TY - JOUR
T1 - Spatiotemporal tissue maturation of thalamocortical pathways in the human fetal brain
AU - Wilson, Sian
AU - Pietsch, Maximilian
AU - Cordero-Grande, Lucilio
AU - Christiaens, Daan
AU - Uus, Alena
AU - Karolis, Vyacheslav R
AU - Kyriakopoulou, Vanessa
AU - Colford, Kathleen
AU - Price, Anthony N
AU - Hutter, Jana
AU - Rutherford, Mary A
AU - Hughes, Emer J
AU - Counsell, Serena J
AU - Tournier, Jacques-Donald
AU - Hajnal, Joseph V
AU - Edwards, A David
AU - O'Muicheartaigh, Jonathan
AU - Arichi, Tomoki
N1 - Funding Information:
We thank the patients who agreed to participate in this work and the staff of St Thomas’ Hospital London. This work was supported by the European Research Council under the European Union Seventh Framework Programme (FP/2007–2013)/ERC Grant Agreement No. 319456. We acknowledge infrastructure support from the National Institute for Health Research (NIHR) Mental Health Biomedical Research Centre (BRC) at South London and Maudsley NHS Foundation Trust, King’s College London, and the NIHR-BRC at Guy’s and St Thomas’ NHS Foundation Trust. We also acknowl-edge grant support in part from the Wellcome Engineering and Physical Sciences Research Council (EPSRC) Centre for Medical Engineering at King’s College London (WT 203148/Z/16/Z) and the Medical Research Council (UK) (MR/K006355/1) and (MR/L011530/1). SW was supported by PhD funding from the UK Medical Research Council/Sackler Foundation (MR/P502108/1). JO is supported by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (206675/Z/17/Z). JO, MR, ADE, JO, and TA received support from the Medical Research Council Centre for Neurodevelopmental Disorders, King’s College London (MR/N026063/1). TA was supported by an MRC Clinician Scientist Fellowship (MR/P008712/1). VK and TA were supported by an MRC Transition Support Award (MR/V036874/1). Support for this work was also provided by the NIHR-BRC at Kings College London, Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London, and King’s College Hospital NHS Foundation Trust.
Funding Information:
We thank the patients who agreed to participate in this work and the staff of St Thomas’ Hospital London. This work was supported by the European Research Council under the European Union Seventh Framework Programme (FP/2007–2013)/ERC Grant Agreement No. 319456. We acknowledge infrastructure support from the National Institute for Health Research (NIHR) Mental Health Biomedical Research Centre (BRC) at South London and Maudsley NHS Foundation Trust, King’s College London, and the NIHR-BRC at Guy’s and St Thomas’ NHS Foundation Trust. We also acknowledge grant support in part from the Wellcome Engineering and Physical Sciences Research Council (EPSRC) Centre for Medical Engineering at King’s College London (WT 203148/Z/16/Z) and the Medical Research Council (UK) (MR/K006355/1) and (MR/L011530/1). SW was supported by PhD funding from the UK Medical Research Council/Sackler Foundation (MR/P502108/1). JO is supported by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (206675/Z/17/Z). JO, MR, ADE, JO, and TA received support from the Medical Research Council Centre for Neurodevel-opmental Disorders, King’s College London (MR/N026063/1). TA was supported by an MRC Clinician Scientist Fellowship (MR/P008712/1). VK and TA were supported by an MRC Transition Support Award (MR/V036874/1). Support for this work was also provided by the NIHR-BRC at Kings College London, Guy’s and St Thomas’ NHS Foundation Trust in partnership with King’s College London, and King’s College Hospital NHS Foundation Trust.
Funding Information:
Translation support fellowship: MR/V036874/1
Publisher Copyright:
© Wilson et al.
PY - 2023/4/3
Y1 - 2023/4/3
N2 - The development of connectivity between the thalamus and maturing cortex is a fundamental process in the second half of human gestation, establishing the neural circuits that are the basis for several important brain functions. In this study, we acquired high-resolution in utero diffusion magnetic resonance imaging (MRI) from 140 fetuses as part of the Developing Human Connectome Project, to examine the emergence of thalamocortical white matter over the second to third trimester. We delineate developing thalamocortical pathways and parcellate the fetal thalamus according to its cortical connectivity using diffusion tractography. We then quantify microstructural tissue components along the tracts in fetal compartments that are critical substrates for white matter maturation, such as the subplate and intermediate zone. We identify patterns of change in the diffusion metrics that reflect critical neurobiological transitions occurring in the second to third trimester, such as the disassembly of radial glial scaffolding and the lamination of the cortical plate. These maturational trajectories of MR signal in transient fetal compartments provide a normative reference to complement histological knowledge, facilitating future studies to establish how developmental disruptions in these regions contribute to pathophysiology.
AB - The development of connectivity between the thalamus and maturing cortex is a fundamental process in the second half of human gestation, establishing the neural circuits that are the basis for several important brain functions. In this study, we acquired high-resolution in utero diffusion magnetic resonance imaging (MRI) from 140 fetuses as part of the Developing Human Connectome Project, to examine the emergence of thalamocortical white matter over the second to third trimester. We delineate developing thalamocortical pathways and parcellate the fetal thalamus according to its cortical connectivity using diffusion tractography. We then quantify microstructural tissue components along the tracts in fetal compartments that are critical substrates for white matter maturation, such as the subplate and intermediate zone. We identify patterns of change in the diffusion metrics that reflect critical neurobiological transitions occurring in the second to third trimester, such as the disassembly of radial glial scaffolding and the lamination of the cortical plate. These maturational trajectories of MR signal in transient fetal compartments provide a normative reference to complement histological knowledge, facilitating future studies to establish how developmental disruptions in these regions contribute to pathophysiology.
UR - http://www.scopus.com/inward/record.url?scp=85153804425&partnerID=8YFLogxK
U2 - 10.7554/eLife.83727
DO - 10.7554/eLife.83727
M3 - Article
C2 - 37010273
SN - 2050-084X
VL - 12
JO - eLife
JF - eLife
M1 - e83727
ER -