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Review
. 2015 Dec;63(12):2133-51.
doi: 10.1002/glia.22821. Epub 2015 Mar 18.

Morphological plasticity of astroglia: Understanding synaptic microenvironment

Janosch P Heller  1 , Dmitri A Rusakov  1
Affiliations
Review

Morphological plasticity of astroglia: Understanding synaptic microenvironment

Janosch P Heller et al. Glia. 2015 Dec.

Abstract

Memory formation in the brain is thought to rely on the remodeling of synaptic connections which eventually results in neural network rewiring. This remodeling is likely to involve ultrathin astroglial protrusions which often occur in the immediate vicinity of excitatory synapses. The phenomenology, cellular mechanisms, and causal relationships of such astroglial restructuring remain, however, poorly understood. This is in large part because monitoring and probing of the underpinning molecular machinery on the scale of nanoscopic astroglial compartments remains a challenge. Here we briefly summarize the current knowledge regarding the cellular organisation of astroglia in the synaptic microenvironment and discuss molecular mechanisms potentially involved in use-dependent astroglial morphogenesis. We also discuss recent observations concerning morphological astroglial plasticity, the respective monitoring methods, and some of the newly emerging techniques that might help with conceptual advances in the area.

Keywords: astrocyte plasticity; perisynaptic astrocytic processes; super-resolution microscopy.

