4.7 Article

Cell specificity of Manganese-enhanced MRI signal in the cerebellum

Journal

NEUROIMAGE
Volume 276, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2023.120198

Keywords

Cellular resolution; Molecular imaging; Multimodal registration; Genetically engineered mouse models; Pharmacogenetic ablation

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Magnetic Resonance Imaging (MRI) resolution is improving, and understanding the cellular basis for different MRI contrast mechanisms is important. Manganese-enhanced MRI (MEMRI) can visualize cellular cytoarchitecture in the brain, especially in the cerebellum. In this study, the effects of selective ablation of Purkinje cells or Bergmann glia on cerebellar MEMRI signal were quantified, and it was found that the Purkinje cells are the primary source of signal enhancement in the Purkinje cell layer.
Magnetic Resonance Imaging (MRI) resolution continues to improve, making it important to understand the cellular basis for different MRI contrast mechanisms. Manganese-enhanced MRI (MEMRI) produces layer-specific contrast throughout the brain enabling in vivo visualization of cellular cytoarchitecture, particularly in the cerebellum. Due to the unique geometry of the cerebellum, especially near the midline, 2D MEMRI images can be acquired from a relatively thick slice by averaging through areas of uniform morphology and cytoarchitecture to produce very high-resolution visualization of sagittal planes. In such images, MEMRI hyperintensity is uniform in thickness throughout the anterior-posterior axis of sagittal sections and is centrally located in the cerebellar cortex. These signal features suggested that the Purkinje cell layer, which houses the cell bodies of the Purkinje cells and the Bergmann glia, is the source of hyperintensity. Despite this circumstantial evidence, the cellular source of MRI contrast has been difficult to define. In this study, we quantified the effects of selective ablation of Purkinje cells or Bergmann glia on cerebellar MEMRI signal to determine whether signal could be assigned to one cell type. We found that the Purkinje cells, not the Bergmann glia, are the primary of source of the enhancement in the Purkinje cell layer. This cell-ablation strategy should be useful for determining the cell specificity of other MRI contrast mechanisms.

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