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
[31]   Cloning and characterization of a mammalian proton-coupled metal-ion transporter [J].
Gunshin, H ;
Mackenzie, B ;
Berger, UV ;
Gunshin, Y ;
Romero, MF ;
Boron, WF ;
Nussberger, S ;
Gollan, JL ;
Hediger, MA .
NATURE, 1997, 388 (6641) :482-488
[32]   Host resistance to intracellular infection:: Mutation of natural resistance-associated macrophage protein 1 (Nramp1) impairs phagosomal acidification [J].
Hackam, DJ ;
Rotstein, OD ;
Zhang, WJ ;
Gruenheid, S ;
Gros, P ;
Grinstein, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (02) :351-364
[33]   RAPID CHANGES IN THE CONTENT OF PROENKEPHALIN-A AND CORTICOTROPIN RELEASING HORMONE MESSENGER-RNAS IN THE PARAVENTRICULAR NUCLEUS DURING MORPHINE-WITHDRAWAL IN URETHANE-ANESTHETIZED RATS [J].
HARBUZ, M ;
RUSSELL, JA ;
SUMNER, BEH ;
KAWATA, M ;
LIGHTMAN, SL .
MOLECULAR BRAIN RESEARCH, 1991, 9 (04) :285-291
[34]   CHANGES IN HYPOTHALAMIC CORTICOTROPIN-RELEASING FACTOR AND ANTERIOR-PITUITARY PROOPIOMELANOCORTIN MESSENGER-RNA DURING THE COURSE OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS [J].
HARBUZ, MS ;
LEONARD, JP ;
LIGHTMAN, SL ;
CUZNER, ML .
JOURNAL OF NEUROIMMUNOLOGY, 1993, 45 (1-2) :127-132
[35]   RESPONSES OF HYPOTHALAMIC AND PITUITARY MESSENGER-RNA TO PHYSICAL AND PSYCHOLOGICAL STRESS IN THE RAT [J].
HARBUZ, MS ;
LIGHTMAN, SL .
JOURNAL OF ENDOCRINOLOGY, 1989, 122 (03) :705-711
[36]   Evidence for altered control of hypothalamic CRF in immune-mediated diseases [J].
Harbuz, MS ;
Jessop, DS ;
Chowdrey, HS ;
Blackwell, JM ;
Larsen, PJ ;
Lightman, SL .
STRESS: BASIC MECHANISMS AND CLINICAL IMPLICATIONS, 1995, 771 :449-458
[37]  
Hirsch EC, 1998, MOVEMENT DISORD, V13, P39
[38]  
JELLINGER KA, 1993, ADV NEUROL, V60, P267
[39]   CRF ANTAGONIST PARTIALLY REVERSES CRF-INDUCED AND STRESS-INDUCED EFFECTS ON FEEDING [J].
KRAHN, DD ;
GOSNELL, BA ;
GRACE, M ;
LEVINE, AS .
BRAIN RESEARCH BULLETIN, 1986, 17 (03) :285-289
[40]  
Kuhn HG, 1997, J NEUROSCI, V17, P5820