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Figures

Figure 1
Figure 1
Astrocytes express various receptor types in their perisynaptic processes. (A) Silver‐enhanced (small grains) glutamine synthetase‐positive glial processes in the stratum lacunosum‐moleculare of CA1 region of the hippocampus. Finger‐like extensions of the glial processes at both sides of the spine (arrows) isolating these synaptic structures from the surrounding neuropil. s: spine. Adapted from (Derouiche and Frotscher, 1991). (B) Extremely fine PAPs (<100 nm, small arrows) ensheating pre‐ and/or postsynaptic elements (bold arrow in B1 pointing at synaptic cleft); mGluR2/3 (B1) and mGluR5 (B2) are present close to the synapse. Adapted from (Lavialle et al., 2011). (C) Double‐immunogold labeling of Kir4.1 (small particles, arrows) and aquaporin 4 (large particles) in vitreal perisynaptic Müller cell membranes (denoted M) surrounding photoreceptor terminals (Pt). Adapted from (Nagelhus et al., 1999). (D) Double labeling of astrocytic processes demonstrating co‐localization of GLT‐1 (small particles) and GLAST (large particles) (*) in rat hippocampus. S: dendritic spines; t: nerve terminals. Adapted from (Haugeto et al., 1996). Scale bars: 0.5 µm (B), 0.5 µm (C), 0.3 µm (D).
Figure 2
Figure 2
Varied morphology of astrocyte types. (A) Protoplasmic astrocyte in the mouse neocortex with numerous processes. (B) Bergmann glial cells from the mouse cerebellum. Note cell bodies are localized at one end, and distal process endings contacting the pia mater. (C) Müller cells of the mouse retina span the entire distance between the vitreous body and the retinal pigment epithelium. (A–C) adapted from (Reichenbach et al., 2010). (D) The degree of ramification of protoplasmic astrocytes at PND7 (D1), PND14 (D2), PND 21 (D3), and at 1 month (D4). Adapted from (Bushong et al., 2004). (E) Three‐dimensional reconstruction of astrocytes in the dentate gyrus. The yellow zone shows the border area where cellular processes of two adjacent astrocytes interdigitate. Adapted from (Wilhelmsson et al., 2006). (F) Schematic representation of functional synaptic islands. Different neuronal compartments can potentially be modulated by different astrocytes (F1). A group of dendrites from several neurons are enwrapped by a single astrocyte. Synapses localized within the territory of this astrocyte could potentially be affected in a coordinated manner by this glial cell (F2). Adapted from (Halassa et al., 2007b). (G) Double labeling of an acutely isolated (G1) and a cultured (G2) astrocyte for GFAP (red) and ezrin (green). Adapted from (Derouiche and Frotscher, 2001; Reichenbach et al., 2010). Scale bars: 20 µm (A), 5 µm (D), 15 µm (G1), 10 µm (G2).
Figure 3
Figure 3
Morphological diversity of astroglia within and among species. (A) Laminar astrocytes are present in human cortical layer 1, and the cells extend long processes through layers 2 to 4. Protoplasmic astrocytes can be found in layers 2 to 6. Varicose projection astrocytes are located in layers 5 and 6 from where they extend mm‐long processes with regularly spaced varicosities. Fibrous astrocytes reside in the white matter. (B1) Main processes of mouse protoplasmic astrocytes (inset) are less extended and developed than human astroglia (main image). (B2) Accordingly, fine processes and the entire morphology of astrocytes in mice correspond to much smaller functional islands (inset) compared with human astroglia (main image). Scale bars: 150 µm (A), 20 µm (B); Adapted from (Oberheim et al., 2009).
Figure 4
Figure 4
Astroglial coverage of excitatory synapses in three hippocampal areas. (A1) Three‐dimensional EM reconstruction of a single astroglial process (blue) in contact with four reconstructed dendrites (gold, yellow, red, purple) in hippocampal area CA1. (A2) Mushroom spine example with ∼50% circumvent contacted by astroglia (arrows). (A3) Thin dendritic spine example, with its neck adjacent to astroglia (arrows). Scale bar in A3 applies to A2‐3. Adapted from (Witcher et al., 2007). (B) Three‐dimensional EM reconstruction showing the astrocytic processes (green outlines) that surround a giant mossy fiber synapse in hippocampal area CA3, including the axonal bouton (yellow), the postsynaptic dendrite (de), and postsynaptic spiny excrescences (se, light blue). Fine astrocytic protrusions cover presynaptic and postsynaptic structures but do not reach synaptic active zones (red) on spiny excrescences; asterisk (void), location of an adjacent axonal bouton (not shown). Adapted from (Rollenhagen et al., 2007). (C) Three‐dimensional reconstruction of an astrocyte fragment (blue) shown with and without adjacent thin (left, grey) and mushroom (right, dark yellow) dendritic spines equipped with PSDs (red). Adapted from (Medvedev et al., 2014).
Figure 5
Figure 5
Advancing super‐resolution microscopy for astroglial research. (A) STED images showing CA1 stratum radiatum astrocytic processes (green, whole‐cell loading with Alexa Fluor 488) adjacent to synaptic structures in organotypic slices (red; Thy1‐YFP; dendritic spines, arrows) at lower (A1) and higher (A2, area indicted by square in A1) magnification; asterisk, O‐ring structures indicating tentative cell process envelopes; adapted from (Panatier et al., 2014). (B) STED image of P2Y1 receptors (red) along a multi‐branched astrocytic process (glutamine synthase, grey) in the adult mouse hippocampus. Adapted from (Volterra et al., 2014). (C) STORM imaging of pre‐ (Bassoon; red) and postsynaptic (Homer1; green) scaffolding proteins in the mouse main olfactory bulb glomeruli imaged using conventional fluorescence imaging (C1) and STORM (C2); adapted from (Dani et al., 2010). (D, E) dSTORM images of cultured (14 DIV) mixed glial cells from rat hippocampus (ProLong Diamond in Zeiss Elyra PS.1 microscope; Fiji Plugin ThunderSTORM, 3,000 frames); unpublished data by J. Heller. (D) GFAP stained with monoclonal antibody (Novus, GA5, secondary Alexa Fluor 488 donkey anti‐mouse antibody, Life Technologies) shown at lower (D1) and higher (D2, fragment indicated in D1) magnification. (E) GLT‐1 (polyclonal, Millipore) visualized with Alexa Fluor 568 goat anti‐guinea pig antibody (Life Technologies) shown at lower (E1) and higher (E2, fragment indicated in E1) magnification. Note that the cells were permeabilized, and therefore GLT‐1 was stained throughout cellular compartments.
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