The development of the CNS (central nervous system) necessitated an increase in cell specialization, so that neurons, although perfecting sophisticated machinery for rapid propagation of information through electrically excitable membrane and synaptic contacts, lost their metabolic independence. This became possible by a parallel phylogenetic advance of the neuroglia, which assumed the function of a primary brain homoeostatic and defence cellular system (Giaume et al., 2007; Reichenbach and Pannicke, 2008). At the later evolutionary stages, in the primates and human brain, the neuroglia became specifically developed. Indeed, both the number and structural complexity of the astrocytes (the principal neuroglial cells in the grey matter) is substantially higher in primates as compared with other species; astrocytes in the human brain are the most numerous and complex among the whole of the animal kingdom (Oberheim et al., 2006; Sherwood et al., 2006; Oberheim et al., 2009; Verkhratsky, 2009).

The processes of astroglia form excessively intricate arborizations, which, by virtue of tiny appendages and membranous expansions (Grosche et al., 1999), provide a tight coverage for a majority of synapses in the CNS, thus forming the tripartite synaptic structure (Araque et al., 1999; Perea et al., 2009). On average a single astrocyte in the brain of rodents covers ∼100 000 synapses, whereas the human astrocyte embraces up to 2 000 000 synaptic contacts (Oberheim et al., 2006). As a result, a single astrocyte perceives and most likely integrates the massive synaptic input. The signalling input to the astroglia is mediated by numerous receptors expressed in astrocytes, the expression being greatly heterogeneous in different astroglial cells, and being finely tuned by the immediate neurotransmitter environment (Verkhratsky et al., 1998; Verkhratsky and Steinhauser, 2000). The functional relevance of astroglial information processing for higher cognitive functions is virtually unknown, yet its importance for brain homoeostasis is fundamental. Indeed the astrocytes are central elements of the neurovascular unit, and astrocytes couple the neuronal activity with local blood flow and metabolic support of neuronal networks (Zonta et al., 2003; Magistretti, 2006).

An increase in complexity of neural networks evolved in parallel with intercellular signalling, which relies upon neurotransmitters and neuromodulators. The primitive forms of extracellular signalling had already appeared in prokaryotes, in which two main extracellular transmitter molecules, ATP and glutamate, acted as danger signals (Burnstock and Verkhratsky, 2009). Further developments led to an ever-increased variety of neurotransmitter molecules and neurotransmitter receptors, and their functional segregation between brain regions.

Astroglial receptors are many; astrocytes express both ionotropic and GPCRs (G-protein-coupled metabotropic receptors). The functional role of ionotropic astroglial receptors remains somewhat obscure, as indeed their activation hardly can have electric consequences, and is probably mediated by localized ion fluxes with subsequent formation of cytosolic domains of high Ca²⁺ or Na⁺. The glial metabotropic receptors, in contrast, are directly connected to the glial Ca²⁺ excitability mediated through intracellular signalling cascades and Ca²⁺-release channels of the endoplasmic reticulum membrane (Verkhratsky et al., 1998; Verkhratsky, 2006). The metabotropic signalling is controlled by a balance between plasmalemmal and intracellular distribution of the GPSRc, which can be dynamically shifted, thus affecting the efficacy of the signalling chain. Furthermore, a remarkable complexity of astroglial processes, which come into contact with multiple synapses, calls for a precise control of allocation of various receptors, which can rapidly change depending on the levels of synaptic input. All of the above contemplations are, however, in a purely speculative realm, because of the absence of specific approaches allowing real-time tracking of receptor movements in glial cells. In this issue of ASN NEURO, Osborne et al. (2009) have presented a new and fundamentally important technique of real-time imaging of receptor movements inside astroglial cells. They chose to genetically label the CB1R (cannabinoid receptor 1) with green fluorescent protein, which, upon expression in cortical astrocytes, can be imaged with fluorescent video-microscopy. The CB1Rs are typical GPCRs that are constitutively expressed in astroglia and are involved in various forms of signalling in neuronal–glial circuits (Navarrete and Araque, 2008).

The fluorescent CB1R chimeras were concentrated in the intracellular vesicles, some of which were actively transported to the plasmalemma with the help of cytoskeletal elements. This transport can be of fundamental importance, as it may dynamically enrich the specific regions of the astroglial processes [e.g. the end-foot structures where CB1Rs are preferentially located (Rodriguez et al., 2001)], with the receptors thus providing a mechanism for controlling local signalling events. The obvious perspective developments are the insertion of chimeric fluorescently labelled receptors of various kinds in glial cells in vivo, which opens a whole range of new possibilities for dynamic imaging of receptor distribution and trafficking, and the role of these processes in controlling information processing in neuronal–glial networks.