Trem2 expression in microglia is required to maintain normal neuronal bioenergetics during development

特雷姆2 小胶质细胞 生物 海马结构 生物能学 线粒体 细胞生物学 神经科学 受体 氧化磷酸化 免疫学 炎症 遗传学 生物化学
作者
Erica Tagliatti,Genni Desiato,Sara Mancinelli,Matteo Bizzotto,Maria Cristina Gagliani,Elisa Faggiani,Rebeca Hernández‐Soto,Andrea Cugurra,Paola Poliseno,Matteo Miotto,Rafael J. Argüello,Fabia Filipello,Katia Cortese,Raffaella Morini,Simona Lodato,Michela Matteoli
出处
期刊:Immunity [Cell Press]
卷期号:57 (1): 86-105.e9 被引量:70
标识
DOI:10.1016/j.immuni.2023.12.002
摘要

Triggering receptor expressed on myeloid cells 2 (Trem2) is a myeloid cell-specific gene expressed in brain microglia, with variants that are associated with neurodegenerative diseases, including Alzheimer's disease. Trem2 is essential for microglia-mediated synaptic refinement, but whether Trem2 contributes to shaping neuronal development remains unclear. Here, we demonstrate that Trem2 plays a key role in controlling the bioenergetic profile of pyramidal neurons during development. In the absence of Trem2, developing neurons in the hippocampal cornus ammonis (CA)1 but not in CA3 subfield displayed compromised energetic metabolism, accompanied by reduced mitochondrial mass and abnormal organelle ultrastructure. This was paralleled by the transcriptional rearrangement of hippocampal pyramidal neurons at birth, with a pervasive alteration of metabolic, oxidative phosphorylation, and mitochondrial gene signatures, accompanied by a delay in the maturation of CA1 neurons. Our results unveil a role of Trem2 in controlling neuronal development by regulating the metabolic fitness of neurons in a region-specific manner.
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