Transcriptional and Translational Differences of Microglia from Male and Female Brains

被引:329
作者
Guneykaya, Dilansu [1 ]
Ivanov, Andranik [2 ,3 ]
Hernandez, Daniel Perez [4 ,5 ]
Haage, Verena [1 ]
Wojtas, Bartosz [7 ]
Meyer, Niklas [1 ]
Maricos, Meron [1 ]
Jordan, Philipp [1 ]
Buonfiglioli, Alice [1 ,6 ]
Gielniewski, Bartlomiej [7 ]
Ochocka, Natalia [7 ]
Coemert, Cagla [1 ]
Friedrich, Corinna [4 ]
Artiles, Lorena Suarez [4 ]
Kaminska, Bozena [7 ]
Mertins, Philipp [4 ,5 ]
Beule, Dieter [2 ,8 ]
Kettenmann, Helmut [1 ]
Wolf, Susanne A. [1 ,9 ]
机构
[1] Helmholtz Assoc, Max Delbrueck Ctr Mol Med, Cellular Neuroci, Berlin, Germany
[2] Berlin Inst Hlth, Core Unit Bioinformat, Berlin, Germany
[3] Charite, Berlin, Germany
[4] Helmholtz Assoc, Max Delbrueck Ctr Mol Med, Prote Platform, D-13125 Berlin, Germany
[5] Berlin Inst Hlth, D-13125 Berlin, Germany
[6] Charite, Inst Cell Biol & Neurobiol, Berlin, Germany
[7] Polish Acad Sci, Nencki Inst Expt Biol, Warsaw, Poland
[8] Helmholtz Assoc, Max Delbrueck Ctr Mol Med, Berlin, Germany
[9] Charite, Dept Ophthalmol, Augustenburger Pl 1, D-13353 Berlin, Germany
关键词
SEX-DIFFERENCES; GENE-EXPRESSION; PROTEIN; ACTIVATION; MICE; AGE; PHAGOCYTOSIS; MATURATION; SYSTEM; CELLS;
D O I
10.1016/j.celrep.2018.08.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sex differences in brain structure and function are of substantial scientific interest because of sex-related susceptibility to psychiatric and neurological disorders. Neuroinflammation is a common denominator of many of these diseases, and thus microglia, as the brain's immunocompetent cells, have come into focus in sex-specific studies. Here, we show differences in the structure, function, and transcriptomic and proteomic profiles in microglia freshly isolated from male and female mouse brains. We show that male microglia are more frequent in specific brain areas, have a higher antigen-presenting capacity, and appear to have a higher potential to respond to stimuli such as ATP, reflected in higher baseline outward and inward currents and higher protein expression of purinergic receptors. Altogether, we provide a comprehensive resource to generate and validate hypotheses regarding brain sex differences.
引用
收藏
页码:2773 / +
页数:17
相关论文
共 58 条
[1]   Global signatures of protein and mRNA expression levels [J].
Abreu, Raquel de Sousa ;
Penalva, Luiz O. ;
Marcotte, Edward M. ;
Vogel, Christine .
MOLECULAR BIOSYSTEMS, 2009, 5 (12) :1512-1526
[2]   Sex differences in glia reactivity after cortical brain injury [J].
Acaz-Fonseca, Estefania ;
Duran, Juan C. ;
Carrero, Paloma ;
Garcia-Segura, Luis M. ;
Angeles Arevalo, M. .
GLIA, 2015, 63 (11) :1966-1981
[3]  
[Anonymous], 2001, J WOMEN HEALTH GEN-B, V10, P433
[4]  
Arnold Arthur P, 2012, Handb Exp Pharmacol, P67, DOI 10.1007/978-3-642-30726-3_4
[5]   The predictive nature of transcript expression levels on protein expression in adult human brain [J].
Bauernfeind, Amy L. ;
Babbitt, Courtney C. .
BMC GENOMICS, 2017, 18
[6]   Purinergic receptors on microglial cells:: functional expression in acute brain slices and modulation of microglial activation in vitro [J].
Boucsein, C ;
Zacharias, R ;
Färber, K ;
Pavlovic, S ;
Hanisch, UK ;
Kettenmann, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 17 (11) :2267-2276
[7]   Electrophysiological properties of microglial cells in normal and pathologic rat brain slices [J].
Boucsein, C ;
Kettenmann, H ;
Nolte, C .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (06) :2049-2058
[8]   MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification [J].
Cox, Juergen ;
Mann, Matthias .
NATURE BIOTECHNOLOGY, 2008, 26 (12) :1367-1372
[9]   Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation [J].
Dewing, P ;
Shi, T ;
Horvath, S ;
Vilain, E .
MOLECULAR BRAIN RESEARCH, 2003, 118 (1-2) :82-90
[10]   STAR: ultrafast universal RNA-seq aligner [J].
Dobin, Alexander ;
Davis, Carrie A. ;
Schlesinger, Felix ;
Drenkow, Jorg ;
Zaleski, Chris ;
Jha, Sonali ;
Batut, Philippe ;
Chaisson, Mark ;
Gingeras, Thomas R. .
BIOINFORMATICS, 2013, 29 (01) :15-21