower dose was able to induce the secretion of FGF-2 in a pilot study (data not shown). Future studies investigating pulmonary mast cells isolated from COPD patients could provide imporant clues to the biological relevance of these initial findings.
The inflammatory mediator profile was, in contrast, unaffected by stimulation by IL-17A. The lack of pro-inflammatory responisveness of mast cells to IL-17A may be explained by earler reports of enhanced effects by other cytokines, such as TNFα, IL-1β and IL-22 . Thus, future studies investigating the potential inflammatory response of mast cells in response to IL-17A would benefit from including co-stimulation, or possibly the inflammatory milieu associated with COPD.
We next investigated the immunoreactivity for FGF-2 and VEGF in lung tissue specimens from end-stage COPD patients, to confirm expression by mast cells. In support of the in vitro data establishing a potential role for mast cells in the regulation of vascular growth factors in COPD, pulmonary mast cells were positive for both FGF-2 and VEGF (Fig. 1i and j). The biological relevance of this observation needs to be examined further, in particular as structural cells exhibit marked staining intensity in pulmonary tissue.
Both increased number of pulmonary vessels and vascular area is observed in COPD . Moreover, medial thickness of pulmonary vessels exhibit an inverse relation to lung function, suggesting increased vascular remodeling in advanced disease. Others have demonstrated that extra-pulmonary mast cells participate in vascular remodeling by the production of pro-angiogenic factors such as FGF-2 and VEGF [6, 7]. In addition, it was recently demonstrated that IL-17A directly induces the production of VEGF and FGF-2 by the endothelium .
The current data support increased IL-17 signaling in end-stage COPD, and stimulation of mast cell-derived vascular growth factors by IL-17A. Together, these findings designate a potential function for mast cells in advanced COPD, and warrant additional studies with the ultimate objective to target mast cells to reduce the morbidity associated with COPD.
The authors would like to thank Joanna Kasinska, Marie Bailey (McMaster University, Hamilton, Canada), Britt-Marie G Nilsson, Karin Jansner (Lund University, Lund, Sweden), Ellen Margrete Raaby and Beatriz Seville-Jensen (Aarhus University, Denmark) for excellent technical support.
Canadian Institutes of Health Research (MOP-64390 and MOP-87517), the Swedish Heart-lung Foundation, the Swedish Research Council, the Swedish Society for Medical Research. The funding sources had no influence on study design, sample collection, data analysis and interpretation, or preparation of this manuscript.
Availability of data and materials
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
Conception and design: ABR, MM, HKG, LB, AL, JSE, HJH and MRS. Acquisition of data: ABR, MM, HKG, LB. Analysis and interpretation: ABR, MM, HKG, AL, LB, JSE, HJH and MRS. Drafting the manuscript for important intellectual content: ABR, MM, HKG, LB, AL, JSE, HJH and MRS. All authors approved the final version to be published.
ABR is employed by AstraZeneca. There are no other competing interest with regard to this manuscript to declare.
Consent for publication
Ethics approval and consent to participate
Informed consent was obtained from all subjects within the study. The local research ethics board in Lund, Sweden approved the study protocol and written consent form.
Canadian Institutes of Health Research (MOP-64390 and MOP-87517), the Swedish Heart-lung Foundation, the Swedish Research Council, the Swedish Society for Medical Research.
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