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Editorial



           Astrocytes: everything but the glue


           Oscar Gonzalez‑Perez , Veronica Lopez‑Virgen , Alfredo Quiñones‑Hinojosa 2
                              1
                                                    1
            1 Laboratory of Neuroscience, School of Psychology, University of Colima, Colima, Col 28040, Mexico.
           2 Department of Neurosurgery, Johns Hopkins School of Medicine, Baltimore, MD 21201, USA.


                                                                              [2]
           The current knowledge in neuroscience indicates that   communication.  Postnatal synapse refinement is
           the neural tissue has two major cell populations: neurons   also associated with astrocyte maturation suggesting
           and glia (term derived from the Greek word for glue).   that the astroglia is an important modulator of neuronal
           Neuronal population is characterized by the capacity to   plasticity. [3]
           produce action potentials, whereas glial cells are typically
           identified as the subordinate cell population of neurons.   Astrocytes are ubiquitous brain cells that outnumber
           Till date, this point of view has changed dramatically, and   neuronal population in the proportion of 10:1 and
           growing evidence indicates that glial cells play a crucial   comprise approximately 50% of the neural tissue. Before
           role in normal mental functions and the pathogenesis   1980’s, the role of astrocytes was basically associated
           of neurological diseases. Classically, glial cells include   with supporting and nourishing neurons (primarily
           four major populations clearly discernible in the adult’s   considered as a “real” functional cells). However,
           brain: astrocytes, oligodendrocytes, microglia cells and   current evidence  indicates that this  perspective  is
           NG2 glia. Astrocytes, also referred as to astroglia, are by   quite limited and incorrect. Today, it is well accepted
           far the most abundant cell lineage in the adult’s brain and   that astrocytes have a more major role in neurological
           display a very diverse morphology, which varies during   functioning, neural homeostasis and pathogenesis than
           neural development and adulthood [Figure 1]. These   previously thought. [4]
           cells are in close contact with several tissue components
           of the brain parenchyma including neurons, vasculature,   Astroglia is the main source of glycogen that
           extracellular matrix and other glial populations. Hence,   delivers energy to the brain interstitial tissue and
                                                                                                      [5]
           the number and strategic position of astrocytes provide   nourishes neurons by providing lactate.  Other
           them with exceptional capacity for modulating multiple   astrocytic functions include: the uptake or release
                                                                                    [6]
           functions in the neural tissue.                    of  neurotransmitters,   modulation  of  synaptic
                                                              plasticity and neuronal transmission,  regulation of
                                                                                                 [3]
           During neural development, the origin of astrocyte   interstitial ions,  cerebral regulation of blood flow
                                                                             [7]
           varies according to the anatomical region, but the   and blood-brain barrier,  myelin regulation,  tissue
                                                                                                       [9]
                                                                                    [8]
           most accepted viewpoint suggests that astrocytic cells   repair, [10]  neuroprotection [11]  and drug metabolism. [12]
           originate from radial glial cells (in the ventricular zone)
           and some progenitor cells located in the subventricular   In addition, astrocytes have astonishing enzymatic
           zone (SVZ). Therein, astrocyte lineage is directed by the   machinery that includes cyclooxygenase, lipoxygenase
           expression of notch receptors and their ligands (delta   and cytochrome P450 epoxygenase pathways. [12]
           and serrate-jagged) that efficiently repress neuronal   Remarkably, these enzymes allow astrocytes to depurate
                                     [1]
           fate and promotes gliogenesis.  At this developmental   several drugs and alcohol, a property that was previously
           stage, astrocytes are crucial for the synapse formation   thought to be exclusive of hepatocytes (liver cells).
           by improving the neuron’s ability to receive synaptic   Astroglia can also produce metabolic intermediates
           contacts, which consequently initiate neuronal     of polyunsaturated fatty acid arachidonic acid and
                                                              epoxide metabolites that may help protect against
                          Access this article online          stroke. Nevertheless, some gene mutations on astrocytes
               Quick Response Code:                           produce defective proteins that upon accumulation
                                    Website:                  may lead to neurodegenerative diseases. Besides, the
                                    www.nnjournal.net
                                                              phospholipase-C  (PLC) enzymatic family and the
                                    DOI:                      phosphoinositide signaling system are essential for
                                    10.4103/2347-8659.153979   molecule transduction from the cell membrane to
                                                              the nucleus. [12]  This system appears to be involved


           Corresponding Author: Dr. Oscar Gonzalez‑Perez, Laboratory of Neuroscience, School of Psychology, University of Colima, Av.
           Universidad 333, Colima, Col 28040, Mexico. E‑mail: osglez@ucol.mx



          Neuroimmunol Neuroinflammation | Volume 2 | Issue 2 | April 15, 2015                              115
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