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      Quantitating the subtleties of microglial morphology with fractal analysis

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          Abstract

          It is well established that microglial form and function are inextricably linked. In recent years, the traditional view that microglial form ranges between “ramified resting” and “activated amoeboid” has been emphasized through advancing imaging techniques that point to microglial form being highly dynamic even within the currently accepted morphological categories. Moreover, microglia adopt meaningful intermediate forms between categories, with considerable crossover in function and varying morphologies as they cycle, migrate, wave, phagocytose, and extend and retract fine and gross processes. From a quantitative perspective, it is problematic to measure such variability using traditional methods, but one way of quantitating such detail is through fractal analysis. The techniques of fractal analysis have been used for quantitating microglial morphology, to categorize gross differences but also to differentiate subtle differences (e.g., amongst ramified cells). Multifractal analysis in particular is one technique of fractal analysis that may be useful for identifying intermediate forms. Here we review current trends and methods of fractal analysis, focusing on box counting analysis, including lacunarity and multifractal analysis, as applied to microglial morphology.

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          NIH Image to ImageJ: 25 years of image analysis.

          For the past 25 years NIH Image and ImageJ software have been pioneers as open tools for the analysis of scientific images. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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            Reactive microgliosis.

            Damage to the central nervous system (CNS) elicits the activation of both astrocytes and microglia. This review is focused on the principal features that characterize the activation of microglia after CNS injury. It provides a critical discussion of concepts regarding microglial biology that include the relationship between microglia and macrophages, as well as the role of microglia as immunocompetent cells of the CNS. Mechanistic and functional aspects of microgliosis are discussed primarily in the context of microglial neuronal interactions. The controversial issue of whether reactive microgliosis is a beneficial or a harmful process is addressed, and a resolution of this dilemma is offered by suggesting different interpretations of the term 'activated microglia' depending on its usage during in vivo or in vitro experimentation.
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              Glial activation: a driving force for pathological pain.

              Pain is classically viewed as being mediated solely by neurons, as are other sensory phenomena. The discovery that spinal cord glia (microglia and astrocytes) amplify pain requires a change in this view. These glia express characteristics in common with immune cells in that they respond to viruses and bacteria, releasing proinflammatory cytokines, which create pathological pain. These spinal cord glia also become activated by certain sensory signals arriving from the periphery. Similar to spinal infection, these signals cause release of proinflammatory cytokines, thus creating pathological pain. Taken together, these findings suggest a new, dramatically different approach to pain control, as all clinical therapies are focused exclusively on altering neuronal, rather than glial, function.
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                Author and article information

                Journal
                Front Cell Neurosci
                Front Cell Neurosci
                Front. Cell. Neurosci.
                Frontiers in Cellular Neuroscience
                Frontiers Media S.A.
                1662-5102
                30 January 2013
                2013
                : 7
                : 3
                Affiliations
                [1] 1Centre for Research in Complex Systems, School of Community Health, Charles Sturt University Albury, NSW, Australia
                [2] 2Institute of Biophysics, Medical University of Graz Graz, Austria
                [3] 3Rural Clinical School, University of New South Wales Sydney, NSW, Australia
                Author notes

                Edited by: Marie-Eve Tremblay, Université Laval, Canada

                Reviewed by: Hermann Cuntz, Ernst Strüngmann Institute, Germany; Denis Soulet, Laval University, Canada

                *Correspondence: Audrey Karperien, Centre for Research in Complex Systems, School of Community Health, Charles Sturt University, Albury, NSW 2640, Australia. e-mail: akarpe01@ 123456postoffice.csu.edu.au
                Article
                10.3389/fncel.2013.00003
                3558688
                23386810
                fb2ba9b1-4cc9-4a14-a434-444a158c803d
                Copyright © 2013 Karperien, Ahammer and Jelinek.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 26 November 2012
                : 08 January 2013
                Page count
                Figures: 7, Tables: 0, Equations: 4, References: 160, Pages: 18, Words: 16598
                Categories
                Neuroscience
                Review Article

                Neurosciences
                box counting,cell shape,fractals,image interpretation: computer-assisted,lacunarity,microglia,models: biological,multifractal analysis

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