Literature DB >> 31283900

Neuron-Glia Signaling in Synapse Elimination.

Daniel K Wilton1, Lasse Dissing-Olesen1, Beth Stevens1,2,3.   

Abstract

Maturation of neuronal circuits requires selective elimination of synaptic connections. Although neuron-intrinsic mechanisms are important in this process, it is increasingly recognized that glial cells also play a critical role. Without proper functioning of these cells, the number, morphology, and function of synaptic contacts are profoundly altered, resulting in abnormal connectivity and behavioral abnormalities. In addition to their role in synaptic refinement, glial cells have also been implicated in pathological synapse loss and dysfunction following injury or nervous system degeneration in adults. Although mechanisms regulating glia-mediated synaptic elimination are still being uncovered, it is clear this complex process involves many cues that promote and inhibit the removal of specific synaptic connections. Gaining a greater understanding of these signals and the contribution of different cell types will not only provide insight into this critical biological event but also be instrumental in advancing knowledge of brain development and neural disease.

Entities:  

Keywords:  astrocyte; disease; microglia; molecular mechanism; myelinating glia; neuronal activity; synaptic pruning

Mesh:

Year:  2019        PMID: 31283900     DOI: 10.1146/annurev-neuro-070918-050306

Source DB:  PubMed          Journal:  Annu Rev Neurosci        ISSN: 0147-006X            Impact factor:   12.449


  72 in total

Review 1.  Developmental neuromuscular synapse elimination: Activity-dependence and potential downstream effector mechanisms.

Authors:  Young Il Lee
Journal:  Neurosci Lett       Date:  2019-12-23       Impact factor: 3.046

2.  Engulfed by Glia: Glial Pruning in Development, Function, and Injury across Species.

Authors:  Stephan Raiders; Taeho Han; Nicole Scott-Hewitt; Sarah Kucenas; Deborah Lew; Mary A Logan; Aakanksha Singhvi
Journal:  J Neurosci       Date:  2021-01-19       Impact factor: 6.167

Review 3.  Mechanisms and significance of microglia-axon interactions in physiological and pathophysiological conditions.

Authors:  Yuki Fujita; Toshihide Yamashita
Journal:  Cell Mol Life Sci       Date:  2021-01-28       Impact factor: 9.261

4.  Inflammation of the Embryonic Choroid Plexus Barrier following Maternal Immune Activation.

Authors:  Jin Cui; Frederick B Shipley; Morgan L Shannon; Osama Alturkistani; Neil Dani; Mya D Webb; Arthur U Sugden; Mark L Andermann; Maria K Lehtinen
Journal:  Dev Cell       Date:  2020-10-09       Impact factor: 12.270

Review 5.  Potential Roles of Redox Dysregulation in the Development of Schizophrenia.

Authors:  Diana O Perkins; Clark D Jeffries; Kim Q Do
Journal:  Biol Psychiatry       Date:  2020-04-02       Impact factor: 13.382

Review 6.  Microglia and astrocyte dysfunction in parkinson's disease.

Authors:  Tae-In Kam; Jared T Hinkle; Ted M Dawson; Valina L Dawson
Journal:  Neurobiol Dis       Date:  2020-07-28       Impact factor: 5.996

7.  Phagocytic glia are obligatory intermediates in transmission of mutant huntingtin aggregates across neuronal synapses.

Authors:  Kirby M Donnelly; Olivia R DeLorenzo; Aprem DA Zaya; Gabrielle E Pisano; Wint M Thu; Liqun Luo; Ron R Kopito; Margaret M Panning Pearce
Journal:  Elife       Date:  2020-05-28       Impact factor: 8.140

Review 8.  Glial neuroimmune signaling in opioid reward.

Authors:  Hong Zhang; Tally M Largent-Milnes; Todd W Vanderah
Journal:  Brain Res Bull       Date:  2019-11-29       Impact factor: 4.077

Review 9.  Diversity and Function of Glial Cell Types in Multiple Sclerosis.

Authors:  Lucas Schirmer; Dorothy P Schafer; Theresa Bartels; David H Rowitch; Peter A Calabresi
Journal:  Trends Immunol       Date:  2021-02-13       Impact factor: 16.687

Review 10.  Small molecule therapeutics for neuroinflammation-mediated neurodegenerative disorders.

Authors:  Silke Miller; Maria-Jesus Blanco
Journal:  RSC Med Chem       Date:  2021-04-13
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.