Professor A. Verkhratsky, Faculty of Life Sciences, The University of Manchester, 1.124 Stopford Building, Oxford Road, Manchester M13 9PT, UK. T: + 44 (0)161 2755414; F: + 44 (0)161 275 5948; E: email@example.com
The brain is the most complex organ of the human body. It is composed of several highly specialized and heterogeneous populations of cells, represented by neurones (e.g. motoneurons, projection neurons or interneurons), and glia represented by astrocytes, oligodendrocytes and microglia. In recent years there have been numerous studies demonstrating close bidirectional communication of neurons and glia at structural and functional levels. In particular, the excitatory transmitter glutamate has been shown to evoke a variety of responses in astrocytes and oligodendrocytes in the healthy as well as the diseased brain. Here we overview the multitude of glutamate sensing molecules expressed in glia and describe some general experiments which have been performed to identify the glutamate-responsive molecules, i.e. the ionotropic and metabotropic glutamate receptors as well as the glutamate transporters. We also discuss a transgenic mouse model that permits detailed and specific investigations of the role of glial glutamate receptors.
Probably the first contemplation of glutamate as an excitatory transmitter in the central nervous system was made by Hayashi (1954), based on his findings that injection of glutamate in the brain provokes convulsions. By that time it was well known that glutamate is present in the nervous system at very high concentrations, yet it was firmly believed that glutamate is primarily involved with brain metabolism, rather then with synaptic transmission. The first direct experiment, which gave birth to the theory of glutamatergic transmission, was reported by Curtis et al. (1959), who discovered that iontophoretically delivered glutamate excited neurons in the spinal cord; they, however, found that other amino acids had the same ability and concluded that glutamate was most probably a non-specific agent not connected with interneuronal signalling. This view of non-specificity of glutamate prevailed for almost 20 years, before the appearance of specific agonists and antagonists helped to identify neuronal glutamate receptors (Evans et al. 1979; Watkins & Evans, 1981). In the ensuing 25 years the concept of glutamate as a main excitatory neurotransmitter in the brain was fully developed.
Incidentally, glutamate excites not only neurons but also glial cells, which became apparent in 1984 when microelectrode recordings revealed glutamate-mediated depolarization of astrocytes and oligodendrocytes (Bowman & Kimelberg, 1984; Kettenmann et al. 1984a,b). Further experiments have clearly demonstrated that glutamate acts as a mediator of both interneuronal and neuronal–glial signalling.
Overall, the glial cells interact with glutamate through three distinct molecular systems (Fig. 1), represented by ionotropic and metabotropic glutamate receptors as well as glutamate transporters. This review provides a concise overview of the diverse glutamate signalling pathways within the various glial cell types.
Ionotropic glutamate receptors
Three families of ionotropic glutamate receptors, defined by specific pharmacology and with distinct molecular structures, are present in the nervous system. These three families are AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid), kainate and NMDA (N-methyl-d-aspartate) receptors, which all belong to a broad family of cationic ligand-operated channels (for reviews see Wisden & Seeburg, 1993; Mayer & Armstrong, 2004; Mayer, 2005). All three families are expressed and functionally operational in the brain glia, although their distribution shows remarkable region- and cell-type specificity.
The second type of glutamate receptors, the kainate receptor, is assembled from five distinct subunits, the KA1 and KA2 and GluR5–7 (Huettner, 2003; Lerma, 2003). All these subunits were identified in certain types of astroglial cells (e.g. in bovine corpus callosum or in rodent perivascular astrocytes) at either the mRNA or the protein level (Garcia-Barcina & Matute, 1996; Brand-Schieber et al. 2004). Unfortunately, we still lack the evidence for functional kainate receptors determined as ion fluxes through the receptor pore. Incidentally, the GluR5 receptors are important for astroglial–neuronal signalling in hippocampus, where glutamate, released from the astroglia, signals to inhibitory neurons precisely through activation of neuronal GluR5 kainate receptors (Frerking, 2004; Liu et al. 2004). Kainate receptors were also identified in oligodendrocytes, where they may be important for mediating glutamate excitotoxicity (Alberdi et al. 2005, 2006).
