Secretion of sterols and the NPC2 protein from primary astrocytes

被引:39
作者
Mutka, AL
Lusa, S
Linder, MD
Jokitalo, E
Kopra, O
Jauhiainen, M
Ikonen, E
机构
[1] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[2] Biomedicum Helsinki, Natl Publ Hlth Inst, Helsinki 00251, Finland
关键词
D O I
10.1074/jbc.M405345200
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
Astrocytes secrete cholesterol in lipoprotein particles. Here we show that primary murine embryonic astrocytes secrete endogenously synthesized cholesterol but also the cholesterol precursors desmosterol and lathosterol. In astrocyte membranes, desmosterol and cholesterol were the predominant sterols. Astrocytes derived from Niemann-Pick type C lipidosis (NPC1(-/-)) mice displayed late endosomal cholesterol deposits, but the secretion of biosynthetic sterols from the cells was not inhibited. Both wild-type and NPC1(-/-) astrocytes secreted the NPC2 protein. Size-exclusion chromatography combined with electron microscopy showed that the majority of sterols were secreted separately from NPC2 in heterogeneous spherical particles with an average diameter of 20 nm. These data suggest that NPC2 and the majority of sterols secreted from astrocytes are not released together and that the secretion of neither sterols nor NPC2 requires NPC1 function. In addition, the findings reveal a complexity of sterol species in astrocytes and bring up the possibility that some of the effects assigned to astrocyte cholesterol may be attributed to its penultimate precursors.
引用
收藏
页码:48654 / 48662
页数:9
相关论文
共 45 条
[1]   Sialin expression in the CNS implicates extralysosomal function in neurons [J].
Aula, N ;
Kopra, O ;
Jalanko, A ;
Peltonen, L .
NEUROBIOLOGY OF DISEASE, 2004, 15 (02) :251-261
[2]   Defective endocytic trafficking of NPC1 and NPC2 underlying infantile Niemann-Pick type C disease [J].
Blom, TS ;
Linder, MD ;
Snow, K ;
Pihko, H ;
Hess, MW ;
Jokitalo, E ;
Veckman, V ;
Syvänen, AC ;
Ikonen, E .
HUMAN MOLECULAR GENETICS, 2003, 12 (03) :257-272
[3]   Cholesterol addition to ER membranes alters conformation of SCAP, the SREBP escort protein that regulates cholesterol metabolism [J].
Brown, AJ ;
Sun, LP ;
Feramisco, JD ;
Brown, MS ;
Goldstein, JL .
MOLECULAR CELL, 2002, 10 (02) :237-245
[4]  
Connor WE, 1998, J LIPID RES, V39, P1404
[5]   Brain lipoprotein metabolism and its relation to neurodegenerative disease [J].
Danik, M ;
Champagne, D ;
Petit-Turcotte, C ;
Beffert, U ;
Poirier, J .
CRITICAL REVIEWS IN NEUROBIOLOGY, 1999, 13 (04) :357-407
[6]   Cholesterol metabolism in the brain [J].
Dietschy, JM ;
Turley, SD .
CURRENT OPINION IN LIPIDOLOGY, 2001, 12 (02) :105-112
[7]   Unique lipoproteins secreted by primary astrocytes from wild type, apoE (-/-), and human apoE transgenic mice [J].
Fagan, AM ;
Holtzman, DM ;
Munson, G ;
Mathur, T ;
Schneider, D ;
Chang, LK ;
Getz, GS ;
Reardon, CA ;
Lukens, J ;
Shah, JA ;
LaDu, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) :30001-30007
[8]   Structure of a cholesterol-binding protein deficient in Niemann-Pick type C2 disease [J].
Friedland, N ;
Liou, HL ;
Lobel, P ;
Stock, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (05) :2512-2517
[9]   Neurodegeneration in the Niemann-Pick C mouse: Glial involvement [J].
German, DC ;
Liang, CL ;
Song, T ;
Yazdani, U ;
Xie, C ;
Dietschy, JM .
NEUROSCIENCE, 2002, 109 (03) :437-450
[10]  
GOLDSTEIN JL, 1983, METHOD ENZYMOL, V98, P241