Manganese‐enhanced magnetic resonance imaging (MEMRI) of mouse brain development

Given the importance of genetically modified mice in studies of mammalian brain development and human congenital brain diseases, MRI has the potential to provide an efficient in vivo approach for analyzing mutant phenotypes in the early postnatal mouse brain. The combination of reduced tissue contrast at the high magnetic fields required for mice, and the changing cellular composition of the developing mouse brain make it difficult to optimize MRI contrast in neonatal mouse imaging. We have explored an easily implemented approach for contrast‐enhanced imaging, using systemically administered manganese (Mn) to reveal fine anatomical detail in T1‐weighted MR images of neonatal mouse brains. In particular, we demonstrate the utility of this Mn‐enhanced MRI (MEMRI) method for analyzing early postnatal patterning of the mouse cerebellum. Through comparisons with matched histological sections, we further show that MEMRI enhancement correlates qualitatively with granule cell density in the developing cerebellum, suggesting that the cerebellar enhancement is due to uptake of Mn in the granule neurons. Finally, variable cerebellar defects in mice with a conditional mutation in the Gbx2 gene were analyzed with MEMRI to demonstrate the utility of this method for mutant mouse phenotyping. Taken together, our results indicate that MEMRI provides an efficient and powerful in vivo method for analyzing neonatal brain development in normal and genetically engineered mice. Copyright © 2004 John Wiley & Sons, Ltd.

[1]  David G Norris,et al.  High field human imaging , 2003, Journal of magnetic resonance imaging : JMRI.

[2]  Hao Huang,et al.  Three-dimensional anatomical characterization of the developing mouse brain by diffusion tensor microimaging , 2003, NeuroImage.

[3]  R. Buist,et al.  Periventricular/Intraventricular Hemorrhage in Neonatal Mouse Cerebrum , 2003, Journal of neuropathology and experimental neurology.

[4]  D. Turnbull,et al.  Mn-Enhanced MRI of Neural Activity in the mouse Midbrain , 2003 .

[5]  Hiroto Hatabu,et al.  MR imaging at high magnetic fields. , 2003, European journal of radiology.

[6]  A. Shukakidze,et al.  Behavioral Impairments in Acute and Chronic Manganese Poisoning in White Rats , 2003, Neuroscience and Behavioral Physiology.

[7]  S. Neubauer,et al.  High‐resolution imaging of normal anatomy, and neural and adrenal malformations in mouse embryos using magnetic resonance microscopy , 2003, Journal of anatomy.

[8]  Daniel H Turnbull,et al.  Induction of medulloblastomas in mice by sonic hedgehog, independent of Gli1. , 2002, Cancer research.

[9]  Jens Frahm,et al.  In vivo 3D MRI staining of mouse brain after subcutaneous application of MnCl2 , 2002, Magnetic resonance in medicine.

[10]  A. Joyner,et al.  Changing Requirements for Gbx2 in Development of the Cerebellum and Maintenance of the Mid/Hindbrain Organizer , 2002, Neuron.

[11]  B. Fredholm,et al.  MRI Evaluation and Functional Assessment of Brain Injury After Hypoxic Ischemia in Neonatal Mice , 2002, Stroke.

[12]  S. Sourbron,et al.  Study of pediatric brain development using magnetic resonance imaging of anisotropic diffusion. , 2002, Magnetic resonance imaging.

[13]  M. Solaiyappan,et al.  Diffusion tensor imaging of the developing mouse brain , 2001, Magnetic resonance in medicine.

[14]  Richard T. Miller,et al.  Neurotoxicity of manganese chloride in neonatal and adult CD rats following subchronic (21‐day) high‐dose oral exposure , 2000, Journal of applied toxicology : JAT.

[15]  J. Rademacher,et al.  Measuringin VivoMyelination of Human White Matter Fiber Tracts with Magnetization Transfer MR , 1999, NeuroImage.

[16]  R. Ashikaga,et al.  Appearance of normal brain maturation on fluid-attenuated inversion-recovery (FLAIR) MR images. , 1999, AJNR. American journal of neuroradiology.

[17]  R E Jacobs,et al.  Looking deeper into vertebrate development. , 1999, Trends in cell biology.

[18]  Afonso C. Silva,et al.  In vivo neuronal tract tracing using manganese‐enhanced magnetic resonance imaging , 1998, Magnetic resonance in medicine.

[19]  A. Snyder,et al.  Normal brain in human newborns: apparent diffusion coefficient and diffusion anisotropy measured by using diffusion tensor MR imaging. , 1998, Radiology.

[20]  A. Koretsky,et al.  Manganese ion enhances T1‐weighted MRI during brain activation: An approach to direct imaging of brain function , 1997, Magnetic resonance in medicine.

[21]  G. Johnson,et al.  Magnetic resonance microscopy of mouse embryos. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[22]  A. Joyner,et al.  Abnormal embryonic cerebellar development and patterning of postnatal foliation in two mouse Engrailed-2 mutants. , 1994, Development.

[23]  T. Seki,et al.  Magnetic resonance signal intensity ratio of gray/white matter in children Quantitative assessment in developing brain , 1993, Brain and Development.

[24]  Robert E. London,et al.  Magnetic resonance imaging studies of the brains of anesthetized rats treated with manganese chloride , 1989, Brain Research Bulletin.

[25]  J. Valk,et al.  MR imaging of the various stages of normal myelination during the first year of life , 2004, Neuroradiology.

[26]  R E Jacobs,et al.  Towards a microMRI atlas of mouse development. , 1999, Computerized medical imaging and graphics : the official journal of the Computerized Medical Imaging Society.