Association of apolipoprotein E with α2-macroglobulin in human plasma
Apolipoprotein (apo) E plays a central role in the transport of lipids among different organs and cell types, whereas α2-macroglobulin (α2M) is responsible for the binding and inactivation of plasma proteases, as well as the transport of various cytokines, growth factors, and hormones. In the presen...
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doaj-94ae960f2c414a7c8dfef3f278d770502021-04-26T05:46:29ZengElsevierJournal of Lipid Research0022-22751998-12-01391223732386Association of apolipoprotein E with α2-macroglobulin in human plasmaLarbi Krimbou0Michel Tremblay1Jean Davignon2Jeffrey S. Cohn3Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, Quebec, Canada H2W 1R7Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, Quebec, Canada H2W 1R7Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, Quebec, Canada H2W 1R7To whom correspondence should be addressed.; Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, Quebec, Canada H2W 1R7Apolipoprotein (apo) E plays a central role in the transport of lipids among different organs and cell types, whereas α2-macroglobulin (α2M) is responsible for the binding and inactivation of plasma proteases, as well as the transport of various cytokines, growth factors, and hormones. In the present study, evidence is presented for direct binding of apoE with α2M in human plasma, based on the observation that two-dimensional non-denaturing gradient gel electrophoretic separation of plasma resulted in co-migration of apoE with α2M in a complex intermediate in size (18.5 nm in diameter) between low (LDL) and high density lipoproteins (HDL). ApoE associated with α2M could be immunoprecipitated from plasma with anti-human α2M antiserum. Purified apoE, labeled with 125I, bound to native and methylamine-activated α2M (α2M-MA) in vitro in a time- and concentration-dependent manner. ApoE bound to α2M-MA with greater affinity than α2M. The binding of apoE to both α2M and α2M-MA did not depend on the presence of lipid. Ingestion of an oral fat load resulted in a reduction in the amount of apoE associated with α2M. Sphingomyelin vesicles and very low density lipoproteins (VLDL), but not phosphatidylcholine vesicles or HDL3, inhibited the in vitro binding of 125I-labeled apoE3 to α2M and α2M-MA. Binding of 125I-labeled apoE3 was also partially inhibited by an excess of platelet-derived growth factor and β-amyloid protein, but not interferon-γ. Subjects with an apoE 4/4 phenotype had less apoE associated with α2M in plasma than subjects with an apoE 3/3 or 2/2 phenotype, corresponding to reduced in vitro binding of apoE4 with α2M or α2M-MA. Although the functional significance of apoE binding to α2M remains to be determined, the present results demonstrate that: 1) apoE is non-covalently bound to α2M in human plasma, 2) α2M-MA has a greater capacity to bind apoE than α2M, 3) various proteins or lipoproteins known to bind apoE or α2M can potentially affect the interaction of apoE with α2M, and 4) association of apoE with α2M or α2M-MA is dependent on apoE phenotype.—Krimbou, L., M. Tremblay, J. Davignon, and J. S. Cohn. Association of apolipoprotein E with α2-macroglobulin in human plasma. J. Lipid Res. 1998. 39: 2373–2386.http://www.sciencedirect.com/science/article/pii/S0022227520333162atherosclerosisAlzheimer's diseasehigh density lipoproteinLRP |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Larbi Krimbou Michel Tremblay Jean Davignon Jeffrey S. Cohn |
spellingShingle |
Larbi Krimbou Michel Tremblay Jean Davignon Jeffrey S. Cohn Association of apolipoprotein E with α2-macroglobulin in human plasma Journal of Lipid Research atherosclerosis Alzheimer's disease high density lipoprotein LRP |
author_facet |
Larbi Krimbou Michel Tremblay Jean Davignon Jeffrey S. Cohn |
author_sort |
Larbi Krimbou |
title |
Association of apolipoprotein E with α2-macroglobulin in human plasma |
title_short |
Association of apolipoprotein E with α2-macroglobulin in human plasma |
title_full |
Association of apolipoprotein E with α2-macroglobulin in human plasma |
title_fullStr |
Association of apolipoprotein E with α2-macroglobulin in human plasma |
title_full_unstemmed |
Association of apolipoprotein E with α2-macroglobulin in human plasma |
title_sort |
association of apolipoprotein e with α2-macroglobulin in human plasma |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
1998-12-01 |
description |
Apolipoprotein (apo) E plays a central role in the transport of lipids among different organs and cell types, whereas α2-macroglobulin (α2M) is responsible for the binding and inactivation of plasma proteases, as well as the transport of various cytokines, growth factors, and hormones. In the present study, evidence is presented for direct binding of apoE with α2M in human plasma, based on the observation that two-dimensional non-denaturing gradient gel electrophoretic separation of plasma resulted in co-migration of apoE with α2M in a complex intermediate in size (18.5 nm in diameter) between low (LDL) and high density lipoproteins (HDL). ApoE associated with α2M could be immunoprecipitated from plasma with anti-human α2M antiserum. Purified apoE, labeled with 125I, bound to native and methylamine-activated α2M (α2M-MA) in vitro in a time- and concentration-dependent manner. ApoE bound to α2M-MA with greater affinity than α2M. The binding of apoE to both α2M and α2M-MA did not depend on the presence of lipid. Ingestion of an oral fat load resulted in a reduction in the amount of apoE associated with α2M. Sphingomyelin vesicles and very low density lipoproteins (VLDL), but not phosphatidylcholine vesicles or HDL3, inhibited the in vitro binding of 125I-labeled apoE3 to α2M and α2M-MA. Binding of 125I-labeled apoE3 was also partially inhibited by an excess of platelet-derived growth factor and β-amyloid protein, but not interferon-γ. Subjects with an apoE 4/4 phenotype had less apoE associated with α2M in plasma than subjects with an apoE 3/3 or 2/2 phenotype, corresponding to reduced in vitro binding of apoE4 with α2M or α2M-MA. Although the functional significance of apoE binding to α2M remains to be determined, the present results demonstrate that: 1) apoE is non-covalently bound to α2M in human plasma, 2) α2M-MA has a greater capacity to bind apoE than α2M, 3) various proteins or lipoproteins known to bind apoE or α2M can potentially affect the interaction of apoE with α2M, and 4) association of apoE with α2M or α2M-MA is dependent on apoE phenotype.—Krimbou, L., M. Tremblay, J. Davignon, and J. S. Cohn. Association of apolipoprotein E with α2-macroglobulin in human plasma. J. Lipid Res. 1998. 39: 2373–2386. |
topic |
atherosclerosis Alzheimer's disease high density lipoprotein LRP |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520333162 |
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