Publications by authors named "Misaki Niu"

We recently reported that a neuronal population in the claustrum (CLA) identified under exposure to psychological stressors plays a key role in stress response processing. Upon stress exposure, the main inputs to the CLA come from the basolateral amygdala (BLA); however, the upstream brain regions that potentially regulate both the CLA and BLA during stressful experiences remain unclear. Here by combining activity-dependent viral retrograde labeling with whole brain imaging, we analyzed neurons projecting to the CLA and BLA activated by exposure to social defeat stress.

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Article Synopsis
  • The study investigates the role of the claustrum (CLA) in managing stress and anxiety, revealing it as a key area for brain communication during stress responses.
  • Researchers used advanced techniques like brain activation mapping and machine learning to show that CLA activation consistently indicates exposure to stress.
  • The findings suggest that manipulating CLA activity can influence anxiety behaviors, with silencing the CLA during stress enhancing resilience against chronic stress effects.
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  • The dopamine system is crucial for various brain functions, including motor control, and blocking its receptors can lead to significant motor disorders like catalepsy and Parkinsonism.
  • This study uses genetically modified mice to investigate brain activation patterns when exposed to two different dopamine receptor antagonists, SCH39166 and raclopride, which induce cataleptic behavior.
  • Findings reveal that specific brain areas, particularly the orbital cortex and striatum, show altered connectivity that may explain the motor dysfunctions caused by these drugs, suggesting a common underlying mechanism but with distinct connectivity changes for each drug.
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Here, we describe an optimized and detailed protocol for block-face serial microscopy tomography (FAST). FAST enables high-speed serial section fluorescence imaging of fixed brains at an axonal spatial resolution and subsequent image data processing. It renders brain-wide anatomical and functional analyses, including structural profiling of nuclear-stained brain at the single-cell level, cell-type-specific mapping with reporter animal brains and neuronal tracing with anterograde/retrograde labeling.

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Subcellular resolution imaging of the whole brain and subsequent image analysis are prerequisites for understanding anatomical and functional brain networks. Here, we have developed a very high-speed serial-sectioning imaging system named FAST (block-face serial microscopy tomography), which acquires high-resolution images of a whole mouse brain in a speed range comparable to that of light-sheet fluorescence microscopy. FAST enables complete visualization of the brain at a resolution sufficient to resolve all cells and their subcellular structures.

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MicroRNAs (miRNAs) participate in a variety of functions in the brain. Understanding the localization of miRNAs is an important step for uncovering their roles in brain function. However, the detection of low-abundance miRNAs in brain tissues remains difficult and requires extensive optimization of hybridization (ISH) protocols in individual laboratories.

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