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INSERM-UPMC U732, Hôpital Saint-Antoine, 184 rue du Faubourg Saint-Antoine, 75571 Paris Cedex 12, France

(Requests for offprints should be addressed to S M Parsadaniantz; Email: parsadan{at}st-antoine.inserm.fr)

G Banisadr is now at Department of Molecular Pharmacology and Biological Chemistry, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA

	Abstract

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
Chemokines are small secreted proteins that chemoattract and activate immune and non-immune cells both in vivo and in vitro. In addition to their well-established role in the immune system, several recent reports have suggested that chemokines and their receptors may also play a role in the central nervous system (CNS). The best known central action is their ability to act as immunoinflammatory mediators. Indeed, these proteins regulate leukocyte infiltration in the brain during inflammatory and infectious diseases. However, we and others recently demonstrated that they are expressed not only in neuroinflammatory conditions, but also constitutively by different cell types including neurons in the normal brain, suggesting that they may act as modulators of neuronal functions. The goal of this review is to highlight the role of chemokines in the control of neuroendocrine functions. First, we will focus on the expression of chemokines and their receptors in the CNS, with the main spotlight on the neuronal expression in the hypothalamo–pituitary system. Secondly, we will discuss the role – we can now suspect – of chemokines and their receptors in the regulation of neuroendocrine functions. In conclusion, we propose that chemokines can be added to the well-described neuroendocrine regulatory mechanisms, providing an additional fine modulatory tuning system in physiological conditions.

	Background

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
The history of chemokines started in 1977, when the secreted platelet factor 4 (PF4/CXCL4) was purified without any knowledge of its function (Walz et al. 1977, Wu et al. 1977). Two decades ago, the discovery that interleukin-8 (IL-8/CXCL8) showed chemotactic activity for neutrophils established that chemokines are key elements in the control of leukocyte migration (Yoshimura et al. 1987). A second major development in chemokine research occurred during 1995–1996, with the discovery that certain chemokines function as HIV-suppressive factors in vitro by blocking viral interaction with specific chemokine receptors and that some chemokine receptors act as co-receptors for viral entry (Cocchi et al. 1995, Bleul et al. 1996, Feng et al. 1996, Oberlin et al. 1996). It has become apparent over the past years that chemokines are involved in virtually all pathologies that present an inflammatory component. This includes nervous system pathologies, such as neurodegenerative or neuroinflammatory diseases, that induce the expression of a number of chemokines and chemokine receptors in activated astrocytes and microglia, suggesting their involvement in the activation of the central nervous system defense mechanisms (Bleul et al. 1996, Oberlin et al. 1996, Thibeault et al. 2001). However, we and others have demonstrated that some chemokines and their receptors are constitutively expressed by neuronal cells in normal adult brain and may function as neuromodulators. Among the described neuromodulatory activities of chemokines, the current literature postulates that chemokines could directly interact with neuroendocrine functions. It is this latter new concept that we would like to illustrate by reviewing recent results.

	Chemokine and chemokine receptor classification

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
Chemokines are a family of large peptides (60–100 amino acids (aa)). They are subdivided into four families based on the number and spacing of the conserved cysteine residues in the N-terminal position and are named CXC, CC, CX3C, and C, in agreement with the systematic nomenclature. All chemokines signal through G protein-coupled receptors (GPCR). In general, several chemokines can bind to the same receptor and, conversely, a given chemokine may recognize more than one receptor. However, there are exceptions where unique ligand–receptor pairs exist. To date, more than 50 chemokines and about 20 chemokine receptors have been identified. Their classification and nomenclature can be found in reviews (Murphy 2002, Floridi et al. 2003).

	Structure of chemokines

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
The structure of chemokines comprises three distinct domains: a highly flexible N-terminal domain, which is tamped down by the N-terminal cysteine(s), a long loop, which leads into three antiparallel ß-pleated sheets, and an -helix that overlies the sheets (Baggiolini & Loetscher 2000). The structural activities revealed that the N-terminal region is important for receptor binding and activation (Clark-Lewis et al. 1991, Proudfoot et al. 1996). Interestingly, all chemokine structures described to date more or less conform to this three-dimensional pattern, even though they may bear little homology in their primary amino acid sequence (Clark-Lewis et al. 1995, Clore & Gronenborn 1995).

