High Angular Resolution Diffusion MRI Reveals Conserved and Deviant Programs in the Paths that Guide Human Cortical Circuitry

Author:

Charvet Christine J1,Das Avilash234,Song Jae W5,Tindal-Burgess Deselyn J1,Kabaria Priya6,Dai Guangping7,Kane Tara6,Takahashi Emi348

Affiliation:

1. Department of Psychology, Delaware State University, Dover, DE 19901, USA

2. Medical Sciences in the College of Arts and Sciences, Boston University, Boston, MA 02215, USA

3. Division of Newborn Medicine, Department of Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02215, USA

4. Fetal-Neonatal Brain Imaging and Developmental Science Center, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02215, USA

5. Division of Neuroradiology, Department of Radiology, Massachusetts General Hospital, Boston, MA 02114, USA

6. Department of Behavioral Neuroscience, Northeastern University, Boston, MA 02115, USA

7. Science Center, Wellesley College, Wellesley, MA 02481, USA

8. Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA

Abstract

Abstract Diffusion magnetic resonance (MR) tractography represents a novel opportunity to investigate conserved and deviant developmental programs between humans and other species such as mice. To that end, we acquired high angular resolution diffusion MR scans of mice [embryonic day (E) 10.5 to postnatal week 4] and human brains [gestational week (GW) 17–30] at successive stages of fetal development to investigate potential evolutionary changes in radial organization and emerging pathways between humans and mice. We compare radial glial development as well as commissural development (e.g., corpus callosum), primarily because our findings can be integrated with previous work. We also compare corpus callosal growth trajectories across primates (i.e., humans and rhesus macaques) and rodents (i.e., mice). One major finding is that the developing cortex of humans is predominated by pathways likely associated with a radial glial organization at GW 17–20, which is not as evident in age-matched mice (E 16.5, 17.5). Another finding is that, early in development, the corpus callosum follows a similar developmental timetable in primates (i.e., macaques and humans) as in mice. However, the corpus callosum grows for an extended period of time in primates compared with rodents. Taken together, these findings highlight deviant developmental programs underlying the emergence of cortical pathways in the human brain.

Funder

National Institute of Neurological Disorders and Stroke

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute of Mental Health

Center for Functional Neuroimaging Technologies

National Center for Research Resources

High-End Instrumentation Grant Program

National Institute of General Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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