Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3

Occupational exposure to crystalline silica (CS) results in a persistent pulmonary inflammatory response that eventually leads to abnormal tissue repair, disability, and death. The inflammatory-immune responses occur in the early stages of CS exposure, and both innate and adaptive immunity are invol...

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Main Authors: Yiting Zhang, Chao Li, Siyi Li, Yiping Lu, Sitong Du, Xinning Zeng, Xi Chen, Jie Chen
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2019/3427053
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spelling doaj-433eb2af0fab46bd87970fafb5cf516a2020-11-24T21:52:48ZengHindawi LimitedMediators of Inflammation0962-93511466-18612019-01-01201910.1155/2019/34270533427053Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3Yiting Zhang0Chao Li1Siyi Li2Yiping Lu3Sitong Du4Xinning Zeng5Xi Chen6Jie Chen7Division of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaDivision of Pneumoconiosis, School of Public Health, China Medical University, Shenyang, ChinaOccupational exposure to crystalline silica (CS) results in a persistent pulmonary inflammatory response that eventually leads to abnormal tissue repair, disability, and death. The inflammatory-immune responses occur in the early stages of CS exposure, and both innate and adaptive immunity are involved. CD4+ T cells play a pivotal role in the pathogenesis of CS-induced pulmonary disease, which has no proven curative therapy. Dihydrotanshinone I (DHI), a natural product isolated from Salvia miltiorrhiza Bunge (Danshen), has anti-inflammatory and immunomodulatory properties. However, whether DHI has a protective effect on CS-induced lung disease, how it influences the Th immune response, and the potential underlying molecular mechanism(s) have not been fully clarified. In this study, DHI treatment of CS-exposed mice reduced the expression of proinflammatory cytokines and the infiltration of immune cells. It significantly ameliorated CS-induced pulmonary inflammation by attenuating T helper (Th)1 and Th17 responses, which were tightly related to the inhibition of STAT1 and STAT3. DHI significantly altered Th2 cytokines but not the Th2 nuclear transcription factor. Furthermore, our study found that DHI treatment also affected regulatory T cell activity in CS-injured mice. Taken together, our findings indicated that DHI could modulate Th responses and alleviate CS-induced pulmonary inflammation, suggesting a novel application of DHI in CS-induced pulmonary disease.http://dx.doi.org/10.1155/2019/3427053
collection DOAJ
language English
format Article
sources DOAJ
author Yiting Zhang
Chao Li
Siyi Li
Yiping Lu
Sitong Du
Xinning Zeng
Xi Chen
Jie Chen
spellingShingle Yiting Zhang
Chao Li
Siyi Li
Yiping Lu
Sitong Du
Xinning Zeng
Xi Chen
Jie Chen
Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3
Mediators of Inflammation
author_facet Yiting Zhang
Chao Li
Siyi Li
Yiping Lu
Sitong Du
Xinning Zeng
Xi Chen
Jie Chen
author_sort Yiting Zhang
title Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3
title_short Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3
title_full Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3
title_fullStr Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3
title_full_unstemmed Dihydrotanshinone I Alleviates Crystalline Silica-Induced Pulmonary Inflammation by Regulation of the Th Immune Response and Inhibition of STAT1/STAT3
title_sort dihydrotanshinone i alleviates crystalline silica-induced pulmonary inflammation by regulation of the th immune response and inhibition of stat1/stat3
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2019-01-01
description Occupational exposure to crystalline silica (CS) results in a persistent pulmonary inflammatory response that eventually leads to abnormal tissue repair, disability, and death. The inflammatory-immune responses occur in the early stages of CS exposure, and both innate and adaptive immunity are involved. CD4+ T cells play a pivotal role in the pathogenesis of CS-induced pulmonary disease, which has no proven curative therapy. Dihydrotanshinone I (DHI), a natural product isolated from Salvia miltiorrhiza Bunge (Danshen), has anti-inflammatory and immunomodulatory properties. However, whether DHI has a protective effect on CS-induced lung disease, how it influences the Th immune response, and the potential underlying molecular mechanism(s) have not been fully clarified. In this study, DHI treatment of CS-exposed mice reduced the expression of proinflammatory cytokines and the infiltration of immune cells. It significantly ameliorated CS-induced pulmonary inflammation by attenuating T helper (Th)1 and Th17 responses, which were tightly related to the inhibition of STAT1 and STAT3. DHI significantly altered Th2 cytokines but not the Th2 nuclear transcription factor. Furthermore, our study found that DHI treatment also affected regulatory T cell activity in CS-injured mice. Taken together, our findings indicated that DHI could modulate Th responses and alleviate CS-induced pulmonary inflammation, suggesting a novel application of DHI in CS-induced pulmonary disease.
url http://dx.doi.org/10.1155/2019/3427053
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