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Human-specific paralogs of SRGAP2 induce neotenic features of microglia structural and functional maturation.
Diaz-Salazar, Carlos; Krzisch, Marine; Yoo, Juyoun; Nano, Patricia R; Bhaduri, Aparna; Jaenisch, Rudolf; Polleux, Franck.
Afiliação
  • Diaz-Salazar C; Department of Neuroscience, Columbia University, New York, NY, 10027, USA.
  • Krzisch M; Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University; New York, NY, 10027, USA.
  • Yoo J; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
  • Nano PR; Department of Neuroscience, Columbia University, New York, NY, 10027, USA.
  • Bhaduri A; Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University; New York, NY, 10027, USA.
  • Jaenisch R; Department of Biological Chemistry, University of California Los Angeles, Los Angeles, CA 90095, USA.
  • Polleux F; Department of Biological Chemistry, University of California Los Angeles, Los Angeles, CA 90095, USA.
bioRxiv ; 2024 Jun 29.
Article em En | MEDLINE | ID: mdl-38979266
ABSTRACT
Microglia play key roles in shaping synaptic connectivity during neural circuits development. Whether microglia display human-specific features of structural and functional maturation is currently unknown. We show that the ancestral gene SRGAP2A and its human-specific (HS) paralogs SRGAP2B/C are not only expressed in cortical neurons but are the only HS gene duplications expressed in human microglia. Here, using combination of xenotransplantation of human induced pluripotent stem cell (hiPSC)-derived microglia and mouse genetic models, we demonstrate that (1) HS SRGAP2B/C are necessary and sufficient to induce neotenic features of microglia structural and functional maturation in a cell-autonomous manner, and (2) induction of SRGAP2-dependent neotenic features of microglia maturation non-cell autonomously impacts synaptic development in cortical pyramidal neurons. Our results reveal that, during human brain evolution, human-specific genes SRGAP2B/C coordinated the emergence of neotenic features of synaptic development by acting as genetic modifiers of both neurons and microglia.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos