Transport of maternal cholesterol to the fetus is affected by maternal plasma cholesterol concentrations in the Golden Syrian hamster

被引:56
作者
Burke, Katie T. [1 ]
Colvin, Perry L. [3 ,4 ]
Myatt, Leslie [2 ]
Graf, Gregory A. [5 ,6 ]
Schroeder, Friedhelm [7 ]
Woollett, Laura A. [1 ]
机构
[1] Univ Cincinnati, Sch Med, Dept Pathol & Lab Med, Cincinnati, OH 45237 USA
[2] Univ Cincinnati, Sch Med, Dept Obstet & Gynecol, Cincinnati, OH 45237 USA
[3] Univ Maryland, Sch Med, Dept Internal Med, Baltimore, MD 21201 USA
[4] Univ Maryland, Sch Med, Div Gerontol, Baltimore, MD 21201 USA
[5] Univ Kentucky, Dept Pharmaceut Sci, Lexington, KY 40536 USA
[6] Univ Kentucky, Cardiovasc Res Ctr, Lexington, KY 40536 USA
[7] Texas A&M Univ, Dept Physiol & Pharmacol, College Stn, TX 77843 USA
关键词
placenta; yolk sac; Smith-Lemli-Opitz Syndrome; low density lipoprotein; high density lipoprotein; liver X receptor; NPC1; Like; 1; LOW-DENSITY-LIPOPROTEIN; LEMLI-OPITZ-SYNDROME; YOLK-SAC; PLACENTAL-TRANSFER; REDUCTASE-ACTIVITY; STEROL-METABOLISM; RECEPTOR-ACTIVITY; APOLIPOPROTEIN-B; BIRTH-WEIGHT; IN-VIVO;
D O I
10.1194/jlr.M800538-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The fetus has a high requirement for cholesterol and synthesizes cholesterol at elevated rates. Recent studies suggest that fetal cholesterol also can be obtained from exogenous sources. The purpose of the current study was to examine the transport of maternal cholesterol to the fetus and determine the mechanism responsible for any cholesterol-driven changes in transport. Studies were completed in pregnant hamsters with normal and elevated plasma cholesterol concentrations. Cholesterol feeding resulted in a 3.1-fold increase in the amount of LDL-cholesterol taken up by the fetus and a 2.4-fold increase in the amount of HDL-cholesterol taken up. LDL-cholesterol was transported to the fetus primarily by the placenta, and HDL-cholesterol was transported by the yolk sac and placenta. Several proteins associated with sterol transport and efflux, including those induced by activated liver X receptor, were expressed in hamster and human placentas: NPC1, NPC1L1, ABCA2, SCP-x, and ABCG1, but not ABCG8. NPC1L1 was the only protein increased in hypercholesterolemic placentas. Thus, increasing maternal lipoprotein-cholesterol concentrations can enhance transport of maternal cholesterol to the fetus, leading to 1) increased movement of cholesterol down a concentration gradient in the placenta, 2) increased lipoprotein secretion from the yolk sac (shown previously), and possibly 3) increased placental NPC1L1 expression.-Burke, K. T., P. L. Colvin, L. Myatt, G. A. Graf, F. Schroeder, and L. A. Woollett. Transport of maternal cholesterol to the fetus is affected by maternal plasma cholesterol concentrations in the Golden Syrian hamster. J. Lipid Res. 2009. 50: 1146-1155.
引用
收藏
页码:1146 / 1155
页数:10
相关论文
共 87 条
[1]  
Atshaves BP, 1999, J LIPID RES, V40, P610
[2]   The developmental origins of adult disease [J].
Barker, DJP .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2004, 23 (06) :588S-595S
[3]  
BAUM CL, 1993, J LIPID RES, V34, P729
[4]   STEROL SYNTHESIS AND LOW-DENSITY LIPOPROTEIN CLEARANCE INVIVO IN THE PREGNANT RAT, PLACENTA, AND FETUS - SOURCES FOR TISSUE CHOLESTEROL DURING FETAL DEVELOPMENT [J].
BELKNAP, WM ;
DIETSCHY, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (06) :2077-2085
[5]   HMG-COA REDUCTASE-ACTIVITY IN THE MICROSOMAL FRACTION FROM HUMAN-PLACENTA IN EARLY AND TERM PREGNANCY [J].
BOGUSLAWSKI, W ;
SOKOLOWSKI, W .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1984, 16 (09) :1023-1026
[6]   Metabolic syndrome in childhood: Association with birth weight, maternal obesity, and gestational diabetes mellitus [J].
Boney, CM ;
Verma, A ;
Tucker, R ;
Vohr, BR .
PEDIATRICS, 2005, 115 (03) :E290-E296
[7]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[8]   Maternal anthropometric and metabolic factors in the first half of pregnancy and risk of neonatal macrosomia in term pregnancies. A prospective study [J].
Clausen, T ;
Burski, TK ;
Oyen, N ;
Godang, K ;
Bollerslev, J ;
Henriksen, T .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2005, 153 (06) :887-894
[9]   Teratogen-mediated inhibition of target tissue response to Shh signaling [J].
Cooper, MK ;
Porter, JA ;
Young, KE ;
Beachy, PA .
SCIENCE, 1998, 280 (5369) :1603-1607
[10]   A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis [J].
Cooper, MK ;
Wassif, CA ;
Krakowiak, PA ;
Taipale, J ;
Gong, RY ;
Kelley, RI ;
Porter, FD ;
Beachy, PA .
NATURE GENETICS, 2003, 33 (04) :508-513