Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stress

被引:32
作者
Evans, CAW
Harbuz, MS
Ostenfeld, T
Norrish, A
Blackwell, JM
机构
[1] Addenbrookes Hosp, Wellcome Trust Ctr Mol Mech Dis, Cambridge CB2 2XY, England
[2] Univ Bristol, Bristol Royal Infirm, URC Neuroendocrinol, Bristol BS2 8HW, Avon, England
[3] Univ Cambridge, MRC, Ctr Brain Repair, Cambridge CB2 2PY, England
基金
英国惠康基金;
关键词
divalent cation transporter; hypothalamus-pituitary-adrenal axis; toxoplasma; corticotrophin releasing hormone; corticosterone;
D O I
10.1007/s100480100105
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The gene Nramp1 encoding the natural resistance-associated macrophage protein (Nramp1) influences susceptibility to intracellular infections and autoimmune diseases, and the humoral response to stress. Nramp1 functions as a proton/divalent cation antiporter in the membranes of late endosomes/lysosomes, regulating cytoplasmic iron levels in macrophages. The Drosophila homologue of Nramp1 is expressed in sensory neurons and macrophages, and influences taste behaviour directly through divalent cation transport. Here we demonstrate that murine Nramp1 is also expressed on neurons as well as microglial cells in the brain and influences the behavioural response to stress, hypothalamuspituitary-adrenal (HPA) axis activation and mortality following Toxoplasma gondii infection in control and prestressed mice. We hypothesise that, although differences in HPA activation translate into differences in adrenal enlargement and basal circulating corticosterone levels, the primary influence of Nramp1 is at the level of the neuronal response to stress. These results provide new insight into the possible roles of divalent cation transporters of the Nramp gene family in regulating metal ion homeostasis in the brain and its pathological implications.
引用
收藏
页码:69 / 78
页数:10
相关论文
共 68 条
[1]   A factor with a zinc- and phorbol ester-binding domain is necessary for endosome fusion [J].
Aballay, A ;
Arenas, NG ;
Quest, AFG ;
Mayorga, LS .
EXPERIMENTAL CELL RESEARCH, 1997, 235 (01) :28-34
[2]   Zn2+ depletion blocks endosome fusion [J].
Aballay, A ;
Sarrouf, MN ;
Colombo, MI ;
Stahl, PD ;
Mayorga, LS .
BIOCHEMICAL JOURNAL, 1995, 312 :919-923
[3]  
Atkinson BL, 1997, J CELL BIOCHEM, V65, P325, DOI 10.1002/(SICI)1097-4644(19970601)65:3<325::AID-JCB3>3.3.CO
[4]  
2-G
[5]   Ectopic expression of Nramp1 in COS-1 cells modulates iron accumulation [J].
Atkinson, PGP ;
Barton, CH .
FEBS LETTERS, 1998, 425 (02) :239-242
[6]  
BANERJEE A, 1990, J BIOL CHEM, V265, P1794
[7]   A CORTICOTROPIN-RELEASING FACTOR ANTAGONIST REVERSES THE STRESS-INDUCED CHANGES OF EXPLORATORY-BEHAVIOR IN MICE [J].
BERRIDGE, CW ;
DUNN, AJ .
HORMONES AND BEHAVIOR, 1987, 21 (03) :393-401
[8]   CRF AND RESTRAINT-STRESS DECREASE EXPLORATORY-BEHAVIOR IN HYPOPHYSECTOMIZED MICE [J].
BERRIDGE, CW ;
DUNN, AJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1989, 34 (03) :517-519
[9]   Genetic regulation of macrophage activation:: understanding the function of Nramp1 (= Ity/Lsh/Bcg) [J].
Blackwell, JM ;
Searle, S .
IMMUNOLOGY LETTERS, 1999, 65 (1-2) :73-80
[10]   Structure and function of the natural-resistance-associated macrophage protein (Nramp1), a candidate protein for infectious and autoimmune disease susceptibility [J].
Blackwell, JM .
MOLECULAR MEDICINE TODAY, 1996, 2 (05) :205-211