4.7 Article Proceedings Paper

Microstructural imaging of human neocortex in vivo

Journal

NEUROIMAGE
Volume 182, Issue -, Pages 184-206

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2018.02.055

Keywords

hMRI; Quantitative; High resolution; Gray matter

Funding

  1. European Research Council under the European Union's Seventh Framework Programme (FP7/2007-2013) / ERC [616905]
  2. NISCI project - European Union's Horizon 2020 research and innovation programme [681094]
  3. Swiss State Secretariat for Education, Research and Innovation (SERI) [15.0137]
  4. BRAINTRAIN European research network (Collaborative Project) - European Commission [602186]
  5. BMBF [01EW1711A, 01EW1711B]
  6. European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant [658589]
  7. Deutsche Forschungsgemeinschaft [MO 2397/4-1]
  8. Marie Curie Actions (MSCA) [658589] Funding Source: Marie Curie Actions (MSCA)

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The neocortex of the human brain is the seat of higher brain function. Modern imaging techniques, chief among them magnetic resonance imaging (MRI), allow non-invasive imaging of this important structure. Knowledge of the microstructure of the neocortex has classically come from post-mortem histological studies of human tissue, and extrapolations from invasive animal studies. From these studies, we know that the scale of important neocortical structure spans six orders of magnitude, ranging from the size of axonal diameters (microns), to the size of cortical areas responsible for integrating sensory information (centimetres). MRI presents an opportunity to move beyond classical methods, because MRI is non-invasive and MRI contrast is sensitive to neocortical microstructure over all these length scales. MRI thus allows inferences to be made about neocortical microstructure in vivo, i.e. MRI-based in vivo histology. We review recent literature that has applied and developed MRI-based in vivo histology to probe the microstructure of the human neocortex, focusing specifically on myelin, iron, and neuronal fibre mapping. We find that applications such as cortical parcellation (using R-1 maps as proxies for myelin content) and investigation of cortical iron deposition with age (using R-2* maps) are already contributing to the frontiers of knowledge in neuroscience. Neuronal fibre mapping in the cortex remains challenging in vivo, but recent improvements in diffusion MRI hold promise for exciting applications in the near future. The literature also suggests that utilising multiple complementary quantitative MRI maps could increase the specificity of inferences about neocortical microstructure relative to contemporary techniques, but that further investment in modelling is required to appropriately combine the maps. In vivo histology of human neocortical microstructure is undergoing rapid development. Future developments will improve its specificity, sensitivity, and clinical applicability, granting an ever greater ability to investigate neuroscientific and clinical questions about the human neocortex.

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