HO1 mRNA and Protein do not Change in Parallel in Bronchial Biopsies of Patients After Long Term Exposure to Sulfur Mustard
Mohammad Reza Nourani1, Samaneh Yazdani1,4, Mehryar Habibi Roudkenar3, Majid Ebrahimi1, Raheleh Halabian3, Leila Mirbagheri1,5, Mostafa Ghanei1 and Abbas Ali Imani Fooladi21Chemical Injury Research Center (CIRC), Baqiyatallah Medical Sciences University, Tehran, Iran. 2Research Center of Molecular B...
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Veröffentlicht in: | Gene regulation and systems biology 2010-01, Vol.2010 (4), p.83-90 |
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Zusammenfassung: | Mohammad Reza Nourani1, Samaneh Yazdani1,4, Mehryar Habibi Roudkenar3, Majid Ebrahimi1, Raheleh Halabian3, Leila Mirbagheri1,5, Mostafa Ghanei1 and Abbas Ali Imani Fooladi21Chemical Injury Research Center (CIRC), Baqiyatallah Medical Sciences University, Tehran, Iran. 2Research Center of Molecular Biology, Baqiyatallah Medical Sciences University, Tehran, Iran. 3Research Center, Iranian Blood Transfusion Organization, Tehran, Iran. 4Biochemistry Department, Payam Noor University, Tehran, Iran. 5Science and Research Branch, Department of Biology, Azad University, Tehran, Iran. AbstractSulfur mustard (SM), is an alkylating agent and has been emerged as a chemical weapon in various battlefields. More recently, SM was employed in the Iraq conflict against Iranian military forces and civilians. Nowadays there are more than 40,000 people suffering from pulmonary lesions special chronic obstructive pulmonary disease (COPD) due to mustard gas in Iran. SM causes the endogenous production of reactive oxygen species (ROS). Heme oxygenases (HOs) are the rate-limiting enzyme for heme metabolism. Numerous studies have confirmed that HOs are concerned in diverse biological processes such as anti-oxidation.The present study was undertaken to consider the regulation of HO-1 and HO-2 n the human airway wall, and to suggest a probable role that HOs may play in cellular defense against oxidative stress due to SM. In this research ten unexposed SM individuals and twenty SM exposed patients were included. Evaluation of HO-1& HO -2 expressions in unexposed and SM exposed patients samples was performed by semiquantitative RT-PCR, real-time RT-PCR and Immunohistochemistry analysis. While unexposed SM samples expressed same levels of HOs, expression level of HO-1was upregulated about 3.58 ± 1.93 folds in SM exposed patients in comparison with unexposed ones, we could not find any difference in expression of HO-2 n two groups. In contrast, Immunohistochemistry results showed negative HO-1 protein expression in SM injured patients.Our results revealed that HO1 may plays an important role in cellular protection against oxidative stress due to mustard gas toxicity in airway wall of SM exposed patients at mRNA level, but translational modifications might cause decrease in the amount of HO1 protein. |
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ISSN: | 1177-6250 1177-6250 |
DOI: | 10.4137/GRSB.S5871 |