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Sp-A and Tlr4 Localization in Lung Tissue of Sm-Exposed Patients Publisher Pubmed



Ghaffarpour S1 ; Foroutan A2 ; Askari N3 ; Abbas FM4 ; Salehi E5 ; Nikoonejad M1 ; Naghizadeh MM1, 6 ; Eskandarian M7 ; Moghadam KG8 ; Akbari HMH9, 12 ; Yarmohammadi ME10 ; Ghazanfari T1, 11
Authors
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Authors Affiliations
  1. 1. Immunoregulation Research Center, Shahed University, Tehran, Iran
  2. 2. Department of Physiology, Shaheed Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Department of Biology, Faculty of Basic Sciences, Shahid Bahonar, University of Kerman, Kerman, Iran
  4. 4. Department of Oral & Maxillofacial Pathology, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  5. 5. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Non Communicable Diseases Research Center, Fasa University of Medical Science, Fasa, Iran
  7. 7. Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  8. 8. Internal Medicine Department, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Department of Pathology, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  10. 10. Department of Otolaryngology, Shahed University, Tehran, Iran
  11. 11. Department of Immunology, Shahed University, Tehran, Iran
  12. 12. Traditional Medicine School, Tehran University of Medical Sciences, Tehran, Iran

Source: International Immunopharmacology Published:2020


Abstract

Introduction: Long-term pulmonary complications are one of the major long-term consequences of sulfur mustard (SM) exposure. Toll-like receptor 4 (TLR4) involves in the pathogenesis of several pulmonary disorders. Surfactant protein-A (SP-A) regulates LPS-induced TLR4 localization and activation responses. However, the intensity and significance of TLR4 and SP-A expression by lung cells in SM-exposed patients is not clear. Methods: The gene expression of TLR4 (through real-time PCR) and TLR4 and SP-A positive cells and alveolar type II cells, as SP-A producers, (using IHC) were assessed in formalin fixed paraffin embedded (FFPE) specimens from SM-exposed (n = 17), and non-SM exposed individuals (n = 12). Results: TLR4 gene expression did not change between study groups. However, its cell surface presentation was significantly reduced in SM-exposed patients and particularly in which with constrictive bronchiolitis compared with the control group (P < 0.001 and P = 0.002, respectively). Frequency of alveolar type II cells was lower in the case group rather than the control group while the number of SP-A positive cells did not alter. Conclusions: These findings suggest that reduced TLR4 cell surface presentation may have anti-inflammatory function and SP-A may have a critical role in regulation of inflammatory responses in SM-exposed patients. Further investigation on other possible mechanisms involved in TLR4 internalization maybe help to illustrate the modulatory or inflammatory activity of TLR4 in these patients. © 2019