	Chemokine–receptor interaction

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
Based largely on a well-known model, it was postulated that the N terminus and the extracellular loop of the chemokine receptor are responsible for the initial binding event. This interaction induces a conformational change allowing the N-terminal region of the ligand to interact with the helices of the receptor triggering signal transduction. However, as for many GPCRs, this two-site paradigm does not appear to hold true for all chemokine–receptor pairs. Additionally, it was reported that following chemokine interaction, several chemokine receptors undergo a dimerization (heterodimerization and homodimerization) and oligomerization process with membrane receptors for classical neurotransmitters, representing all critical steps in triggering biological responses (Vila-Coro et al. 1999, 2000, Mellado et al. 2001).

	Chemokine receptor-mediated signal transduction

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
Relating to second messenger systems modulated by chemokine receptors, one of the first pathways identified was the inhibition of adenylyl cyclase activity to reduce the intracellular cAMP levels, involving G i subunit of G proteins (Zheng et al. 1999, Bajetto et al. 2001). It was also established that the majority of chemokine receptors activate phospholipase C, involving Gq proteins. The latter leads to the formation of diacylglycerol and inositol 1,4,5-triphosphate with a subsequent increase in protein kinase C activity and transient elevations of cytosolic Ca²⁺ levels (Jones et al. 1995, Knall et al. 1996, Wells et al. 1998). More distal signaling pathways modulated by chemokines include the activation of the mitogen-activated protein kinase (PK) cascade, especially the pathway involving extra-cellular signal-regulated kinase 1/2 activation, as well as the phosphorylation of the cytoskeletal-associated kinases (Ganju et al. 1998a,b, Wang et al. 2000, Bajetto et al. 2001). Studies of chemokine receptor activation have also reported the activation of a family of proteins known as Janus kinases and signal transducers and activators of transcriptions (Mellado et al. 1998, Wong & Fish 1998, Vila-Coro et al. 1999). Chemokine receptors also activate the signaling pathway of nuclear factor- B.

	Involvement of chemokines in neuroendocrine interactions

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
Some chemokines such as cytokine-induced neutrophil chemoattractant (CINC), stromal cell-derived factor (SDF-1/CXCL12), and monocyte chemoattractant protein-1 (MCP-1/CCL2) have been found to be expressed in the hypothalamus (Banisadr et al. 2005a). Such neuroanatomical localization suggests possible neuroendocrine functions (Table 1).

The implication of chemokines in stress responses was reported in several studies. Initially, it was observed that IL-8/CXCL8 mRNA is expressed in the rat paraventricular nucleus (PVN), where corticotropin-releasing hormone is synthesized, and in the hippocampus, where negative feedback to hypothalamo–pituitary–adrenal axis is generated. Thus, IL-8/CXCL8 could be a component of a stress-related neuroendocrine system (Licinio et al. 1992). Moreover, after a noxious stimulation consecutive to a s.c. injection of bacterial lipopolysaccharides (LPS), an up-regulation of CINC and interferon -inducible protein (IP-10/CXCL10) mRNAs expression was found in the PVN (Sakamoto et al. 1996a, Reyes et al. 2003). In addition, it was observed that IP-10/CXCL10 expression is also up-regulated following LPS in the circumventricular organs (CVO) including the subfornical organ (SFO) and the area postrema. Other chemokines such as MCP-1/CCL2 and growth-related gene alpha (GRO /CXCL1) demonstrate a LPS responsiveness. Indeed, an up-regulation of MCP-1/CCL2 transcription is detected in the choroid plexus, CVO, blood vessels, and meninges (Thibeault et al. 2001, Reyes et al. 2003). GRO /CXCL1 also exhibits an up-regulation of its transcription in the PVN and the choroid plexus but not in the CVO (Reyes et al. 2003).

Immobilization stress can be liable for an overexpression of chemokine expression. Indeed, it was shown that CINC mRNA expression is increased during stress immobilization in the parvocellular and magnocellular subdivisions of the PVN but not in the supraoptic nucleus (SON). Moreover, CINC immunostaining intensity is increased in the posterior pituitary parallel to an increase in serum in response to stress immobilization, suggesting that CINC, synthesized in the PVN, could be axonally transported through the median eminence and released into the peripheral blood from the hypothalamo–neurohypophysial system (Sakamoto et al. 1996b).

