{"title":"Red Blood Cell Dynamics in Healthy and Cancer-Influenced Venular Flow: Role of Flow Conditions and Cell Stiffness.","authors":"Tahereh Zarei, Cyrus Aghanajafi, M Soltani","doi":"10.1159/jvr/adiag007","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hemodynamic alterations in microvessels under pathological conditions such as cancer can modify RBC dynamics and near-wall behavior, influencing the cell-free layer and local flow microenvironment.</p><p><strong>Methods: </strong>Three-dimensional simulations of two red blood cells with different stiffness levels were performed in venular flow under conditions representing a healthy individual and a breast cancer patient. The simulations were carried out using a force-coupling immersed-boundary lattice Boltzmann framework. RBC deformation, longitudinal and radial migration, velocity distribution, shear rate, and pressure fields were analyzed using hematocrit data, with blood viscosity derived from these data.</p><p><strong>Results: </strong>Compared with healthy flow, cancer-affected conditions led to reduced RBC deformation and diminished radial migration, resulting in increased near-wall residence. This effect was more pronounced for the stiffened RBC. It was accompanied by a local reduction in near-wall velocity, an increase in shear rate, and larger pressure differences across the cell. Shear rate was higher in cancer-affected flow, while near-wall variations were reduced.</p><p><strong>Conclusions: </strong>The results indicate that cancer-associated changes in venular flow promote RBC near-wall localization and may suppress CFL formation, primarily due to reduced RBC deformation, overriding low-hematocrit dilution. Circulating tumor cells were not modeled; however, RBC dynamics suggest a microenvironment that may facilitate near-wall interactions.</p>","PeriodicalId":17530,"journal":{"name":"Journal of Vascular Research","volume":" ","pages":"1"},"PeriodicalIF":1.3000,"publicationDate":"2026-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Vascular Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1159/jvr/adiag007","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Hemodynamic alterations in microvessels under pathological conditions such as cancer can modify RBC dynamics and near-wall behavior, influencing the cell-free layer and local flow microenvironment.
Methods: Three-dimensional simulations of two red blood cells with different stiffness levels were performed in venular flow under conditions representing a healthy individual and a breast cancer patient. The simulations were carried out using a force-coupling immersed-boundary lattice Boltzmann framework. RBC deformation, longitudinal and radial migration, velocity distribution, shear rate, and pressure fields were analyzed using hematocrit data, with blood viscosity derived from these data.
Results: Compared with healthy flow, cancer-affected conditions led to reduced RBC deformation and diminished radial migration, resulting in increased near-wall residence. This effect was more pronounced for the stiffened RBC. It was accompanied by a local reduction in near-wall velocity, an increase in shear rate, and larger pressure differences across the cell. Shear rate was higher in cancer-affected flow, while near-wall variations were reduced.
Conclusions: The results indicate that cancer-associated changes in venular flow promote RBC near-wall localization and may suppress CFL formation, primarily due to reduced RBC deformation, overriding low-hematocrit dilution. Circulating tumor cells were not modeled; however, RBC dynamics suggest a microenvironment that may facilitate near-wall interactions.
期刊介绍:
The ''Journal of Vascular Research'' publishes original articles and reviews of scientific excellence in vascular and microvascular biology, physiology and pathophysiology. The scope of the journal covers a broad spectrum of vascular and lymphatic research, including vascular structure, vascular function, haemodynamics, mechanics, cell signalling, intercellular communication, growth and differentiation. JVR''s ''Vascular Update'' series regularly presents state-of-the-art reviews on hot topics in vascular biology. Manuscript processing times are, consistent with stringent review, kept as short as possible due to electronic submission. All articles are published online first, ensuring rapid publication. The ''Journal of Vascular Research'' is the official journal of the European Society for Microcirculation. A biennial prize is awarded to the authors of the best paper published in the journal over the previous two years, thus encouraging young scientists working in the exciting field of vascular biology to publish their findings.