Evidence of a role for both anti-Hsp70 antibody and endothelial surface membrane Hsp70 in atherosclerosis

• Published in: Cell stress & chaperones 2013-07, Vol.18 (4), p.483-493
• Main Authors: Leng, Xue, Wang, Xinxing, Pang, Wei, Zhan, Rui, Zhang, Zhiqing, Wang, Liqun, Gao, Xiujie, Qian, Lingjia
• Format: Article
• Language: English
• Subjects: Actins - immunology; Animals; Antibodies; Antibodies, Monoclonal - immunology; Atherosclerosis; Atherosclerosis - metabolism; Atherosclerosis - pathology; Autoantibodies; Autoantibodies - blood; Autoantibodies - immunology; Biochemistry; Biomedical and Life Sciences; Biomedicine; Blood plasma; Cancer Research; CD3 Complex - immunology; Cell Biology; Cell Membrane - metabolism; Cell membranes; Cells, Cultured; Disease Models, Animal; Endothelial cells; Endothelial Cells - cytology; Endothelial Cells - drug effects; Endothelial Cells - metabolism; Enzyme linked immunosorbent assay; Factor VIII - immunology; Heat shock proteins; HSP70 Heat-Shock Proteins - immunology; HSP70 Heat-Shock Proteins - metabolism; Immunology; Lipoproteins, LDL - toxicity; Neurons; Neurosciences; Original Paper; P branes; Rats; Rats, Sprague-Dawley
• ISSN: 1355-8145; 1466-1268
• DOI: 10.1007/s12192-013-0404-4

Although previous studies have shown that autoantigens such as Hsps have been implicated by induction of an autoimmune process in the development of atherosclerosis, the exact role of anti-Hsp70 antibody in atherosclerosis is unknown. In the present study, the levels of anti-Hsp70 autoantibodies and oxidized low density lipoprotein (OxLDL) were all significantly increased, and they were strongly correlated in an atherosclerosis model. After the endothelial cells were incubated with 20 μg/mL OxLDL for 12 h at 37 °C and followed by 90 min recovery, Hsp70 positive staining of OxLDL-treated endothelial cells was observed on the cell surface in immunostaining and flow cytometric analysis. This membrane Hsp70 was not from culture supernatant Hsp70 and binding of extracellular Hsp70 but was defined as endothelial surface membrane Hsp70. Furthermore, only in the OxLDL-treated group, but not in the untreated group, 51Cr-labeled endothelial cells were lysed by anti-Hsp70 antibody (BD091, IgAS) in the presence of either complement or peripheral blood mononuclear cells. Control antibodies, including IgNor, mAb to Hsp70 (SPA-810), and mAbs to Factor VIII, α-actin, and CD3 showed no cytotoxic effects. In conclusion, anti-Hsp70 antibodies could be reacting with the endothelial surface membrane Hsp70 induced by OxLDL and were able to mediate endothelial cytotoxicity. There is a possibility that a humoral immune reaction to endothelial surface membrane Hsp70 may play an important role in the pathogenesis of atherosclerosis.