Finally, painful stress induced by a noxious stimulation consecutively with s.c. injection of formalin into hind footpad increases the CINC immunoreactivity in the posterior pituitary and external layers of the median eminence and the CINC secretion in the peripheral blood (Matsumoto et al. 1997).

Chemokines and body temperature

Several studies demonstrated that chemokines are implicated in the pyrogenic responses. Indeed, injections of IL-8/CXCL8, macrophage inflammatory protein-1 alpha and beta (MIP-1 /CCL3 and MIP-1ß /CCL4), and RANTES/CCL5 induce hyperthermia. It was observed that MIP-1 /CCL3 and MIP-1ß /CCL4 administered intravenously in the rabbit or into the anterior hypothalamic/preoptic area (AH/POA), a region containing thermosensitive neurons in the rat, evoke a dose-dependent febrile response characteristic of endogenous pyrogen (Davatelis et al. 1989, Minano et al. 1990, 1991a). It was reported that these two chemokines present differences in their ability to induce hyperthermia. MIP-1ß /CCL4 causes an immediate and sustained rise in the body temperature of the rat, whereas MIP-1 /CCL3 exerts a hyperthermic response with a longer latency and lower magnitude (Myers et al. 1993, Minano et al. 1996). Moreover, it was observed that the co-injection of MIP-1 /CCL3 and MIP-1ß /CCL4 into the AH/POA attenuates the increase in body temperature by either chemokine injected alone (Minano et al. 1996). Effects of MIP-1 /CCL3 and MIP-1ß /CCL4 on the body temperature seem to be independent of the prostaglandin pathway, since the MIP-1-produced fever is not blocked by inhibitors of prostaglandin synthesis (Davatelis et al. 1989, Minano et al. 1991b). Another chemokine, RANTES/CCL5, is also a powerful hyperthermia molecule when injected directly into the AH/POA. Indeed, the action of RANTES/CCL5 is characterized by an immediate and an intense dose-related fever following injection. This effect is prevented by pretreatment with a prostaglandin synthesis inhibitor (Tavares & Minano 2000). The magnitude of the febrile response induced by RANTES/CCL5 is greater than that produced with equipotent dose of MIP-1ß /CCL4. It appears that the two chemokines RANTES/CCL5 and MIP-1ß /CCL4 present different pathway mechanisms to induce hyperthermia, although they share the same receptor CCR5. Indeed, it was established that microinjections of either MIP-1ß /CCL4 or RANTES/CCL5 into the AH/POA produce an immediate and intense fever, but pretreatment with a specific antibody against receptor CCR5 fails to affect the fever induced by MIP-1ß /CCL4, but significantly attenuates the febrile response induced by RANTES/CCL5. Therefore, it can be concluded that the receptor CCR5 is functionally involved in the modulation of body temperature by RANTES/CCL5, but not in the MIP-1ß /CCL4-induced fever mechanism (Tavares & Minano 2004).

Chemokines and feeding

It was discovered that chemokines can also alter food intake when centrally administered. Indeed, i.c.v. administration of PF4/CXCL4, a mediator of inflammatory and allergic responses, suppresses the 2-h nighttime and total daily food intake, whereas daytime food intake does not change. This effect of PF4/CXCL4 is centrally mediated, since an i.p. administration of PF4/CXCL4 has no effect on food intake (Plata-Salaman 1988). MIP-1 /CCL3 and MIP-1ß /CCL4 are also involved in the control of food intake. Indeed, when they are directly injected in the rat ventromedial hypothalamus (a structure implicated in the inhibition of feeding behavior) or into the rat AH/POA, they decrease feeding (Minano & Myers 1991, Myers et al. 1993). Moreover, it was reported in the rat that i.c.v. administration of two members of CXC chemokines, IL-8/CXCL8 and IP-10/CXCL10, and two members of CC chemokines, MCP-1/CCL2 and RANTES/CCL5, are also effective in decreasing the short-term (2 h) food intake (Plata-Salaman & Borkoski 1994). More recently, we demonstrated by immunohistochemical studies that SDF-1 /CXCL12 is constitutively expressed in melanin-concentrating hormone (MCH)-expressing neurons located in the lateral hypothalamic area (LHA), neurons which are mainly involved in the stimulation of food intake (Banisadr et al. 2003). Moreover, it was shown that the SDF-1/CXCL12 receptor, CXCR4, is also within MCH-expressing neurons confirming the hypothesis that SDF-1/CXCL12 could alter the feeding behavior by acting on its receptor expressed by MCH neurons in the rat LHA. Thus, by patch-clamp recordings of rat LHA slices, it was demonstrated that SDF-1/CXCL12 has a direct effect on voltage-dependent membrane currents of MCH neurons by decreasing or increasing peak and discharge frequency of action potentials, suggesting that SDF-1/CXCL12 may directly regulate MCH neuronal activity (Guyon et al. 2005). In addition, in the LHA, another chemokine, MCP-1/CCL2, co-localizes with MCH-expressing neurons, suggesting that MCP-1/CCL2 could also similarly act as a modulator of MCH neuronal activity (Banisadr et al. 2005b).

