Novel Hexb-based tools for studying microglia in the CNS

Takahiro Masuda, Lukas Amann, Roman Sankowski, Ori Staszewski, Maximilian Lenz, Paolo d´Errico, Nicolas Snaidero, Marta Joana Costa Jordão, Chotima Böttcher, Katrin Kierdorf, Steffen Jung, Josef Priller, Thomas Misgeld, Andreas Vlachos, Melanie Meyer Luehmann, Klaus Peter Knobeloch, Marco Prinz

研究成果: ジャーナルへの寄稿学術誌査読

93 被引用数 (Scopus)


Microglia and central nervous system (CNS)-associated macrophages (CAMs), such as perivascular and meningeal macrophages, are implicated in virtually all diseases of the CNS. However, little is known about their cell-type-specific roles in the absence of suitable tools that would allow for functional discrimination between the ontogenetically closely related microglia and CAMs. To develop a new microglia gene targeting model, we first applied massively parallel single-cell analyses to compare microglia and CAM signatures during homeostasis and disease and identified hexosaminidase subunit beta (Hexb) as a stably expressed microglia core gene, whereas other microglia core genes were substantially downregulated during pathologies. Next, we generated HexbtdTomato mice to stably monitor microglia behavior in vivo. Finally, the Hexb locus was employed for tamoxifen-inducible Cre-mediated gene manipulation in microglia and for fate mapping of microglia but not CAMs. In sum, we provide valuable new genetic tools to specifically study microglia functions in the CNS.

ジャーナルNature Immunology
出版ステータス出版済み - 7月 1 2020

!!!All Science Journal Classification (ASJC) codes

  • 免疫アレルギー学
  • 免疫学


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