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
[31]   Identification of HE1 as the second gene of Niemann-Pick C disease [J].
Naureckiene, S ;
Sleat, DE ;
Lackland, H ;
Fensom, A ;
Vanier, MT ;
Wattiaux, R ;
Jadot, M ;
Lobel, P .
SCIENCE, 2000, 290 (5500) :2298-+
[32]   A porcine homolog of the major secretory protein of human epididymis, HE1, specifically binds cholesterol [J].
Okamura, N ;
Kiuchi, S ;
Tamba, M ;
Kashima, T ;
Hiramoto, S ;
Baba, T ;
Dacheux, F ;
Dacheux, JL ;
Sugita, Y ;
Jin, YZ .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1999, 1438 (03) :377-387
[33]   EXPRESSION OF HETEROLOGOUS PROTEINS IN CULTURED RAT HIPPOCAMPAL-NEURONS USING THE SEMLIKI FOREST VIRUS VECTOR [J].
OLKKONEN, VM ;
LILJESTROM, P ;
GAROFF, H ;
SIMONS, K ;
DOTTI, CG .
JOURNAL OF NEUROSCIENCE RESEARCH, 1993, 35 (04) :445-451
[34]   Localization of Niemann-Pick C1 protein in astrocytes: Implications for neuronal degeneration in Niemann-Pick type C disease [J].
Patel, SC ;
Suresh, S ;
Kumar, U ;
Hu, CY ;
Cooney, A ;
Blanchette-Mackie, EJ ;
Neufeld, EB ;
Patel, RC ;
Brady, RO ;
Patel, YC ;
Pentchev, PG ;
Ong, WY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1657-1662
[35]   A riddle wrapped in a mystery: Understanding Niemann-Pick disease, type C [J].
Patterson, MC .
NEUROLOGIST, 2003, 9 (06) :301-310
[36]   Role of cholesterol in synapse formation and function [J].
Pfrieger, FW .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1610 (02) :271-280
[37]   A novel cholesterol stain reveals early neuronal cholesterol accumulation in the Niemann-Pick type C1 mouse brain [J].
Reid, PC ;
Sakashita, N ;
Sugii, S ;
Ohno-Iwashita, Y ;
Shimada, Y ;
Hickey, WF ;
Chang, TY .
JOURNAL OF LIPID RESEARCH, 2004, 45 (03) :582-591
[38]   Trafficking defects in endogenously synthesized cholesterol in fibroblasts, macrophages, hepatocytes, and glial cells from Niemann-Pick type C1 mice [J].
Reid, PC ;
Sugii, S ;
Chang, TY .
JOURNAL OF LIPID RESEARCH, 2003, 44 (05) :1010-1019
[39]   GROWTH AND LIPID-COMPOSITION OF RAT-BRAIN GLIAL-CELLS CULTURED IN LIPOPROTEIN DEFICIENT SERUM [J].
SHAH, SN ;
JOHNSON, RC .
NEUROCHEMICAL RESEARCH, 1986, 11 (06) :813-824
[40]   Genetic evidence for nonredundant functional cooperativity between NPC1 and NPC2 in lipid transport [J].
Sleat, DE ;
Wiseman, JA ;
El-Banna, M ;
Price, SM ;
Verot, L ;
Shen, MM ;
Tint, GS ;
Vanier, MT ;
Walkley, SU ;
Lobel, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (16) :5886-5891