Chemokines and pituitary hormones

There is increasing evidence that the immune system-derived molecules can regulate the hormonal release directly at the pituitary level. Thus, it was shown that CINC stimulates prolactin and growth hormone secretions in a concentration-dependent manner. In the same study, it was also observed that CINC stimulates adrenocortico-trophin but not thyrotrophin secretion and that CINC suppresses the basal luteinizing hormone (LH) and follicle stimulating hormone (FSH) secretions from normal anterior pituitary cells in a dose-dependent manner (Sawada et al. 1994). Moreover, a recent study shows that CXCR4 mRNA is expressed in the rat pituitary adenoma cell line GH4C1 (a cell line that releases growth hormone) and that SDF-1 /CXCL12 causes both proliferation and growth hormone release, suggesting that the activation of CXCR4 may represent a novel regulatory mechanism for growth hormone secretion and pituitary cell proliferation, which may contribute to pituitary adenoma development (Florio et al. 2006).

Chemokines and water balance

An emerging concept recently arose from the observation that chemokines could be involved in water balance and expressed by arginine vasopressin (AVP) neurons in the PVN and SON of the hypothalamus. Indeed, it was previously demonstrated that the CINC is predominantly co-localized with AVP neurons in the SON (Sakamoto et al. 1996b). Moreover, after osmotic shock (induced by an i.p. injection of a hypertonic solution) that activates AVP neurons, CINC mRNA expression is rapidly up-regulated in the rat SON. A similar but much lower increase is also found in the PVN, mainly in its magnocellular subdivision of the PVN (Koike et al. 1997). In addition, our group has recently demonstrated by immunohistochemical studies that MCP-1/CCL2 is also constitutively expressed by AVP magnocellular neurons in the PVN and SON, notably in cell bodies and proximal processes, as well as in processes in the internal layer of the median eminence and in the posterior pituitary, suggesting a role of MCP-1/CCL2 in the neuroendocrine regulation of AVP-expressing neurons (Banisadr et al. 2005b).

Moreover, in another recent report, we investigated a possible neuroendocrine role of another chemokine: SDF-1/CXCL12. By means of dual fluorescent immunohistochemistry (Banisadr et al. 2003, Callewaere et al. 2006), we first demonstrated the co-localization of SDF-1/CXCL12 and its receptor CXCR4 with AVP neurons in the magnocellular neurons of the SON and PVN hypothalamic nuclei and on AVP projections in the median eminence (Fig. 1) to the neurohypophysis (Callewaere et al. 2006). Electrophysiological recordings of SON neurons clearly demonstrate that SDF-1/CXCL12 through its receptor CXCR4 affects the electrical activity of AVP neurons. The effect of SDF-1/CXCL12 results in changes in the bursting pattern of AVP neurons by either increasing the silences between bursts or inducing a constant stimulation of AVP neurons. Such changes in AVP neuronal electrical activity are known to result in the inhibition of AVP release (Fig. 2). Indeed, we observed that SDF-1/CXCL12 can blunt the autoregulation of AVP release in vitro and counteract angiotensin II-induced plasma AVP release in vivo. Furthermore, a short-term physiological increase in AVP release induced by enhanced plasma osmolarity produced by 1 M NaCl i.p. administration is similarly blocked by central injection of SDF-1/CXCL12 through its receptor CXCR4.

View larger version (65K): [in this window] [in a new window]   Figure 1 Immunohistochemical localization of SDF-1/CXCL12 (in green) with AVP (in red) in the internal layer of the normal rat median eminence.

