Role of vitamin D-binding protein in isocyanate-induced occupational asthma
The development of a serological marker for early diagnosis of isocyanate-induced occupational asthma (isocyanate-OA) may improve clinical outcome. Our previous proteomic study found that expression of vitamin D-binding protein (VDBP) was upregulated in the patients with isocyanate-OA. In the presen...
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Korean Society for Biochemistry and Molecular Biology
2012
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pubmed-33663252012-06-07 Role of vitamin D-binding protein in isocyanate-induced occupational asthma Kim, Sung-Ho Choi, Gil-Soon Nam, Young-Hee Kim, Joo-Hee Hur, Gyu-Young Kim, Seung-Hyun Park, Sang Myun Park, Hae-Sim Original Article The development of a serological marker for early diagnosis of isocyanate-induced occupational asthma (isocyanate-OA) may improve clinical outcome. Our previous proteomic study found that expression of vitamin D-binding protein (VDBP) was upregulated in the patients with isocyanate-OA. In the present study, we evaluated the clinical relevance of VDBP as a serological marker in screening for isocyanate-OA among exposed workers and its role in the pathogenesis of isocyanate-OA. Three study groups including 61 patients with isocyanate-OA (group I), 180 asymptomatic exposed controls (AECs, group II), 58 unexposed healthy controls (NCs, group III) were enrolled in this study. The baseline serum VDBP level was significantly higher in group I compared with groups II and III. The sensitivity and specificity for predicting the phenotype of isocyanate-OA with VDBP were 69% and 81%, respectively. The group I subjects with high VDBP (≥ 311 µg/ml) had significantly lower PC20 methacholine levels than did subjects with low VDBP. The in vitro studies showed that TDI suppressed the uptake of VDBP into RLE-6TN cells, which was mediated by the downregulation of megalin, an endocytic receptor of the 25-hydroxycholecalciferol-VDBP complex. Furthermore, toluene diisocyanate (TDI) increased VEGF production and secretion from this epithelial cells by suppression of 1,25-dihydroxycholecalciferol [1,25(OH)2D3] production. The findings of this study suggest that the serum VDBP level may be used as a serological marker for the detection of isocyanate-OA among workers exposed to isocyanate. The TDI-induced VEGF production/secretion was reversed by 1,25(OH)2D3 treatment, which may provide a potential therapeutic strategy for patients with isocyanate-OA. Korean Society for Biochemistry and Molecular Biology 2012-05-31 2012-02-08 /pmc/articles/PMC3366325/ /pubmed/22314196 http://dx.doi.org/10.3858/emm.2012.44.5.036 Text en Copyright © 2012 by the Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Kim, Sung-Ho Choi, Gil-Soon Nam, Young-Hee Kim, Joo-Hee Hur, Gyu-Young Kim, Seung-Hyun Park, Sang Myun Park, Hae-Sim |
spellingShingle |
Kim, Sung-Ho Choi, Gil-Soon Nam, Young-Hee Kim, Joo-Hee Hur, Gyu-Young Kim, Seung-Hyun Park, Sang Myun Park, Hae-Sim Role of vitamin D-binding protein in isocyanate-induced occupational asthma |
author_facet |
Kim, Sung-Ho Choi, Gil-Soon Nam, Young-Hee Kim, Joo-Hee Hur, Gyu-Young Kim, Seung-Hyun Park, Sang Myun Park, Hae-Sim |
author_sort |
Kim, Sung-Ho |
title |
Role of vitamin D-binding protein in isocyanate-induced occupational asthma |
title_short |
Role of vitamin D-binding protein in isocyanate-induced occupational asthma |
title_full |
Role of vitamin D-binding protein in isocyanate-induced occupational asthma |
title_fullStr |
Role of vitamin D-binding protein in isocyanate-induced occupational asthma |
title_full_unstemmed |
Role of vitamin D-binding protein in isocyanate-induced occupational asthma |
title_sort |
role of vitamin d-binding protein in isocyanate-induced occupational asthma |
description |
The development of a serological marker for early diagnosis of isocyanate-induced occupational asthma (isocyanate-OA) may improve clinical outcome. Our previous proteomic study found that expression of vitamin D-binding protein (VDBP) was upregulated in the patients with isocyanate-OA. In the present study, we evaluated the clinical relevance of VDBP as a serological marker in screening for isocyanate-OA among exposed workers and its role in the pathogenesis of isocyanate-OA. Three study groups including 61 patients with isocyanate-OA (group I), 180 asymptomatic exposed controls (AECs, group II), 58 unexposed healthy controls (NCs, group III) were enrolled in this study. The baseline serum VDBP level was significantly higher in group I compared with groups II and III. The sensitivity and specificity for predicting the phenotype of isocyanate-OA with VDBP were 69% and 81%, respectively. The group I subjects with high VDBP (≥ 311 µg/ml) had significantly lower PC20 methacholine levels than did subjects with low VDBP. The in vitro studies showed that TDI suppressed the uptake of VDBP into RLE-6TN cells, which was mediated by the downregulation of megalin, an endocytic receptor of the 25-hydroxycholecalciferol-VDBP complex. Furthermore, toluene diisocyanate (TDI) increased VEGF production and secretion from this epithelial cells by suppression of 1,25-dihydroxycholecalciferol [1,25(OH)2D3] production. The findings of this study suggest that the serum VDBP level may be used as a serological marker for the detection of isocyanate-OA among workers exposed to isocyanate. The TDI-induced VEGF production/secretion was reversed by 1,25(OH)2D3 treatment, which may provide a potential therapeutic strategy for patients with isocyanate-OA. |
publisher |
Korean Society for Biochemistry and Molecular Biology |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366325/ |
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1611534388474937344 |