Expression and p75 neurotrophin receptor dependence of cholesterol synthetic enzymes in adult mouse brain

被引:43
作者
Korade, Zeljka
Mi, Zhiping
Portugal, Carmel
Schor, Nina E.
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, Dept Pediat, Pediat Ctr Neurosci, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Neurol & Pharmacol, Pittsburgh, PA USA
关键词
p75 neurotrophin receptor; cholesterol; HMG-CoAred; 7dhcred; in situ hybridization;
D O I
10.1016/j.neurobiolaging.2006.06.026
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Normal brain function depends critically on cholesterol. Although cholesterol is synthesized locally in the adult brain, the precise anatomical localization of cholesterogenic enzymes is not known. Here we show that 3-hydroxy-3-inethylglutaryl-coenzyme A reductase (HMG-CoAred) and 7-dehydrocholesterol reductase (7dhcred), the first and last enzymes, respectively, in the cholesterol biosynthesis pathway, are co-expressed in neurons throughout adult murine brain. Co-localization is most prominent. in cortical, hippocampal, and cholinergic neurons. Since adult hippocampal and cholinoergic neurons express p75 neurotrophin receptors (p75NTR) we hypothesized that p75NTR regulates expression of cholesterogenic enzymes. Treatment of Neuro2a neuroblastoma cells or primary cerebellar cultures with siRNA downregulates p75NTR and decreases the expression level of HMG-CoAred and 7dhcred. Native nuroblastoma cell lines with differential expression of p75NTR differentially express 7dhcred; 7dhcred expression correlates with p75NTR expression. This suggests that, in p75NTR-expressing cells, p75NTR regulates cholesterol synthesis through regulation of HMG-CoAred and 7dhcred expression. The unexpected localization of cholesterogenic enzymes in adult neurons suggests that at least some adult neurons retain the ability to synthesize cholesterol. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1522 / 1531
页数:10
相关论文
共 48 条
[11]   SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver [J].
Horton, JD ;
Goldstein, JL ;
Brown, MS .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (09) :1125-1131
[12]   Combined analysis of oligonucleotide microarray data from transgenic and knockout mice identifies direct SREBP target genes [J].
Horton, JD ;
Shah, NA ;
Warrington, JA ;
Anderson, NN ;
Park, SW ;
Brown, MS ;
Goldstein, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12027-12032
[13]   Imaging lipid rafts [J].
Ishitsuka, R ;
Sato, SB ;
Kobayashi, T .
JOURNAL OF BIOCHEMISTRY, 2005, 137 (03) :249-254
[14]   Smith-Lemli-Opitz syndrome and the DHCR7 gene [J].
Jira, PE ;
Waterham, HR ;
Wanders, RJA ;
Smeitink, JAM ;
Sengers, RCA ;
Wevers, RA .
ANNALS OF HUMAN GENETICS, 2003, 67 :269-280
[15]  
JUREVICS H, 1995, J NEUROCHEM, V64, P895
[16]  
Koudinov AR, 2004, ACTA NEUROBIOL EXP, V64, P71, DOI 10.55782/ane-2004-1492
[17]   Central role of peroxisomes in isoprenoid biosynthesis [J].
Kovacs, WJ ;
Olivier, LM ;
Krisans, SK .
PROGRESS IN LIPID RESEARCH, 2002, 41 (05) :369-391
[18]   Purification of brain peroxisomes and localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase [J].
Kovacs, WJ ;
Faust, PL ;
Keller, GA ;
Krisans, SK .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (18) :4850-4859
[19]  
Kurrasch DM, 2004, METHOD ENZYMOL, V389, P3
[20]   CLEAVAGE OF POLY(ADP-RIBOSE) POLYMERASE BY A PROTEINASE WITH PROPERTIES LIKE ICE [J].
LAZEBNIK, YA ;
KAUFMANN, SH ;
DESNOYERS, S ;
POIRIER, GG ;
EARNSHAW, WC .
NATURE, 1994, 371 (6495) :346-347