View larger version (22K): [in this window] [in a new window]   Figure 2 Electrophysiological modulation of action potential firing of AVP neurons by 25 nM SDF-1/CXCL12 in the magnocellular part of the hypothalamic SON. In normal conditions, AVP neurons exhibit a bursting pattern characterized by periods of intense bursts and silences (A and B). Such periodic pattern is necessary for AVP release (Gouzenes et al. 1998). Following SDF-1/CXCL12 application on hypothalamic SON fragments, the firing pattern is modified. Thus, SDF-1/CXCL12 inhibits the activity of AVP neurons by increasing the silent periods (C) or stimulating the electrical neuronal activity (D). In both cases, it results in an inhibition of AVP release. Adapted from Callewaere et al.(2006).

View larger version (84K): [in this window] [in a new window]   Figure 3 Immunohistochemical localization of CXCR4 in the circumventricular organs: organ of the lamina terminalis (A) and subfornical organ (B). The circumventricular organs (CVO) located in the walls of the brain ventricular system and innervating the AVP neurons in the supraoptic and paraventricular nuclei detect changes in plasma osmolarity. It is thus possible that, similarly to what was observed in the magnocellular nuclei, SDF-1/CXCL12 in the CVO, through CXCR4, can modulate AVP release by autoregulating responses of CVO Angiotensin II neurons.

View larger version (25K): [in this window] [in a new window]   Figure 4 Schematic drawing representing the hypothalamic modulation of AVP release by SDF-1/CXCL12. In acute stimulation conditions, such as an increase in osmolarity or Angiotensin II, SDF-1/CXCL12 co-localized with AVP can be somatodendritically released and inhibit AVP release by an autoregulatory mechanism involving its receptor CXCR4. In conditions in which AVP is chronically stimulated, such as dehydration, SDF-1/CXCL12 is strongly released, resulting in a down-regulation of CXCR4. Such down-regulation of the receptor blocks the inhibitory effect of SDF-1/CXCL12 on AVP release, allowing a sustained increase in AVP secretion.

	Concluding remarks

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

	Acknowledgements

 
The authors declare that there is no conflict of interest that would prejudice the impartiality of this scientific work.

	References

Top Abstract Background Chemokine and chemokine receptor... Structure of chemokines Chemokine-receptor interaction Chemokine receptor-mediated... Involvement of chemokines in... Concluding remarks References

 
Baggiolini M & Loetscher P 2000 Chemokines in inflammation and immunity. Immunology Today 21 418–420.[CrossRef][ISI][Medline]

Bajetto A, Barbero S, Bonavia R, Piccioli P, Pirani P, Florio T & Schettini G 2001 Stromal cell-derived factor-1alpha induces astrocyte proliferation through the activation of extracellular signal-regulated kinases 1/2 pathway. Journal of Neurochemistry 77 1226–1236.[CrossRef][ISI][Medline]

Banisadr G, Skrzydelski D, Kitabgi P, Rostene W & Parsadaniantz SM 2003 Highly regionalized distribution of stromal cell-derived factor-1/CXCL12 in adult rat brain: constitutive expression in cholinergic, dopaminergic and vasopressinergic neurons. European Journal of Neuroscience 18 1593–1606.[CrossRef][ISI][Medline]

Banisadr G, Rostene W, Kitabgi P & Parsadaniantz SM 2005a Chemokines and brain functions. Current Drug Targets Inflammation Allergy 4 387–399.

Banisadr G, Gosselin RD, Mechighel P, Kitabgi P, Rostene W & Parsadaniantz SM 2005b Highly regionalized neuronal expression of monocyte chemoattractant protein-1 (MCP-1/CCL2) in rat brain: evidence for its colocalization with neurotransmitters and neuropeptides. Journal of Comparative Neurology 489 275–292.[CrossRef][ISI][Medline]

Bleul CC, Farzan M, Choe H, Parolin C, Clark-Lewis I, Sodroski J & Springer TA 1996 The lymphocyte chemoattractant SDF-1 is a ligand for LESTR/fusin and blocks HIV-1 entry. Nature 382 829–833.[CrossRef][Medline]

Callewaere C, Banisadr G, Desarmenien MG, Mechighel P, Kitabgi P, Rostene WH & Melik Parsadaniantz S 2006 The chemokine SDF-1/CXCL12 modulates the firing pattern of vasopressin neurons and counteracts induced vasopressin release through CXCR4. PNAS 103 8221–8226.[Abstract/Free Full Text]

