4.7 Article

Macrophage Transcriptional Profile Identifies Lipid Catabolic Pathways That Can Be Therapeutically Targeted after Spinal Cord Injury

期刊

JOURNAL OF NEUROSCIENCE
卷 37, 期 9, 页码 2362-2376

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2751-16.2017

关键词

axon regeneration; fibrotic scar; foamy macrophages; glial scar; myelin laden macrophages; neuroinflammation

资金

  1. NINDS [R01NS081040, R21NS082835, R01HD057632]
  2. U.S. Army Grant [W81XWH131007715]
  3. Miami Project to Cure Paralysis
  4. Buoniconti Fund
  5. Walter G. Ross Foundation

向作者/读者索取更多资源

Although infiltrating macrophages influence many pathological processes after spinal cord injury (SCI), the intrinsic molecular mechanisms that regulate their function are poorly understood. A major hurdle has been dissecting macrophage-specific functions from those in other cell types as well as understanding how their functions change over time. Therefore, we used the RiboTag method to obtain macrophage-specific mRNA directly from the injured spinal cord in mice and performed RNA sequencing to investigate their transcriptional profile. Our data show that at 7 d after SCI, macrophages are best described as foam cells, with lipid catabolism representing the main biological process, and canonical nuclear receptor pathways as their potential mediators. Genetic deletion of a lipoprotein receptor, CD36, reduces macrophage lipid content and improves lesion size and locomotor recovery. Therefore, we report the first macrophage-specific transcriptional profile after SCI and highlight the lipid catabolic pathway as an important macrophage function that can be therapeutically targeted after SCI.

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