A spatio-temporal brain miRNA expression atlas identifies sex-independent age-related microglial driven miR-155-5p increase.

时空脑 miRNA 表达图谱揭示了与性别无关的年龄相关性小胶质细胞驱动的 miR-155-5p 增加

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作者:Engel Annika, Wagner Viktoria, Hahn Oliver, Foltz Aulden G, Atkins Micaiah, Beganovic Amila, Guldner Ian H, Lu Nannan, Saksena Aryaman, Fischer Ulrike, Ludwig Nicole, Meese Eckart, Wyss-Coray Tony, Keller Andreas
An in-depth understanding of the molecular processes composing aging is crucial to develop therapeutic approaches that decrease aging as a key risk factor for cognitive decline. Herein, we present a spatio-temporal brain atlas (15 different regions) of microRNA expression across the mouse lifespan (7 time points) and two aging interventions. MicroRNAs are promising therapeutic targets, as they silence genes by complementary base-pair binding of messenger RNAs and mediate aging speed. We first established sex- and brain-region-specific microRNA expression patterns in young adult samples. Then we focused on sex-dependent and independent brain-region-specific microRNA expression changes during aging. We identified three sex-independent brain aging microRNAs (miR-146a-5p, miR-155-5p, and miR-5100). For miR-155-5p, we showed that these expression changes are driven by aging microglia and target mTOR signaling pathway components and other cellular communication pathways. In this work, we identify strong sex-brain-region-specific aging microRNAs and microglial miR-155-5p as a promising therapeutic target.

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