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      Astrocytes Amplify Neuronal Dendritic Volume Transmission Stimulated by Norepinephrine

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          SUMMARY

          In addition to their support role in neurotransmitter and ion buffering, astrocytes directly regulate neurotransmission at synapses via local bidirectional signaling with neurons. Here, we reveal a form of neuronal-astrocytic signaling that transmits retrograde dendritic signals to distal upstream neurons in order to activate recurrent synaptic circuits. Norepinephrine activates α 1 adrenoreceptors in hypothalamic corticotropin-releasing hormone (CRH) neurons to stimulate dendritic release, which triggers an astrocytic calcium response and release of ATP; ATP stimulates action potentials in upstream glutamate and GABA neurons to activate recurrent excitatory and inhibitory synaptic circuits to the CRH neurons. Thus, norepinephrine activates a retrograde signaling mechanism in CRH neurons that engages astrocytes in order to extend dendritic volume transmission to reach distal presynaptic glutamate and GABA neurons, thereby amplifying volume transmission mediated by dendritic release.

          In Brief

          Norepinephrine is a primary driver of the stress response. Chen et al. show that norepinephrine activates hypothalamic CRH neurons by engaging a dendritic signaling mechanism that recruits astrocytes to activate upstream neurons. This retrograde neuronal-glial signaling allows neurons to control distal presynaptic partners via astrocyte amplification of dendritic volume transmission.

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          Most cited references63

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          Physiology of Astroglia.

          Astrocytes are neural cells of ectodermal, neuroepithelial origin that provide for homeostasis and defense of the central nervous system (CNS). Astrocytes are highly heterogeneous in morphological appearance; they express a multitude of receptors, channels, and membrane transporters. This complement underlies their remarkable adaptive plasticity that defines the functional maintenance of the CNS in development and aging. Astrocytes are tightly integrated into neural networks and act within the context of neural tissue; astrocytes control homeostasis of the CNS at all levels of organization from molecular to the whole organ.
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            Tripartite synapses: glia, the unacknowledged partner.

            According to the classical view of the nervous system, the numerically superior glial cells have inferior roles in that they provide an ideal environment for neuronal-cell function. However, there is a wave of new information suggesting that glia are intimately involved in the active control of neuronal activity and synaptic neurotransmission. Recent evidence shows that glia respond to neuronal activity with an elevation of their internal Ca2+ concentration, which triggers the release of chemical transmitters from glia themselves and, in turn, causes feedback regulation of neuronal activity and synaptic strength. In view of these new insights, this article suggests that perisynaptic Schwann cells and synaptically associated astrocytes should be viewed as integral modulatory elements of tripartite synapses.
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              Astrocytic purinergic signaling coordinates synaptic networks.

              To investigate the role of astrocytes in regulating synaptic transmission, we generated inducible transgenic mice that express a dominant-negative SNARE domain selectively in astrocytes to block the release of transmitters from these glial cells. By releasing adenosine triphosphate, which accumulates as adenosine, astrocytes tonically suppressed synaptic transmission, thereby enhancing the dynamic range for long-term potentiation and mediated activity-dependent, heterosynaptic depression. These results indicate that astrocytes are intricately linked in the regulation of synaptic strength and plasticity and provide a pathway for synaptic cross-talk.
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                Author and article information

                Journal
                101573691
                39703
                Cell Rep
                Cell Rep
                Cell reports
                2211-1247
                3 January 2020
                24 December 2019
                10 February 2020
                : 29
                : 13
                : 4349-4361.e4
                Affiliations
                [1 ]Department of Cell and Molecular Biology, Tulane University, New Orleans, LA 70118, USA
                [2 ]Tulane Brain Institute, Tulane University, New Orleans, LA 70118, USA
                [3 ]These authors contributed equally
                [4 ]Present address: Gladstone Institute of Neurological Disease, San Francisco, CA 94158, USA
                [5 ]Present address: Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, USA
                [6 ]Present address: Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA 94143, USA
                [7 ]Lead Contact
                Author notes
                [* ]Correspondence: tasker@ 123456tulane.edu

                AUTHOR CONTRIBUTIONS

                Conceptualization, J.G.T.; Methodology, J.G.T., H.H., C.C., and Z.J.; Investigation, C.C., Z.J., X.F., D.Y., and H.H.; Writing – Original Draft, Z.J. and C.C.; Writing – Review & Editing, J.G.T., C.C., and Z.J.; Visualization, C.C., Z.J., and J.G.T.; Supervision, J.G.T.; Project Administration, J.G.T.; Funding Acquisition, J.G.T.

                Article
                NIHMS1547523
                10.1016/j.celrep.2019.11.092
                7010232
                31875545
                793a450c-cfba-4864-b240-48af5ff195a1

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Cell biology
                Cell biology

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