GENERATION, CHARACTERIZATION, AND HISTOCHEMICAL APPLICATION OF MONOCLONAL-ANTIBODIES SELECTIVELY RECOGNIZING OXIDATIVELY MODIFIED APO-B-CONTAINING SERUM-LIPOPROTEINS

被引:76
作者
HAMMER, A
KAGER, G
DOHR, G
RABL, H
GHASSEMPUR, I
JURGENS, G
机构
[1] GRAZ UNIV, FAC MED, INST MED BIOCHEM, A-8010 GRAZ, AUSTRIA
[2] GRAZ UNIV, FAC MED, INST HISTOL & EMBRYOL, A-8010 GRAZ, AUSTRIA
[3] GRAZ UNIV, FAC MED, DEPT SURG, A-8010 GRAZ, AUSTRIA
关键词
MODIFIED LIPOPROTEINS; APO-B LIPID PEROXIDATION; MONOCLONAL ANTIBODIES; ATHEROSCLEROSIS;
D O I
10.1161/01.ATV.15.5.704
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To investigate either the role oxidized LDL plays in atherosclerosis or structural changes on the surface of oxidized LDL, monoclonal antibodies (mAbs) are an important tool. After immunizing mice with Cu2+-oxidized LDL (oxLDL) and fusion of splenocytes, hybridoma supernatants were screened and cloned. Two mAbs, OB/04 and OB/09 (IgG and IgM), were further characterized. In solid-phase fluorescence immunoassays and Western blot analysis both mAbs reacted with oxLDL, LDL oxidized by a free radical-generating azo compound, or oxVLDL but not with native LDL, acetylated LDL, oxHDL(3), azo-oxidized HDL(3), or HDL(3) modified with malondialdehyde (MDA). In competitive immunoassays with LDL modified by oxidized fatty acid-derived aldehydes, mAb OB/09 strongly reacted with MDA-LDL or MDA-VLDL and LDL modified with 4-hydroxyhexenal followed by 4-hydroxynonenal but not with 4-hydroxyoctenal or hepta-2,4-dienal. mAb OB/04 had a weak affinity for LDL after modification with these aldehydes except for MDA-LDL. LDL modified with arachidonic acid oxidation products (AAOPs) was also recognized by this mAb. However, albumin modified either by the aldehydes applied or by AAOPs did not react with either mAb. Thus, the data indicate that each of the mAbs recognizes a different epitope that is expressed only on apoB-containing lipoproteins upon oxidative modification. An immunostaining with mAb OB/04 was obtained in areas rich in macrophages and in connective tissue of a human atherosclerotic lesion.
引用
收藏
页码:704 / 713
页数:10
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