Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/99831
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Type: Journal article
Title: Systematic review of the neurobiological relevance of chemokines to psychiatric disorders
Author: Stuart, M.
Singhal, G.
Baune, B.
Citation: Frontiers in Cellular Neuroscience, 2015; 9(September):357-1-357-15
Publisher: Frontiers
Issue Date: 2015
ISSN: 1662-5102
1662-5102
Statement of
Responsibility: 
Michael J. Stuart, Gaurav Singhal, and Bernhard T. Baune
Abstract: Psychiatric disorders are highly prevalent and disabling conditions of increasing public health relevance. Much recent research has focused on the role of cytokines in the pathophysiology of psychiatric disorders; however, the related family of immune proteins designated chemokines has been relatively neglected. Chemokines were originally identified as having chemotactic function on immune cells; however, recent evidence has begun to elucidate novel, brain-specific functions of these proteins of relevance to the mechanisms of psychiatric disorders. A systematic review of both human and animal literature in the PubMed and Google Scholar databases was undertaken. After application of all inclusion and exclusion criteria, 157 references were remained for the review. Some early mechanistic evidence does associate select chemokines with the neurobiological processes, including neurogenesis, modulation of the neuroinflammatory response, regulation of the hypothalamus-pituitary-adrenal axis, and modulation of neurotransmitter systems. This early evidence however does not clearly demonstrate any specificity for a certain psychiatric disorder, but is primarily relevant to mechanisms which are shared across disorders. Notable exceptions include CCL11 that has recently been shown to impair hippocampal function in aging - of distinct relevance to Alzheimer's disease and depression in the elderly, and pre-natal exposure to CXCL8 that may disrupt early neurodevelopmental periods predisposing to schizophrenia. Pro-inflammatory chemokines, such as CCL2, CCL7, CCL8, CCL12, and CCL13, have been shown to drive chemotaxis of pro-inflammatory cells to the inflamed or injured CNS. Likewise, CX3CL has been implicated in promoting glial cells activation, pro-inflammatory cytokines secretion, expression of ICAM-1, and recruitment of CD4+ T-cells into the CNS during neuroinflammatory processes. With further translational research, chemokines may present novel diagnostic and/or therapeutic targets in psychiatric disorders.
Keywords: Depression
Alzheimer’s disease
neurogenesis
chemokine
schizophrenia
inflammation
immune
neurodegeneration
Rights: © 2015 Stuart, Singhal and Baune. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
DOI: 10.3389/fncel.2015.00357
Grant ID: http://purl.org/au-research/grants/nhmrc/1043771
Published version: http://dx.doi.org/10.3389/fncel.2015.00357
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