|
|
||||||||
Correspondence to:
W. Gray Jerome, at current address: Department of Pathology, Vanderbilt University Medical Center, 1161 21st Ave South, Nashville, TN 37232-2561., jay.jerome{at}mcmail.vanderbilt.edu (E-mail)
In atherosclerotic lesions, macrophages store lipid in cytoplasmic inclusions and lysosomes. Regression studies show that lysosomal lipid is not as easily cleared as cytoplasmic inclusion lipid. Macrophages enriched with mildly oxidized low density lipoprotein (oxLDL) accumulate cholesteryl ester (CE) and free cholesterol (FC) in lysosomes. We examined whether lysosomal stores of cholesterol from oxLDL are cleared from THP-1 and mouse macrophages. As in previous studies, oxLDL-enriched THP-1 macrophages accumulated substantial lysosomal cholesterol. Surprisingly, less than 12% of oxLDL-derived lysosomal CE was cleared to efficient FC acceptors (e.g., cyclodextrins, apolipoprotein/phosphatidylcholine vesicles, and fetal bovine serum). Filipin staining showed that lysosomes of oxLDL-treated THP-1 cells contained FC, and despite removal of most of the cell FC (70;80%) by incubation with cyclodextrins, filipin staining of FC in lysosomes did not diminish. Also, when THP-1 macrophages were incubated with [3H]CE oxLDL, 73;76% of the [3H]CE was retained in a lysosomal hydrolysis resistant pool. In contrast, greater than 90% of acetylated low density lipoprotein (acLDL) [3H]CE was hydrolyzed. Furthermore, [3H]FC liberated from oxLDL [3H]CE was released at a slower rate to cyclodextrins than was [3H]FC from acLDL [3H]CE. In contrast, only 27% of oxLDL [3H]CE was resistant to hydrolysis in mouse macrophages, and the [3H]FC generated from oxLDL and acLDL [3H]CE was released to cyclodextrins at similar rates.
We conclude that lack of hydrolysis and efflux of oxLDL cholesterol is not exclusively inherent in oxLDL, but also requires specific cell factors present in one cell type but not the other.Yancey, P. G., and W. G. Jerome. Lysosomal cholesterol derived from mildly oxidized low density lipoprotein is resistant to efflux. J. Lipid Res. 2001. 42: 317;327.
Supplementary key words:
cholesterol-engorged lysosomes, cholesterol efflux, atherosclerosis
Copyright © 2001 by Lipid Research, Inc.
Original Article
Lysosomal cholesterol derived from mildly oxidized low density lipoprotein is resistant to efflux
Patricia G. Yanceya and
W. Gray Jeromea
a Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC 27157
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
P. G. Yancey, W. G. Jerome, H. Yu, E. E. Griffin, B. E. Cox, V. R. Babaev, S. Fazio, and M. F. Linton Severely altered cholesterol homeostasis in macrophages lacking apoE and SR-BI J. Lipid Res., May 1, 2007; 48(5): 1140 - 1149. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. E. Cox, E. E. Griffin, J. C. Ullery, and W. G. Jerome Effects of cellular cholesterol loading on macrophage foam cell lysosome acidification J. Lipid Res., May 1, 2007; 48(5): 1012 - 1021. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Delton-Vandenbroucke, J. Bouvier, A. Makino, N. Besson, J.-F. Pageaux, M. Lagarde, and T. Kobayashi Anti-bis(monoacylglycero)phosphate antibody accumulates acetylated LDL-derived cholesterol in cultured macrophages J. Lipid Res., March 1, 2007; 48(3): 543 - 552. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Bostrom, B. Magnusson, P.-A. Svensson, O. Wiklund, J. Boren, L. M. S. Carlsson, M. Stahlman, S.-O. Olofsson, and L. M. Hulten Hypoxia Converts Human Macrophages Into Triglyceride-Loaded Foam Cells Arterioscler. Thromb. Vasc. Biol., August 1, 2006; 26(8): 1871 - 1876. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. E. Griffin, J. C. Ullery, B. E. Cox, and W. G. Jerome Aggregated LDL and lipid dispersions induce lysosomal cholesteryl ester accumulation in macrophage foam cells J. Lipid Res., October 1, 2005; 46(10): 2052 - 2060. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. E. Dove, Y. R. Su, W. Zhang, W. G. Jerome, L. L. Swift, M. F. Linton, and S. Fazio ACAT1 Deficiency Disrupts Cholesterol Efflux and Alters Cellular Morphology in Macrophages Arterioscler. Thromb. Vasc. Biol., January 1, 2005; 25(1): 128 - 134. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Whatling, H. Bjork, S. Gredmark, A. Hamsten, and P. Eriksson Effect of macrophage differentiation and exposure to mildly oxidized LDL on the proteolytic repertoire of THP-1 monocytes J. Lipid Res., September 1, 2004; 45(9): 1768 - 1776. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Du, S. Schiavi, N. Wan, M. Levine, D. P. Witte, and G. A. Grabowski Reduction of Atherosclerotic Plaques by Lysosomal Acid Lipase Supplementation Arterioscler. Thromb. Vasc. Biol., January 1, 2004; 24(1): 147 - 154. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Journal of Biological Chemistry |
| Molecular and Cellular Proteomics | ASBMB Today |