4.8 Article

Neuronal activity increases translocator protein (TSPO) levels

期刊

MOLECULAR PSYCHIATRY
卷 26, 期 6, 页码 2025-2037

出版社

SPRINGERNATURE
DOI: 10.1038/s41380-020-0745-1

关键词

-

资金

  1. Swiss National Science Foundation [310030_188524, PZ00P3_18009/1]
  2. Medical Research Council [MR/L010305/1]
  3. Forschungskredit from the University of Zurich
  4. Jane Hodge Foundation, UK
  5. [P2ZHP3_174868]
  6. Swiss National Science Foundation (SNF) [310030_188524] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

The study found that neuronal activity can modify TSPO levels in the adult central nervous system. TSPO gene and protein are widely expressed in the hippocampus, but their levels increase only in neurons after stimulating neuronal activity, rather than in glial cells.
The mitochondrial protein, translocator protein (TSPO), is a widely used biomarker of neuroinflammation, but its non-selective cellular expression pattern implies roles beyond inflammatory processes. In the present study, we investigated whether neuronal activity modifies TSPO levels in the adult central nervous system. First, we used single-cell RNA sequencing to generate a cellular landscape of basal TSPO gene expression in the hippocampus of adult (12 weeks old) C57BL6/N mice, followed by confocal laser scanning microscopy to verify TSPO protein in neuronal and non-neuronal cell populations. We then quantified TSPO mRNA and protein levels after stimulating neuronal activity with distinct stimuli, including designer receptors exclusively activated by designer drugs (DREADDs), exposure to a novel environment and acute treatment with the psychostimulant drug, amphetamine. Single-cell RNA sequencing demonstrated a non-selective and multi-cellular gene expression pattern of TSPO at basal conditions in the adult mouse hippocampus. Confocal laser scanning microscopy confirmed that TSPO protein is present in neuronal and non-neuronal (astrocytes, microglia, vascular endothelial cells) cells of cortical (medial prefrontal cortex) and subcortical (hippocampus) brain regions. Stimulating neuronal activity through chemogenetic (DREADDs), physiological (novel environment exposure) or psychopharmacological (amphetamine treatment) approaches led to consistent increases in TSPO gene and protein levels in neurons, but not in microglia or astrocytes. Taken together, our findings show that neuronal activity has the potential to modify TSPO levels in the adult central nervous system. These findings challenge the general assumption that altered TSPO expression or binding unequivocally mirrors ongoing neuroinflammation and emphasize the need to consider non-inflammatory interpretations in some physiological or pathological contexts.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据