Citation

Pashandi Z, Saraygord-Afshari N, Naderi-Manesh H, Naderi M. Int. J. Proteomics 2015; 2015: 659241.

Affiliation

Department of Ophthalmology, Chemical Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Copyright

(Copyright © 2015, Hindawi Publishing)

DOI

10.1155/2015/659241

PMID

25685557

PMCID

PMC4320800

Abstract

OBJECTIVE. Sulfur mustard (SM) is a highly reactive alkylating agent which produces ocular, respiratory, and skin damages. Eyes are the most sensitive organ to SM due to high intrinsic metabolic and rapid turnover rate of corneal epithelium and aqueous-mucous interfaces of the cornea and conjunctiva. Here we investigate underlying molecular mechanism of SM exposure delayed effects which is still a controversial issue after about 30 years.

MATERIALS AND METHODS. Following ethical approval, we have analyzed serum proteome of ten severe SM exposed male patients with delayed eye symptoms with two-dimensional electrophoresis followed by matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry. The western blotting was used to confirm the proteins that have been identified.

RESULTS. We have identified thirteen proteins including albumin, haptoglobin, and keratin isoforms as well as immunoglobulin kappa chain which showed upregulation while transferrin and alpha 1 antitrypsin revealed downregulation in these patients in comparison with healthy control group.

CONCLUSIONS. Our results elevated participation of free iron circulatory imbalance and local matrix-metalloproteinase activity in development of delayed ocular symptoms induced by SM. It demonstrates that SM induced systemic toxicity leads to some serum protein changes that continually and gradually exacerbate the ocular surface injuries.

Language: en