Brain region- and sex-specific transcriptional profiles of microglia

被引:22
作者
Barko, Kelly [1 ]
Shelton, Micah [1 ]
Xue, Xiangning [2 ]
Afriyie-Agyemang, Yvette [1 ,3 ]
Puig, Stephanie [4 ,5 ]
Freyberg, Zachary [1 ,3 ,6 ]
Tseng, George C. [2 ]
Logan, Ryan W. [4 ,5 ,7 ]
Seney, Marianne L. [1 ,3 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Psychiat, Translat Neurosci Program, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Sch Publ Hlth, Dept Biostat, Pittsburgh, PA USA
[3] Univ Pittsburgh, Ctr Neurosci, Pittsburgh, PA 15260 USA
[4] Boston Univ, Sch Med, Dept Pharmacol & Expt Therapeut, Boston, MA USA
[5] Boston Univ, Ctr Syst Neurosci, Boston, MA USA
[6] Univ Pittsburgh, Dept Cell Biol, Pittsburgh, PA USA
[7] Boston Univ, Sch Med, Genome Sci Inst, Boston, MA USA
来源
FRONTIERS IN PSYCHIATRY | 2022年 / 13卷
关键词
microglia; RNA-sequencing; Tmem119; disease-associated microglia; sex difference; GENE-EXPRESSION; SELENOPROTEIN W; MOUSE-BRAIN; ER-ALPHA; ADULT; ACTIVATION; REVEALS; BINDING; RAT; POLYMORPHISMS;
D O I
10.3389/fpsyt.2022.945548
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Microglia are resident macrophages of the brain, performing roles related to brain homeostasis, including modulation of synapses, trophic support, phagocytosis of apoptotic cells and debris, as well as brain protection and repair. Studies assessing morphological and transcriptional features of microglia found regional differences as well as sex differences in some investigated brain regions. However, markers used to isolate microglia in many previous studies are not expressed exclusively by microglia or cannot be used to identify and isolate microglia in all contexts. Here, fluorescent activated cell sorting was used to isolate cells expressing the microglia-specific marker TMEM119 from prefrontal cortex (PFC), striatum, and midbrain in mice. RNA-sequencing was used to assess the transcriptional profile of microglia, focusing on brain region and sex differences. We found striking brain region differences in microglia-specific transcript expression. Most notable was the distinct transcriptional profile of midbrain microglia, with enrichment for pathways related to immune function; these midbrain microglia exhibited a profile similar to disease-associated or immune-surveillant microglia. Transcripts more highly expressed in PFC isolated microglia were enriched for synapse-related pathways while microglia isolated from the striatum were enriched for pathways related to microtubule polymerization. We also found evidence for a gradient of expression of microglia-specific transcripts across the rostral-to-caudal axes of the brain, with microglia extracted from the striatum exhibiting a transcriptional profile intermediate between that of the PFC and midbrain. We also found sex differences in expression of microglia-specific transcripts in all 3 brain regions, with many selenium-related transcripts more highly expressed in females across brain regions. These results suggest that the transcriptional profile of microglia varies between brain regions under homeostatic conditions, suggesting that microglia perform diverse roles in different brain regions and even based on sex.
引用
收藏
页数:17
相关论文
共 94 条
  • [1] Local self-renewal can sustain CNS microglia maintenance and function throughout adult life
    Ajami, Bahareh
    Bennett, Jami L.
    Krieger, Charles
    Tetzlaff, Wolfram
    Rossi, Fabio M. V.
    [J]. NATURE NEUROSCIENCE, 2007, 10 (12) : 1538 - 1543
  • [2] New tools for studying microglia in the mouse and human CNS
    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.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (12) : E1738 - E1746
  • [3] Human microglia regional heterogeneity and phenotypes determined by multiplexed single-cell mass cytometry
    Boettcher, Chotima
    Schlickeiser, Stephan
    Sneeboer, Marjolein A. M.
    Kunkel, Desiree
    Knop, Anniki
    Paza, Evdokia
    Fidzinski, Pawel
    Kraus, Larissa
    Snijders, Gijsje J. L.
    Kahn, Rene S.
    Schulz, Axel R.
    Mei, Henrik E.
    Hol, Elly M.
    Siegmund, Britta
    Glauben, Rainer
    Spruth, Eike J.
    de Witte, Lot D.
    Priller, Josef
    [J]. NATURE NEUROSCIENCE, 2019, 22 (01) : 78 - +
  • [4] Differential effects of stress on microglial cell activation in male and female medial prefrontal cortex
    Bollinger, Justin L.
    Burns, Christine M. Bergeon
    Wellman, Cara L.
    [J]. BRAIN BEHAVIOR AND IMMUNITY, 2016, 52 : 88 - 97
  • [5] Effects of selective estrogen receptor modulators (SERMs) on coactivator nuclear receptor (NR) box binding to estrogen receptors
    Bramlett, KS
    Burris, TP
    [J]. MOLECULAR GENETICS AND METABOLISM, 2002, 76 (03) : 225 - 233
  • [6] Tissue-specific functions of individual glutathione peroxidases
    Brigelius-Flohé, R
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (9-10) : 951 - 965
  • [7] Genetic Cell Ablation Reveals Clusters of Local Self-Renewing Microglia in the Mammalian Central Nervous System
    Bruttger, Julia
    Karram, Khalad
    Woertge, Simone
    Regen, Tommy
    Marini, Federico
    Hoppmann, Nicola
    Klein, Matthias
    Blank, Thomas
    Yona, Simon
    Wolf, Yochai
    Mack, Matthias
    Pinteaux, Emmanuel
    Mueller, Werner
    Zipp, Frauke
    Binder, Harald
    Bopp, Tobias
    Prinz, Marco
    Jung, Steffen
    Waisman, Ari
    [J]. IMMUNITY, 2015, 43 (01) : 92 - 106
  • [8] Sall1 is a transcriptional regulator defining microglia identity and function
    Buttgereit, Anne
    Lelios, Iva
    Yu, Xueyang
    Vrohlings, Melissa
    Krakoski, Natalie R.
    Gautier, Emmanuel L.
    Nishinakamura, Ryuichi
    Becher, Burkhard
    Greter, Melanie
    [J]. NATURE IMMUNOLOGY, 2016, 17 (12) : 1397 - 1406
  • [9] Improved identification of concordant and discordant gene expression signatures using an updated rank-rank hypergeometric overlap approach
    Cahill, Kelly M.
    Huo, Zhiguang
    Tseng, George C.
    Logan, Ryan W.
    Seney, Marianne L.
    [J]. SCIENTIFIC REPORTS, 2018, 8
  • [10] Blocking the Thiol at Cysteine-322 Destabilizes Tau Protein and Prevents Its Oligomer Formation
    Chen, Hui
    Liu, Simu
    Li, Shuiming
    Chen, Jierui
    Ni, Jiazuan
    Liu, Qiong
    [J]. ACS CHEMICAL NEUROSCIENCE, 2018, 9 (07): : 1560 - 1565