Clark-Lewis I, Schumacher C, Baggiolini M & Moser B 1991 Structure-activity relationships of interleukin-8 determined using chemically synthesized analogs. Critical role of NH2-terminal residues and evidence for uncoupling of neutrophil chemotaxis, exocytosis, and receptor binding activities. Journal of Biological Chemistry 266 23128–23134.[Abstract/Free Full Text]

Clark-Lewis I, Kim KS, Rajarathnam K, Gong JH, Dewald B, Moser B, Baggiolini M & Sykes BD 1995 Structure-activity relationships of chemokines. Journal of Leukocyte Biology 57 703–711.[Abstract]

Clore GM & Gronenborn AM 1995 Three-dimensional structures of alpha and beta chemokines. FASEB Journal 9 57–62.[Abstract]

Cocchi F, DeVico AL, Garzino-Demo A, Arya SK, Gallo RC & Lusso P 1995 Identification of RANTES, MIP-1 alpha, and MIP-1 beta as the major HIV-suppressive factors produced by CD8+T cells. Science 270 1811–1815.[Abstract/Free Full Text]

Davatelis G, Wolpe SD, Sherry B, Dayer JM, Chicheportiche R & Cerami A 1989 Macrophage inflammatory protein-1: a prostaglandin-independent endogenous pyrogen. Science 243 1066–1068.[Abstract/Free Full Text]

Feng Y, Broder CC, Kennedy PE & Berger EA 1996 HIV-1 entry cofactor: functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor. Science 272 872–877.[Abstract]

Floridi F, Trettel F, Di Bartolomeo S, Ciotti MT & Limatola C 2003 Signalling pathways involved in the chemotactic activity of CXCL12 in cultured rat cerebellar neurons and CHP100 neuroepithelioma cells. Journal of Neuroimmunology 135 38–46.[CrossRef][ISI][Medline]

Florio T, Casagrande S, Diana F, Bajetto A, Porcile C, Zona G, Thellung S, Arena S, Pattarozzi A, Corsaro A et al. 2006 Chemokine stromal cell-derived factor 1alpha induces proliferation and growth hormone release in GH4C1 rat pituitary adenoma cell line through multiple intracellular signals. Molecular Pharmacology 69 539–546.[Abstract/Free Full Text]

Ganju RK, Dutt P, Wu L, Newman W, Avraham H, Avraham S & Groopman JE 1998a Beta-chemokine receptor CCR5 signals via the novel tyrosine kinase RAFTK. Blood 91 791–797.[Abstract/Free Full Text]

Ganju RK, Brubaker SA, Meyer J, Dutt P, Yang Y, Qin S, Newman W & Groopman JE 1998b The alpha-chemokine, stromal cell-derived factor-1alpha, binds to the transmembrane G-protein-coupled CXCR-4 receptor and activates multiple signal transduction pathways. Journal of Biological Chemistry 273 23169–23175.[Abstract/Free Full Text]

Gouzenes L, Desarmenien MG, Hussy N, Richard P & Moos FC 1998 Vasopressin regularizes the phasic firing pattern of rat hypothalamic magnocellular vasopressin neurons. Journal of Neuroscience 18 1879–1885.[Abstract/Free Full Text]

Guyon A, Banisadr G, Rovere C, Cervantes A, Kitabgi P, Melik-Parsadaniantz S & Nahon JL 2005 Complex effects of stromal cell-derived factor-1 alpha on melanin-concentrating hormone neuron excitability. European Journal of Neuroscience 21 701–710.[CrossRef][ISI][Medline]

Jones SA, Moser B & Thelen M 1995 A comparison of post-receptor signal transduction events in Jurkat cells transfected with either IL-8R1 or IL-8R2. Chemokine mediated activation of p42/p44 MAP-kinase (ERK-2). FEBS Letters 364 211–214.[CrossRef][ISI][Medline]

Knall C, Young S, Nick JA, Buhl AM, Worthen GS & Johnson GL 1996 Interleukin-8 regulation of the Ras/Raf/mitogen-activated protein kinase pathway in human neutrophils. Journal of Biological Chemistry 271 2832–2838.[Abstract/Free Full Text]

Koike K, Sakamoto Y, Kiyama H, Masuhara K, Miyake A & Inoue M 1997 Cytokine-induced neutrophil chemoattractant gene expression in the rat hypothalamus by osmotic stimulation. Brain Research Molecular Brain Research 52 326–329.[Medline]

