Search arXivSearch

arXiv · 2112.03817

Multidimensional diffusion MRI methods with confined subdomains

Abstract

Diffusion Magnetic Resonance Imaging (dMRI) is an imaging technique with exquisite sensitivity to the microstructural properties of heterogeneous media. The conventionally adopted acquisition schemes involving single pulsed field gradients encode the random motion of water molecules into the NMR signal, however typically conflating the effects of different sources contributing to the water motion. Time-varying magnetic field gradients have recently been considered for disentangling such effects during the data encoding phase, opening to the possibility of adding specificity to the recovered information about the medium's microstructure. Such data is typically represented via a diffusion tensor distribution (DTD) model, thus assuming the existence of several non-exchanging compartments in each of which diffusion is unrestricted. In this work, we consider a model that takes confinement into account and possesses a diffusion time-dependence closer to that of restricted diffusion, to replace the free diffusion assumption in multidimensional diffusion MRI methods. We first demonstrate how the confinement tensor model captures the relevant signal modulations impressed by water diffusing in both free and closed spaces, for data simulated with a clinically feasible protocol involving time-varying magnetic field gradients. Then, we provide the basis for incorporating this model into two multidimensional dMRI methods, and attempt to recover a confinement tensor distribution (CTD) on a human brain dataset.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Deneb Boito, Cem Yolcu, Evren Özarslan. 2022-02-01. Multidimensional diffusion MRI methods with confined subdomains. https://doi.org/10.3389/fphy.2022.830274

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Signature of mechanically induced cell extrusions in cell size distribution

How a growing tissue organizes its own homeostatic state is a central question in the physics of living matter. We show that when a growing epithelial sheet counteracts increasing cell density by mechanically squeezing cells out of its plane, a homeostatic in-plane pressure emerges as a generalization of a yield stress. We find that in the quasistatic growth limit the homeostatic state is marginally stable, with a pseudogap in the distribution of local distances to the extrusion threshold pressure. Because such mechanically induced extrusions arise from an instability of individual cells, the pseudogap is imprinted in the distribution of cell areas. This provides an image-based way to test for presence of mechanically induced extrusions and we identify this signature in the developing wing epithelium of \textit{D.~melanogaster}. We expect the same principles to apply to confined three-dimensional tissues.

physics.bio-ph

Fluidization in Growth-Induced Morphogenesis

Elastic buckling has explained shape formation in growing tissues, yet the role of tissue fluidity remains elusive. We derive a minimal fluidized growth-elasticity model as a nonlinear analogue of Maxwell rheology. Analysis of a growing strip reveals a different picture of growth-induced morphogenesis: rather than emerging at a critical stress, symmetry breaking develops continuously during growth. Fluidity regulates stress evolution, the rate of shape-symmetry breaking, and flow patterns, establishing it as an active regulator of morphogenesis beyond its intuitive role in stress relaxation.

physics.bio-ph

The Motile-Units model: Interacting spins model of cell polarization and motility

We introduce a coarse-grained interacting-spin model for two-dimensional cell motility, in which the cell perimeter is discretized into stochastic binary spins that switch between active and inactive states. Each perimeter spin represents a "motile-unit" that is a source of protrusive force and retrograde flow when active. Long-range interactions between the motile-units arise through a polarity cue advected by the collective actin retrograde flow, providing a minimal realization of spontaneous symmetry breaking and self-propulsion. The model exhibits three dynamical phases, a random walk phase, persistent random walk phase, and an intermittent bistable phase characterized by run-and-tumble migration. Additional nearest-neighbor interactions modulate speed and persistence without altering the overall phase structure. Owing to its simplicity, the framework naturally incorporates external cues, reproducing chemotactic migration, steering by localized optogenetic activation, and directional decision-making (symmetry breaking) under competing stimuli. The model introduces a new class of active-particle model in which both speed and polarity emerge from internal stochastic spin dynamics, rather than being imposed as particle-level variables, offering a framework for the study of cell migration and extends the scope of active-matter physics.

physics.bio-ph