Acquired immunogenicity of calf thymus DNA and LDL modified by b-ribose: A comparative study

被引:37
作者
Akhter, Firoz [1 ,2 ]
Khan, M. Salman [1 ]
Ahmad, Saheem [1 ]
机构
[1] Integral Univ, Dept Biosci, Lucknow 226026, Uttar Pradesh, India
[2] Integral Univ, Dept Bioengn, Lucknow 226026, Uttar Pradesh, India
关键词
Calf thymus DNA (CT-DNA); Lipoproteins; Immunogenicity; LOW-DENSITY-LIPOPROTEIN; GLYCATION END-PRODUCTS; IMMUNE-COMPLEXES; ADVANCED GLYCOSYLATION; ANTIBODIES; METHYLGLYOXAL; RECOGNITION; MECHANISM; DAMAGE;
D O I
10.1016/j.ijbiomac.2014.10.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glycation of biologically important macromolecules leads to the establishment of advanced glycation end products (AGEs) having significant role in the pathophysiology of various diseases. D-Ribose, is a highly reactive pentose sugar resulting in the rapid formation of AGEs. Formation of D-ribose derived glycated DNA and LDL has been previously demonstrated: however no comparative, extensive studies have been performed to assess the immunogenicity of D-ribose glycated calf thymus DNA (CT-DNA) and LDL. In the present study, the results showed that animals immunized with D-ribose modified CT-DNA and LDL induced antibodies as detected by direct binding and competition EL1SA. The modified CT-DNA and LEX were found to be highly immunogenic, eliciting high titer immunogen-specific antibodies, while the native forms of DNA was almost non-immunogenic. The induced antibodies from modified CT-DNA and LDL exhibited wide range of heterogeneity in recognizing various nucleic acid conformers. DNA bases and amino acids. Furthermore, Serum antibodies from diabetes and diabetes atherosclerosis patients were screened for their binding to native CT-DNA, LDL and glycated CT-DNA, LDL. Glycated CT-DNA showed almost equivalent binding to both diabetes and diabetic atherosclerosis group while high recognition was observed when glycated LDL was used as an antigen. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1222 / 1227
页数:6
相关论文
共 30 条
[1]  
Ahmad MI, 2011, INDIAN J BIOCHEM BIO, V48, P290
[2]   Glycoxidation of biological macromolecules: A critical approach to halt the menace of glycation [J].
Ahmad, Saheem ;
Khan, M. Salman ;
Akhter, Firoz ;
Khan, Mohd Sajid ;
Khan, Amir ;
Ashraf, J. M. ;
Pandey, Ramendra Pati ;
Shahab, Uzma .
GLYCOBIOLOGY, 2014, 24 (11) :979-990
[3]   Glycoxidative damage to human DNA: Neo-antigenic epitopes on DNA molecule could be a possible reason for autoimmune response in type 1 diabetes [J].
Ahmad, Saheem ;
Moinuddin ;
Shahab, Uzma ;
Habib, Safia ;
Khan, M. Salman ;
Alam, Khursheed ;
Ali, Asif .
GLYCOBIOLOGY, 2014, 24 (03) :281-291
[4]   Studies on glycation of human low density lipoprotein: A functional insight into physico-chemical analysis [J].
Ahmad, Saheem ;
Akhter, Firoz ;
Moinuddin ;
Shahab, Uzma ;
Khan, M. Salman .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2013, 62 :167-171
[5]   Inhibitory Effect of Metformin and Pyridoxamine in the Formation of Early, Intermediate and Advanced Glycation End-Products [J].
Ahmad, Saheem ;
Shahab, Uzma ;
Baig, Mohd. Hassan ;
Khan, Mohd. Sajid ;
Khan, M. Salman ;
Srivastava, A. K. ;
Saeed, Mohd ;
Moinuddin .
PLOS ONE, 2013, 8 (09)
[6]   Genotoxicity and immunogenicity of DNA-advanced glycation end products formed by methylglyoxal and lysine in presence of Cu2+ [J].
Ahmad, Saheem ;
Moinuddin ;
Dixit, Kiran ;
Shahab, Uzma ;
Alam, Khursheed ;
Ali, Asif .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 407 (03) :568-574
[7]   Bio-physical characterization of ribose induced glycation: A mechanistic study on DNA perturbations [J].
Akhter, Firoz ;
Khan, M. Salman ;
Shahab, Uzma ;
Moinuddin ;
Ahmad, Saheem .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2013, 58 :206-210
[8]   IDENTIFICATION OF THE MAJOR SITE OF APOLIPOPROTEIN-B MODIFICATION BY ADVANCED GLYCOSYLATION END-PRODUCTS BLOCKING UPTAKE BY THE LOW-DENSITY-LIPOPROTEIN RECEPTOR [J].
BUCALA, R ;
MITCHELL, R ;
ARNOLD, K ;
INNERARITY, T ;
VLASSARA, H ;
CERAMI, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (18) :10828-10832
[9]   MODIFICATION OF LOW-DENSITY-LIPOPROTEIN BY ADVANCED GLYCATION END-PRODUCTS CONTRIBUTES TO THE DYSLIPIDEMIA OF DIABETES AND RENAL-INSUFFICIENCY [J].
BUCALA, R ;
MAKITA, Z ;
VEGA, G ;
GRUNDY, S ;
KOSCHINSKY, T ;
CERAMI, A ;
VLASSARA, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9441-9445
[10]   LOW-DENSITY LIPOPROTEIN METABOLISM BY HUMAN MACROPHAGES ACTIVATED WITH LOW-DENSITY LIPOPROTEIN IMMUNE-COMPLEXES - A POSSIBLE MECHANISM OF FOAM CELL-FORMATION [J].
GRIFFITH, RL ;
VIRELLA, GT ;
STEVENSON, HC ;
LOPESVIRELLA, MF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :1041-1059