Licinio J, Wong ML & Gold PW 1992 Neutrophil-activating peptide-1/interleukin-8 mRNA is localized in rat hypothalamus and hippocampus. Neuroreport 3 753–756.[ISI][Medline]

Matsumoto K, Koike K, Miyake A, Watanabe K, Konishi K & Kiyama H 1997 Noxious stimulation enhances release of cytokine-induced neutrophil chemoattractant from hypothalamic neurosecretory cells. Neuroscience Research 27 181–184.[CrossRef][ISI][Medline]

Mellado M, Rodriguez-Frade JM, Aragay A, del Real G, Martin AM, Vila-Coro AJ, Serrano A, Mayor F Jr & Martinez AC 1998 The chemokine monocyte chemotactic protein 1 triggers Janus kinase 2 activation and tyrosine phosphorylation of the CCR2B receptor. Journal of Immunology 161 805–813.[Abstract/Free Full Text]

Mellado M, Vila-Coro AJ, Martinez C & Rodriguez-Frade JM 2001 Receptor dimerization: a key step in chemokine signaling. Cellular and Molecular Biology 47 575–582.[ISI][Medline]

Minano FJ & Myers RD 1991 Anorexia and adipsia: dissociation from fever after MIP-1 injection in ventromedial hypothalamus and preoptic area of rats. Brain Research Bulletin 27 273–278.[CrossRef][ISI][Medline]

Minano FJ, Sancibrian M, Vizcaino M, Paez X, Davatelis G, Fahey T, Sherry B, Cerami A & Myers RD 1990 Macrophage inflammatory protein-1: unique action on the hypothalamus to evoke fever. Brain Research Bulletin 24 849–852.[CrossRef][ISI][Medline]

Minano FJ, Sancibrian M & Myers RD 1991a Fever induced by macrophage inflammatory protein-1 (MIP-1) in rats: hypothalamic sites of action. Brain Research Bulletin 27 701–706.[CrossRef][ISI][Medline]

Minano FJ, Vizcaino M & Myers RD 1991b Hypothalamic indomethacin fails to block fever induced in rats by central macrophage inflammatory protein-1 (MIP-1). Pharmacology, Biochemistry, and Behavior 39 535–539.[CrossRef][ISI][Medline]

Minano FJ, Fernandez-Alonso A, Myers RD & Sancibrian M 1996 Hypothalamic interaction between macrophage inflammatory protein-1 alpha (MIP-1 alpha) and MIP-1 beta in rats: a new level for fever control? Journal of Physiology 491 209–217.[ISI][Medline]

Murphy PM 2002 International Union of Pharmacology. XXX. Update on chemokine receptor nomenclature. Pharmacological Reviews 54 227–229.[Abstract/Free Full Text]

Myers RD, Paez X, Roscoe AK, Sherry B & Cerami A 1993 Fever and feeding: differential actions of macrophage inflammatory protein-1 (MIP-1), MIP-1 alpha and MIP-1 beta on rat hypothalamus. Neurochemical Research 18 667–673.[CrossRef][ISI][Medline]

Oberlin E, Amara A, Bachelerie F, Bessia C, Virelizier JL, Arenzana-Seisdedos F, Schwartz O, Heard JM, Clark-Lewis I, Legler DF et al. 1996 The CXC chemokine SDF-1 is the ligand for LESTR/fusin and prevents infection by T-cell-line-adapted HIV-1. Nature 382 833–835.[CrossRef][Medline]

Plata-Salaman CR 1988 Food intake suppression by growth factors and platelet peptides by direct action in the central nervous system. Neuroscience Letters 94 161–166.[CrossRef][ISI][Medline]

Plata-Salaman CR & Borkoski JP 1994 Chemokines/intercrines and central regulation of feeding. American Journal of Physiology 266 R1711–R1715.