The third type of glutamate receptor are the NMDA receptors encoded by seven genes, NR1, NR2A–D, and NR3A and B (Kew & Kemp, 2005). Similar to the AMPA or kainate receptors a heteromeric assembly of four subunits forms the ion-permeating pore of the NMDA receptor. The NR1 subunit is essential. NR2 or NR3 subunits alone are not sufficient to form a functional channel. NMDA receptors were for a long-time considered to be specifically confined to neurons. NMDA receptors display several important features, which conceptually made them relevant for neuronal integration and regulation of synaptic plasticity. These features include a very high Ca2+ permeability (PCa/PNa > 10; Mori & Mishina, 1995) and a specific Mg2+-dependent voltage-dependent block, which renders NMDA receptors barely active at hyperpolarized (–80 to –70 mV) membrane potentials (Mayer et al. 1984; Nowak et al. 1984). As a consequence, NMDA-mediated Ca2+ fluxes occur only when Mg2+ block is removed by sufficient depolarization of neurons, which provides for coincidence detection, relevant for various forms of synaptic plasticity (Collingridge & Bliss, 1995). As glial cells typically maintain a high degree of membrane polarization (resting potential ~ –80 mV) and are almost devoid of depolarizing ion permeabilities, it was firmly believed that NMDA receptors do not have any room for operation. Yet some time ago NMDA receptors subunits were detected in several types of astrocytes by immunohistochemistry, RT-PCR or in situ hybridization. In addition, NMDA-induced Ca2+ and membrane current responses were recorded from astroglia (e.g. Muller et al. 1993; Conti et al. 1996, 1997, 1999; Ziak et al. 1998; Schipke et al. 2001). Very recently, a series of papers substantiated the presence of functional NMDA receptors in cortical astrocytes (Fig. 3; Lalo et al. 2006) and demonstrated NMDA receptor expression and their fatal involvement in ischaemic insults in oligodendrocytes (Karadottir et al. 2005; Salter & Fern, 2005; Micu et al. 2006). Interestingly, in hippocampal astrocytes an up-regulation of the NMDA receptor subunit NR2B could be detected a few days after ischaemia and anoxia (Krebs et al. 2003). Incidentally, glial NMDA receptors are much less sensitive to Mg2+ block, which may result from a specific molecular composition (Lipton, 2006) being, as result, perfectly operational at the glial resting potentials.
All in all, glial cells have a wide complement of ionotropic glutamate receptors, which have different sensitivity to glutamate, different kinetics and different ion permeability properties, thus allowing glial cells a high degree of sophistication in deciphering signals carried by external glutamate.
Metabotropic glutamate receptors
Metabotropic glutamate receptors are abundantly present in glial cells. These receptors, represented by eight different genes (mGluR1–8), belong to the family of seven-transmembrane-domain, G-protein-coupled receptors (Nakanishi, 1994; Kew & Kemp, 2005; Ferraguti & Shigemoto, 2006). Metabotropic glutamate receptors 1 and 5 (also known as group I mGluRs) are functionally linked to phospholipase C and synthesis of 1,4,5-inositol-trisphosphate (InsP3) and diacylglycerol (DAG); by contrast, mGluRs 2 and 3 (group II) and mGluRs 4 and 6–8 (Group III) are coupled to adenylate cyclase. Although it is assumed that glial cells can express all types of mGluRs, mGluR 3 and 5 remain the most abundant and best characterized glial mGluRs. These two types of mGluRs were also identified in situ, in astroglial processes at the ultrastructural level (Petralia et al. 1996; Aronica et al. 2000; Tamaru et al. 2001). Immunohistochemical identification of mGluR subtypes in oligodendroglia has not yet been shown. Both mGluR 3 and 5 could be demonstrated on cultured oligodendrocyte progenitor cells by Western blot analysis (Deng et al. 2004). Functionally, the group I mGluRs are important for triggering cytosolic Ca2+ signalling through stimulation of InsP3-induced Ca2+ release from the endoplasmic reticulum (ER) calcium store (Verkhratsky, 2005). Conceptually, the ER calcium store acts as a main source for glial calcium signalling; furthermore, it forms an intracellular excitable medium, which is instrumental for generation of long-range propagating glial Ca2+ waves (Verkhratsky & Kettenmann, 1996; Verkhratsky et al. 1998; Verkhratsky, 2006b). Stimulation of mGluR5 triggers elevation of cytosolic Ca2+ concentration in glia; these Ca2+ signals do not require extracellular Ca2+ and are sensitive to inhibitors of ER Ca2+ accumulation (thapsigargin or cyclopiazonic acid) and to heparin, which blocks InsP3 receptors residing in the ER membrane (Fig. 4; Kirischuk et al. 1999). Furthermore, at least in Bergmann glial cells, the mGluRs represent the main route for Ca2+ signal generation, as Ca2+ entry through AMPA receptors is limited by rapid desensitization of the receptors when activated by glutamate (cf. Fig. 2; Kirischuk et al. 1999).
