Evidence map›Paper›PMID 39990367›Full record

ArticlebioRxiv : the preprint server for biology2025

Three-dimensional modeling of flow through microvascular beds and surrounding interstitial spaces.

Navaneeth Krishna Rajeeva Pandian, Alanna Farell, Emily Davis, Subramanian Sundaram, Abraham Christoffel Ignatius van Steen, Jessica Li Chang Teo, Jeroen Eyckmans, Christopher S Chen

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Navaneeth Krishna Rajeeva PandianHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Alanna FarellHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Emily DavisHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Subramanian SundaramHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Abraham Christoffel Ignatius van SteenHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Jessica Li Chang TeoHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Jeroen EyckmansHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.
Christopher S ChenHarvard Wyss Institute for Biologically Inspired Engineering, Boston, MA 02115, USA.

Funding

Synthetic vascularization and regeneration in engineered tissuesR01EB033821 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SANGEETA N. BHATIA, CHRISTOPHER S CHEN · 2023 to 2026
$2.2M
NIBIB NIH HHS R01 EB033821Wellcome Trust
6 · The paper itself

Abstract

The health and function of microvascular beds are dramatically impacted by the mechanical forces that they experience due to fluid flow. These fluid flow-generated forces are challenging to measure directly and are typically calculated from experimental flow data. However, current computational fluid dynamics (CFD) models either employ truncated 2D models or overlook the presence of extraluminal flows within the interstitial space between vessels that result from the permeability of the endothelium lining the vessels, which are crucial components affecting flow dynamics. To address this, we present a bottom-up modeling approach that assesses fluid flow in 3D-engineered vessel networks featuring an endothelial lining and interstitial space. Using image processing algorithms to segment 3D confocal image stacks from engineered capillary networks, we reconstructed a 3D computational model of the networks. We incorporated vascular permeability and matrix porosity values to model the contributions of the endothelial lining and interstitial spaces to the flow dynamics in the networks. Simulations suggest that including the endothelial monolayer and the interstitium significantly affects the predicted flow magnitude in the vessels and flow profiles in the interstitium. To demonstrate the importance of these factors, we showed experimentally and computationally that while cytokine (IL-1β) treatment did not affect the network architecture, it significantly increased vessel permeability and resulted in a dramatic decrease in wall shear stresses and flow velocities intraluminally within the networks. In conclusion, this framework offers a robust methodology for studying flow dynamics in 3D in vitro vessel networks, enhancing our understanding of vascular physiology and pathology.

Identifiers

PMID39990367
PMCPMC11844386

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.