A sensorimotor-association axis of thalamocortical connection development
Valerie J. SydnoriD, Joëlle BagautdinovaiD, Bart LarseniD, Michael J. ArcaroiD, Deanna M. BarchiD, Dani S. BassettiD, Aaron F. Alexander‐BlochiD, Philip A. CookiD, Sydney C. CovitziD, Alexandre R. FrancoiD, Raquel E. GuriD, Ruben C. GuriD, Allyson P. MackeyiD, Kahini P. MehtaiD, Steven L. MeisleriD, Michael Peter MilhamiD, Tyler M. MooreiD, Eli J. MülleriD, David R. RoalfiD, Taylor SaloiD, Gabriel Schubiner, Jakob SeidlitziD, Russell Taki ShinoharaiD, James M. ShineiD, Fang-Cheng F. YehiD, , Theodore Daniel SatterthwaiteiD
Abstract
Human cortical development follows a sensorimotor-to-association sequence during childhood and adolescence1-6. The brains capacity to enact this sequence over decades indicates that it relies on intrinsic mechanisms to regulate inter-regional differences in the timing of cortical maturation, yet regulators of human developmental chronology are not well understood. Given evidence from animal models that thalamic axons modulate windows of cortical plasticity7-12, here we evaluate the overarching hypothesis that structural connections between the thalamus and cortex help to coordinate cortical maturational heterochronicity during youth. We first introduce, cortically annotate, and anatomically validate a new atlas of human thalamocortical connections using diffusion tractography. By applying this atlas to three independent youth datasets (ages 8-23 years; total N = 2,676), we reproducibly demonstrate that thalamocortical connections develop along a maturational gradient that aligns with the cortexs sensorimotor-association axis. Associative cortical regions with thalamic connections that take longest to mature exhibit protracted expression of neurochemical, structural, and functional markers indicative of higher circuit plasticity as well as heightened environmental sensitivity. This work highlights a central role for the thalamus in the orchestration of hierarchically organized and environmentally sensitive windows of cortical developmental malleability.
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