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Donzanti, M. J.

Publications and source records attributed to Donzanti, M. J..

3 recordsLinked to original sources

Anatomical 3D Reconstruction of Murine Lymph Nodes for Visualization, Quantitation, and Numerical Simulation

Lymph nodes (LNs) function as pharmacological sanctuary sites in HIV and metastatic cancer due to anatomical barriers that limit drug penetration. Accurate 3D reconstructions of lymph node architecture are essential for computational modeling of drug transport, yet existing methods lack compartment-specific resolution, accessibility, or throughput. Here, we present a scalable, high-fidelity pipeline for the 3D anatomical reconstruction of murine LNs, integrating optimized vibratome sectioning, multiplexed immunofluorescence staining, confocal microscopy, and custom automated segmentation algorithms. Our method precisely reconstructs key LN compartments, including lobules and high endothelial venules, with high spatial accuracy, achieving Sorensen-Dice indices >0.93 for lobules and contour-matching scores up to 77% for vasculature, as validated by quantitative comparison to manual segmentation. Compared to existing methodologies, this pipeline markedly reduces reagent usage ([~] 88%), labor time ([~] 97%), and technical complexity, offering a broadly accessible and efficient approach to high-fidelity 3D anatomical reconstruction of LN architecture. These digital twins can support computational simulations of drug distribution, immune cell trafficking, and spatial pharmacokinetics, providing critical insights into LN-resident disease mechanisms and informing therapeutic design.

bioengineering↗

Confocal-Compatible Workflow for Sectioning, Staining, and Imaging Serial Vibratome Sections for 3D Anatomical Reconstruction of the Lymph Node

3D anatomical reconstruction provides quantitative insight into tissue architecture, variability, and function. However, existing whole-organ imaging methods, such as light-sheet microscopy and micro-CT, are often costly, slow, and inaccessible for many laboratories. We present an accessible, confocal-compatible workflow for harvesting, sectioning, and staining murine lymph nodes for high-fidelity 3D reconstruction. The protocol preserves Z-plane resolution through vibratome sectioning and immunostaining, enabling detailed visualization of lymph node lobules and vasculature using standard confocal microscopes. The resulting image stacks can be used for quantitative morphometry and spatiotemporal pharmacokinetic modeling. This reproducible workflow expands access to spatial and structural studies of the lymph node and can be adapted to other small, heterogeneous organs. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=50 SRC="FIGDIR/small/685350v1_ufig1.gif" ALT="Figure 1"> View larger version (17K): org.highwire.dtl.DTLVardef@1e16022org.highwire.dtl.DTLVardef@16e6366org.highwire.dtl.DTLVardef@3ffee6org.highwire.dtl.DTLVardef@177c2af_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗

Stochastic to Deterministic: A straightforward approach to create serially perfusable multiscale capillary beds

Generation of in vitro tissue models with serially perfused hierarchical vasculature would allow greater control of fluid perfusion throughout the network and enable direct mechanistic investigation of vasculogenesis, angiogenesis, and vascular remodeling. In this work, we have developed a method to produce a closed, serially perfused, multiscale vessel network embedded within an acellular hydrogel. We confirmed that the acellular and cellular gel-gel interface was functionally annealed without preventing or biasing cell migration and endothelial self-assembly. Multiscale connectivity of the vessel network was validated via high-resolution microscopy techniques to confirm anastomosis between self-assembled and patterned vessels. Lastly, using fluorescently labeled microspheres, the multiscale network was serially perfused to confirm patency and barrier function. Directional flow from inlet to outlet man-dated flow through the capillary bed. This method for producing closed, multiscale vascular networks was developed with the intention of straightforward fabrication and engineering techniques so as to be a low barrier to entry for researchers who wish to investigate mechanistic questions in vascular biology. This ease of use offers a facile extension of these methods for incorporation into organoid culture, organ-on-a-chip (OOC) models, and bioprinted tissues.

bioengineering↗