Probing nano‐organization of astroglia with multi‐color super‐resolution microscopy. Issue 11 (2nd February 2017)

• Record Type: Journal Article
• Authors: Heller, Janosch P.; Michaluk, Piotr; Sugao, Kohtaroh; Rusakov, Dmitri A.
• Other Names: Schousboe Arne guestEditor.; Yu Albert C. H. guestEditor.; McKenna Mary C. guestEditor.
• Is Part Of: Journal of neuroscience research. Volume 95:Issue 11(2017)
• Page Start: 2159
• Page End: 2171
• Publication Date: 2017-02-02
• Subjects: Astroglia -- dSTORM -- super‐resolution microscopy -- GFAP -- S100β -- glutamine synthetase -- lck‐GFP -- pHluorin; Neurobiology -- Periodicals; 612
• DOI: 10.1002/jnr.24026
• Languages: English
• ISSNs: 0360-4012

Abstract

Abstract : Astroglia are essential for brain development, homeostasis, and metabolic support. They also contribute actively to the formation and regulation of synaptic circuits, by successfully handling, integrating, and propagating physiological signals of neural networks. The latter occurs mainly by engaging a versatile mechanism of internal Ca 2+ fluctuations and regenerative waves prompting targeted release of signaling molecules into the extracellular space. Astroglia also show substantial structural plasticity associated with age‐ and use‐dependent changes in neural circuitry. However, the underlying cellular mechanisms are poorly understood, mainly because of the extraordinary complex morphology of astroglial compartments on the nanoscopic scale. This complexity largely prevents direct experimental access to astroglial processes, most of which are beyond the diffraction limit of optical microscopy. Here we employed super‐resolution microscopy (direct stochastic optical reconstruction microscopy; dSTORM), to visualize astroglial organization on the nanoscale, in culture and in thin brain slices, as an initial step to understand the structural basis of astrocytic nano‐physiology. We were able to follow nanoscopic morphology of GFAP‐enriched astrocytes, which adapt a flattened shape in culture and a sponge‐like structure in situ, with GFAP fibers of varied diameters. We also visualized nanoscopic astrocytic processes using the ubiquitous cytosolic astrocyte marker proteins S100β and glutamine synthetase. Finally, we overexpressed and imaged membrane‐targeted pHluorin and lymphocyte‐specific protein tyrosine kinase (N‐terminal domain) ‐green fluorescent protein (lck‐GFP), to better understand the molecular cascades underlying some common astroglia‐targeted fluorescence imaging techniques. The results provide novel, albeit initial, insights into the cellular organization of astroglia on the nanoscale, paving the way for function‐specific studies. © 2017 Wiley Periodicals, Inc. Abstract : We employed direct stochastic optical reconstruction microscopy (dSTORM), to visualize astroglial organization on the nanoscale, in culture, and in thin brain slices, as an initial step to understand the structural basis of astrocytic nano‐physiology.