Proudfoot AE, Power CA, Hoogewerf AJ, Montjovent MO, Borlat F, Offord RE & Wells TN 1996 Extension of recombinant human RANTES by the retention of the initiating methionine produces a potent antagonist. Journal of Biological Chemistry 271 2599–2603.[Abstract/Free Full Text]

Reyes TM, Walker JR, DeCino C, Hogenesch JB & Sawchenko PE 2003 Categorically distinct acute stressors elicit dissimilar transcriptional profiles in the paraventricular nucleus of the hypothalamus. Journal of Neuroscience 23 5607–5616.[Abstract/Free Full Text]

Sakamoto Y, Koike K, Kiyama H, Konishi K, Watanabe K, Osako Y, Hirota K & Miyake A 1996a Endotoxin activates a chemokinergic neuronal pathway in the hypothalamo–pituitary system. Endocrinology 137 4503–4506.[Abstract]

Sakamoto Y, Koike K, Kiyama H, Konishi K, Watanabe K, Tsurufuji S, Bicknell RJ, Hirota K & Miyake A 1996b A stress-sensitive chemokinergic neuronal pathway in the hypothalamo–pituitary system. Neuroscience 75 133–142.[CrossRef][ISI][Medline]

Sawada T, Koike K, Kanda Y, Sakamoto Y, Nohara A, Ohmichi M, Hirota K & Miyake A 1994 In vitro effects of CINC/gro, a member of the interleukin-8 family, on hormone secretion by rat anterior pituitary cells. Biochemical and Biophysical Research Communications 202 155–160.[CrossRef][ISI][Medline]

Tavares E & Minano FJ 2000 RANTES: a new prostaglandin dependent endogenous pyrogen in the rat. Neuropharmacology 39 2505–2513.[CrossRef][ISI][Medline]

Tavares E & Minano FJ 2004 Differential sensitivities of pyrogenic chemokine fevers to CC chemokine receptor 5 antibodies. Fundamental and Clinical Pharmacology 18 163–169.[CrossRef][ISI][Medline]

Thibeault I, Laflamme N & Rivest S 2001 Regulation of the gene encoding the monocyte chemoattractant protein 1 (MCP-1) in the mouse and rat brain in response to circulating LPS and proinflammatory cytokines. Journal of Comparative Neurology 434 461–477.[CrossRef][ISI][Medline]

Vila-Coro AJ, Rodriguez-Frade JM, Martin De Ana A, Moreno-Ortiz MC, Martinez AC & Mellado M 1999 The chemokine SDF-1alpha triggers CXCR4 receptor dimerization and activates the JAK/STAT pathway. FASEB Journal 13 1699–1710.[Abstract/Free Full Text]

Vila-Coro AJ, Mellado M, Martin de Ana A, Lucas P, del Real G, Martinez AC & Rodriguez-Frade JM 2000 HIV-1 infection through the CCR5 receptor is blocked by receptor dimerization. PNAS 97 3388–3393.[Abstract/Free Full Text]

Walz DA, Wu VY, de Lamo R, Dene H & McCoy LE 1977 Primary structure of human platelet factor 4. Thrombosis Research 11 893–898.[CrossRef][ISI][Medline]

Wang JF, Park IW & Groopman JE 2000 Stromal cell-derived factor-1alpha stimulates tyrosine phosphorylation of multiple focal adhesion proteins and induces migration of hematopoietic progenitor cells: roles of phosphoinositide-3 kinase and protein kinase C. Blood 95 2505–2513.[Abstract/Free Full Text]

Wells TN, Power CA & Proudfoot AE 1998 Definition, function and pathophysiological significance of chemokine receptors. Trends in Pharmacological Sciences 19 376–380.[CrossRef][Medline]

Wong M & Fish EN 1998 RANTES and MIP-1alpha activate stats in T cells. Journal of Biological Chemistry 273 309–314.[Abstract/Free Full Text]

Wu VY, Walz DA & McCoy LE 1977 Purification and characterization of human and bovine platelet factor 4. Preparative Biochemistry 7 479–493.[ISI][Medline]

Yoshimura T, Matsushima K, Tanaka S, Robinson EA, Appella E, Oppenheim JJ & Leonard EJ 1987 Purification of a human monocyte-derived neutrophil chemotactic factor that has peptide sequence similarity to other host defense cytokines. PNAS 84 9233–9237.[Abstract/Free Full Text]

Zheng J, Thylin MR, Ghorpade A, Xiong H, Persidsky Y, Cotter R, Niemann D, Che M, Zeng YC, Gelbard HA et al. 1999 Intracellular CXCR4 signaling, neuronal apoptosis and neuropathogenic mechanisms of HIV-1-associated dementia. Journal of Neuroimmunology 98 185–200.[CrossRef][ISI][Medline]

Received in final form 8 January 2007
Accepted 15 January 2007
Made available online as an Accepted Preprint 23 January 2007

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