Glutamate transporters and glial Na+ homeostasis
Astroglial cells represent the main sink of glutamate in the brain. From the bulk of glutamate released during synaptic transmission, about 20% is accumulated into postsynaptic neurons and the remaining 80% is taken up by perisynaptic astrocytes (Swanson, 2005). This transport is achieved by specific glutamate transporters, represented, in the human brain, by five types, classified as EAAT1 to EAAT5 (where EAAT stands for excitatory amino acid transporter). EAAT1 and EAAT2 (analogues of which in rodent brain are known as glutamate/aspartate transporter, GLAST, and glutamate transporter-1, GLT-1) are expressed almost exclusively in astrocytes (Danbolt, 2001). Translocation of glutamate is powered by transmembrane ion gradients, and transport of a single glutamate molecule requires influx of three Na+ ions and one H+ ion together with efflux of one K+ ion. As a result Na+/glutamate transporter has an electrogenic effect, manifested in a net inward sodium current, and may substantially affect intracellular Na+ concentration.
Future experimental strategies: astroglia-specific and inducible gene deletion
Many studies have been performed to investigate the repertoire of glutamate signalling in glial cells. It has been shown that glial cells are sophisticated sensors of the excitatory transmitter glutamate, which is achieved through various response pathways. Remarkably, glial cells do not necessarily express significantly different glutamate receptors than their neighbouring neurons. Therefore, it was almost impossible to analyse the unique contribution of a given receptor subunit expressed in glia to the function of the whole brain or the behaviour of the freely moving animal. Any pharmacological intervention would have immediately affected both cell types, neurons and glia.
Very recently a series of transgenic mice have been developed which allow the selective ablation of defined genes either in astrocytes or in oligodendrocytes. Transgenic mice were generated by oocyte injection (non-homologous recombination) of transgenes composed of the human glial fibrillary acidic protein (GFAP) promoter (to achieve astroglia-specific expression), the coding sequence for a fusion protein of the DNA recombinase Cre and the mutated ligand binding domain of the human oestrogen receptor (Fig. 5; Hirrlinger et al. 2006). A different mouse line has been generated by direct targeting (homologous recombination) of the CreERT2 coding sequence into the astroglia-specific locus of the glutamate transporter GLAST (Mori et al. 2006). Inducible recombination in myelinating glia (oligodendrocytes and Schwann cells) is also possible by using the TgN(PLP-CreERT2) mice in which CreERT2 is targeted by the mouse proteolipid protein promoter into oligodendrocytes (Doerflinger et al. 2003; Leone et al. 2003).
The transgenic CreERT2-mice can now be cross-bred to genetically modified mice in which relevant target genes, i.e. glutamate receptor genes, are flanked by loxP sites. The functional role of a given gene in a defined glial cell population can now be tested in the whole animal (e.g. by in vivo physiology or behavioural experiments) by temporal control of gene ablation via intraperitoneal injection of tamoxifen. Several mouse lines with appropriate modification of glutamate receptor genes are already available, for example to study different AMPA receptor genes GluR1–4 or the NR1 subunit of NMDA receptors (Tsien et al. 1996; Zamanillo et al. 1999). Unfortunately, similar models are not yet available for the metabotropic glutamate receptors.
Glutamate mediates neuronal–neuronal and neuronal–glial signalling. Synaptic release of glutamate triggers a complex response in glial cells, which involves activation of several distinct types of ionotropic and metabotropic receptors as well as glutamate transporters. These molecules, in turn, initiate a variety of intracellular signalling processes, most notably those associated with propagating cytoplasmic Ca2+ signals. Extended complement of glutamate sensors expressed in glial cell membranes allows the glia to decode neuronal activity and to synchronize and integrate neuronal and glial circuitries. Deployment of transgenic animal models with conditional deletion of single signalling components promises new discoveries of the pivotal functions of glial cells.
The research was supported by the National Institute of Health, the Royal Society, the Wellcome Trust, the Alzheimer Research Trust (UK), the Max Plank Society and Deutsche Forschungsgemeinschaft.