Microbiome-microglia connections via the gut-brain axis

被引:394
作者
Abdel-Haq, Reem [1 ]
Schlachetzki, Johannes C. M. [2 ]
Glass, Christopher K. [2 ]
Mazmanian, Sarkis K. [1 ]
机构
[1] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
CHAIN FATTY-ACIDS; INTESTINAL BACTERIAL OVERGROWTH; ADULT HIPPOCAMPAL NEUROGENESIS; SYNUCLEIN ACTIVATES MICROGLIA; MULTIPLE-SCLEROSIS PATIENTS; PARKINSONS-DISEASE; VAGUS NERVE; ALZHEIMERS-DISEASE; TRANSCRIPTOMIC ANALYSIS; SUBSTANTIA-NIGRA;
D O I
10.1084/jem.20180794
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Microglia, the resident immune cells in the brain, are essential for modulating neurogenesis, influencing synaptic remodeling, and regulating neuroinflammation by surveying the brain microenvironment. Microglial dysfunction has been implicated in the onset and progression of several neurodevelopmental and neurodegenerative diseases; however, the multitude of factors and signals influencing microglial activity have not been fully elucidated. Microglia not only respond to local signals within the brain but also receive input from the periphery, including the gastrointestinal (GI) tract. Recent preclinical findings suggest that the gut microbiome plays a pivotal role in regulating microglial maturation and function, and altered microbial community composition has been reported in neurological disorders with known microglial involvement in humans. Collectively, these findings suggest that bidirectional crosstalk between the gut and the brain may influence disease pathogenesis. Herein, we discuss recent studies showing a role for the gut microbiome in modulating microglial development and function in homeostatic and disease conditions and highlight possible future research to develop novel microbial treatments for disorders of the brain.
引用
收藏
页码:41 / 59
页数:19
相关论文
共 211 条
[1]
MICROGLIAL RESPONSE TO 6-HYDROXYDOPAMINE-INDUCED SUBSTANTIA NIGRA LESIONS [J].
AKIYAMA, H ;
MCGEER, PL .
BRAIN RESEARCH, 1989, 489 (02) :247-253
[2]
Gut microbiota, tight junction protein expression, intestinal resistance, bacterial translocation and mortality following cholestasis depend on the genetic background of the host [J].
Alaish, Samuel M. ;
Smith, Alexis D. ;
Timmons, Jennifer ;
Greenspon, Jose ;
Eyvazzadeh, Daniel ;
Murphy, Ebony ;
Shea-Donahue, Terez ;
Cirimotich, Shana ;
Mongodin, Emmanuel ;
Zhao, Aiping ;
Fasano, Alessio ;
Nataro, James P. ;
Cross, Alan .
GUT MICROBES, 2013, 4 (04) :292-305
[3]
Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain [J].
Alliot, F ;
Godin, I ;
Pessac, B .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 117 (02) :145-152
[4]
Coupled Proliferation and Apoptosis Maintain the Rapid Turnover of Microglia in the Adult Brain [J].
Askew, Katharine ;
Li, Kaizhen ;
Olmos-Alonso, Adrian ;
Garcia-Moreno, Fernando ;
Liang, Yajie ;
Richardson, Philippa ;
Tipton, Tom ;
Chapman, Mark A. ;
Riecken, Kristoffer ;
Beccari, Sol ;
Sierra, Amanda ;
Molnar, Zoltan ;
Cragg, Mark S. ;
Garaschuk, Olga ;
Perry, V. Hugh ;
Gomez-Nicola, Diego .
CELL REPORTS, 2017, 18 (02) :391-405
[5]
The gut microbiota as an environmental factor that regulates fat storage [J].
Bäckhed, F ;
Ding, H ;
Wang, T ;
Hooper, LV ;
Koh, GY ;
Nagy, A ;
Semenkovich, CF ;
Gordon, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (44) :15718-15723
[6]
Exposure to a social stressor alters the structure of the intestinal microbiota: Implications for stressor-induced immunomodulation [J].
Bailey, Michael T. ;
Dowd, Scot E. ;
Galley, Jeffrey D. ;
Hufnagle, Amy R. ;
Allen, Rebecca G. ;
Lyte, Mark .
BRAIN BEHAVIOR AND IMMUNITY, 2011, 25 (03) :397-407
[7]
Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis [J].
Beers, David R. ;
Henkel, Jenny S. ;
Xiao, Qin ;
Zhao, Weihua ;
Wang, Jinghong ;
Yen, Albert A. ;
Siklos, Laszlo ;
McKercher, Scott R. ;
Appel, Stanley H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (43) :16021-16026
[8]
Early and Persistent Expression of Phosphorylated α-Synuclein in the Enteric Nervous System of A53T Mutant Human α-Synuclein Transgenic Mice [J].
Bencsik, Anna ;
Muselli, Letizia ;
Leboidre, Mikael ;
Lakhdar, Latifa ;
Baron, Thierry .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2014, 73 (12) :1144-1151
[9]
New tools for studying microglia in the mouse and human CNS [J].
Bennett, Mariko L. ;
Bennett, F. Chris ;
Liddelow, Shane A. ;
Ajami, Bahareh ;
Zamanian, Jennifer L. ;
Fernhoff, Nathaniel B. ;
Mulinyawe, Sara B. ;
Bohlen, Christopher J. ;
Adil, Aykezar ;
Tucker, Andrew ;
Weissman, Irving L. ;
Chang, Edward F. ;
Li, Gordon ;
Grant, Gerald A. ;
Gephart, Melanie G. Hayden ;
Barres, Ben A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (12) :E1738-E1746
[10]
Impact of consuming a milk drink containing a probiotic on mood and cognition [J].
Benton, D. ;
Williams, C. ;
Brown, A. .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2007, 61 (03) :355-361