4.7 Article

In vivo imaging of inhibitory, GABAergic neurons by MRI

期刊

NEUROIMAGE
卷 62, 期 3, 页码 1685-1693

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2012.05.029

关键词

Responsive MRI contrast agent; Stem cell differentiation protocol for GABAergic neurons; Glutamic acid decarboxylase; In vivo MRI of GABAergic neurons

资金

  1. ENCITE EU-FP7 [HEALTH-F5-2008-201842]
  2. Volkswagen Foundation [1/83 443]
  3. region Piemonte (PIIMDMT project)
  4. region Piemonte (Nano-IGT project)
  5. Italian Consortium CIRCMSB
  6. EC-FP6 [MC-IRG-013080]
  7. KU Leuven [PF 10/017 IMIR]

向作者/读者索取更多资源

The unambiguous detection of specific neuronal subtypes is up to now only possible with invasive techniques or optical imaging after genetic modification. High field magnetic resonance imaging (MRI) has the ability to visualize the brain structure and anatomy noninvasively, with high resolution - but missing the cell specific and functional information. Here we present a new tool for neuroimaging with MRI, enabling the selective detection of GABAergic neurons under in vivo conditions. The specific imaging contrast is achieved by a novel paramagnetic contrast agent, which responds to the activity of the enzyme glutamic acid decarboxylase - expressed solely by inhibitory neurons. The relaxivity of the complex is increased upon decarboxylation of two glutamic acid moieties, thus allowing increased water access to the inner and outer coordination spheres of the paramagnetic ion. The mechanism and specificity of activation were proven with tissue lysates and further applied to a differentiation protocol for murine embryonic stem cells. The relaxation enhancement was studied quantitatively and revealed decreased longitudinal relaxation times in the inhibitory neuron samples compared to the naive stem cells in vitro and in vivo. Furthermore, this approach offers not only the discrimination of inhibitory, GABAergic neurons in the brain but also may expand the usefulness of MRI for functional imaging on a cellular level. (c) 2012 Elsevier Inc. All rights reserved.

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