Localization of the pre-squalene segment of the isoprenoid biosynthetic pathway in mammalian peroxisomes

被引:63
作者
Kovacs, Werner J.
Tape, Khanichi N.
Shackelford, Janis E.
Duan, Xueying
Kasumov, Takhar
Kelleher, Joanne K.
Brunengraber, Henri
Krisans, Skaidrite K.
机构
[1] ETH Honggerberg, HPM, Inst Cell Biol, CH-8093 Zurich, Switzerland
[2] San Diego State Univ, Dept Biol, San Diego, CA 92182 USA
[3] Univ Giessen, Dept Anat & Cell Biol, Div Med Cell Biol, D-35385 Giessen, Germany
[4] Case Western Reserve Univ, Dept Nutr, Cleveland, OH 44106 USA
[5] MIT, Dept Biomed Engn, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
cholesterol biosynthesis; isoprenoid; peroxisomes; mass isotopomer distribution; HepG2;
D O I
10.1007/s00418-006-0254-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies have indicated that the early steps in the isoprenoid/cholesterol biosynthetic pathway occur in peroxisomes. However, the role of peroxisomes in cholesterol biosynthesis has recently been questioned in several reports concluding that three of the peroxisomal cholesterol biosynthetic enzymes, namely mevalonate kinase, phosphomevalonate kinase, and mevalonate diphosphate decarboxylase, do not localize to peroxisomes in human cells even though they contain consensus peroxisomal targeting signals. We re-investigated the subcellular localization of the cholesterol biosynthetic enzymes of the pre-squalene segment in human cells by using new stable isotopic techniques and data computations with isotopomer spectral analysis, in combination with immunofluorescence and cell permeabilization techniques. Our present findings clearly show and confirm previous studies that the pre-squalene segment of the cholesterol biosynthetic pathway is localized to peroxisomes. In addition, our data are consistent with the hypothesis that acetyl-CoA derived from peroxisomal beta-oxidation of very long-chain fatty acids and medium-chain dicarboxylic acids is preferentially channeled to cholesterol synthesis inside the peroxisomes without mixing with the cytosolic acetyl-CoA pool.
引用
收藏
页码:273 / 290
页数:18
相关论文
共 66 条
[1]   Characterization of peroxisomal 3-hydroxy-3-methylglutaryl coenzyme a reductase in UT2*cells: Sterol biosynthesis, phosphorylation, degradation, and statin inhibition [J].
Aboushadi, N ;
Shackelford, JE ;
Jessani, N ;
Gentile, A ;
Krisans, SK .
BIOCHEMISTRY, 2000, 39 (01) :237-247
[2]   CONTROLLED SYNTHESIS OF HBSAG IN A DIFFERENTIATED HUMAN-LIVER CARCINOMA-DERIVED CELL-LINE [J].
ADEN, DP ;
FOGEL, A ;
PLOTKIN, S ;
DAMJANOV, I ;
KNOWLES, BB .
NATURE, 1979, 282 (5739) :615-616
[3]   PARTIAL DISASSEMBLY OF PEROXISOMES [J].
ALEXSON, SEH ;
FUJIKI, Y ;
SHIO, H ;
LAZAROW, PB .
JOURNAL OF CELL BIOLOGY, 1985, 101 (01) :294-304
[4]  
Amery L, 2000, J LIPID RES, V41, P1752
[5]   Identification, purification and characterization of an acetoacetyl-CoA thiolase from rat liver peroxisomes [J].
Antonenkov, VD ;
Croes, K ;
Waelkens, E ;
Van Veldhoven, PP ;
Mannaerts, GP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (10) :2981-2990
[6]   The rat liver peroxisomal membrane forms a permeability barrier for cofactors but not for small metabolites in vitro [J].
Antonenkov, VD ;
Sormunen, RT ;
Hiltunen, JK .
JOURNAL OF CELL SCIENCE, 2004, 117 (23) :5633-5642
[7]   The behavior of peroxisomes in vitro: mammalian peroxisomes are osmotically sensitive particles [J].
Antonenkov, VD ;
Sormunen, RT ;
Hiltunen, JK .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (06) :C1623-C1635
[8]   In vitro modeling of fatty acid synthesis under conditions simulating the zonation of lipogenic [13C]acetyl-CoA enrichment in the liver [J].
Bederman, IR ;
Kasumov, T ;
Reszko, AE ;
David, F ;
Brunengraber, H ;
Kelleher, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (41) :43217-43226
[9]   Zonation of labeling of lipogenic acetyl-CoA across the liver - Implications for studies of lipogenesis by mass isotopomer analysis [J].
Bederman, IR ;
Reszko, AE ;
Kasumov, T ;
David, F ;
Wasserman, DH ;
Kelleher, JK ;
Brunengraber, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (41) :43207-43216
[10]  
BEIER K, 1988, EUR J CELL BIOL, V46, P383