Expression of scavenger receptor class B type 1 (SR-BI) promotes microvillar channel formation and selective cholesteryl ester transport in a heterologous reconstituted system

被引:56
作者
Reaven, E [1 ]
Leers-Sucheta, S [1 ]
Nomoto, A [1 ]
Azhar, S [1 ]
机构
[1] Dept Vet Affairs, Palo Alto Hlth Care Syst, Ctr Geriatr Res Educ & Clin, Palo Alto, CA 94304 USA
关键词
D O I
10.1073/pnas.98.4.1613
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the "selective" cholesteryl ester (CE) uptake process, surface-associated lipoproteins [high density lipoprotein (HDL) and low density lipoprotein] are trapped in the space formed between closely apposed surface microvilli (microvillar channels) in hormone-stimulated steroidogenic cells. This is the same location where an HDL receptor (SR-BI) is found. In the current study, we sought to understand the relationship between SR-Bi and selective CE uptake in a heterologous insect cell system. Sf9 (Spodoptera frugiperda) cells overexpressing recombinant SR-BI were examined for (i) SR-BI protein by Western blot analysis and light or electron immunomicroscopy, and (ii) selective lipoprotein CE uptake by the use of radiolabeled or fluorescent (BODIPY-CE)-labeled HDL. Noninfected or infected control Sf9 cells do not express SR-BI, show microvillar channels, or internalize CEs, An unexpected finding was the induction of a complex channel system in Sf9 cells expressing SR-BI, SR-B1-expressing cells showed many cell surface double-membraned channels, immunogold SR-BI, apolipoprotein (HDL) labeling of the channels, and high levels of selective HDL-CE uptake. Thus, double-membraned channels can be induced by expression of recombinant SR-BI in a heterologous system, and these specialized structures facilitate both the binding of HDL and selective HDL-CE uptake.
引用
收藏
页码:1613 / 1618
页数:6
相关论文
共 31 条
  • [1] Identification of scavenger receptor SR-BI as a high density lipoprotein receptor
    Acton, S
    Rigotti, A
    Landschulz, KT
    Xu, SZ
    Hobbs, HH
    Krieger, M
    [J]. SCIENCE, 1996, 271 (5248) : 518 - 520
  • [2] Azhar S, 1998, J LIPID RES, V39, P1616
  • [3] AZHAR S, 1989, J LIPID RES, V30, P1799
  • [4] Azhar S, 1999, J CELL PHYSIOL, V180, P190, DOI 10.1002/(SICI)1097-4652(199908)180:2<190::AID-JCP7>3.3.CO
  • [5] 2-Q
  • [6] AZHAR S, 1988, J LIPID RES, V29, P869
  • [7] UPTAKE AND UTILIZATION OF LIPOPROTEIN CHOLESTERYL ESTERS BY RAT GRANULOSA-CELLS
    AZHAR, S
    TSAI, L
    REAVEN, E
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1047 (02) : 148 - 160
  • [8] BREWER HB, 1986, METHOD ENZYMOL, V128, P223
  • [9] de la Llera-Moya M, 1999, J LIPID RES, V40, P575
  • [10] DISSOCIATION OF TISSUE UPTAKE OF CHOLESTEROL ESTER FROM THAT OF APOPROTEIN-A-I OF RAT PLASMA HIGH-DENSITY LIPOPROTEIN - SELECTIVE DELIVERY OF CHOLESTEROL ESTER TO LIVER, ADRENAL, AND GONAD
    GLASS, C
    PITTMAN, RC
    WEINSTEIN, DB
    STEINBERG, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (17): : 5435 - 5439