Mohammed Bendaoud,Alexis Darras,Yazdan Rashidi,Christian Wagner,Chaouqi Misbah
{"title":"Red Blood Cell Positional History, Sphericity, and Network Architecture Influence Lingering and Partitioning","authors":"Mohammed Bendaoud,Alexis Darras,Yazdan Rashidi,Christian Wagner,Chaouqi Misbah","doi":"10.1016/j.bpj.2026.09.024","DOIUrl":null,"url":null,"abstract":"The transport and distribution of red blood cells (RBCs) through microvascular networks is central to diverse applications in drug delivery, tissue engineering, and the study of pathological mechanisms. Recent findings highlight two critical phenomena: (i) a history-dependent partitioning effect, wherein the RBC partitioning at each bifurcation is influenced by the positional and configurational state inherited from previous bifurcations and (ii) RBC lingering at the bifurcation apex, which strongly affects downstream flow distribution. However, the interplay between network geometry, RBC sphericity (in spherocytosis disease), and these emergent behaviors remains insufficiently explored. Here, we perform two-dimensional Lattice Boltzmann simulations coupled with an immersed boundary model to systematically investigate RBC dynamics in both asymmetric and fully symmetric network designs. Our results show that RBC positional history grows progressively with each bifurcation, leading to increasing deviations from classical partitioning laws regardless of the network’s geometric complexity. We further demonstrate that even spherical RBCs can experience substantial lingering due to cumulative apex interactions, challenging the notion that only elongated or pathologically deformed cells are prone to these effects. These findings clarify how RBC deformability and prior apex encounters affect microcirculatory flow.","PeriodicalId":8922,"journal":{"name":"Biophysical journal","volume":"32 1","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2026-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysical journal","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.bpj.2026.09.024","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
The transport and distribution of red blood cells (RBCs) through microvascular networks is central to diverse applications in drug delivery, tissue engineering, and the study of pathological mechanisms. Recent findings highlight two critical phenomena: (i) a history-dependent partitioning effect, wherein the RBC partitioning at each bifurcation is influenced by the positional and configurational state inherited from previous bifurcations and (ii) RBC lingering at the bifurcation apex, which strongly affects downstream flow distribution. However, the interplay between network geometry, RBC sphericity (in spherocytosis disease), and these emergent behaviors remains insufficiently explored. Here, we perform two-dimensional Lattice Boltzmann simulations coupled with an immersed boundary model to systematically investigate RBC dynamics in both asymmetric and fully symmetric network designs. Our results show that RBC positional history grows progressively with each bifurcation, leading to increasing deviations from classical partitioning laws regardless of the network’s geometric complexity. We further demonstrate that even spherical RBCs can experience substantial lingering due to cumulative apex interactions, challenging the notion that only elongated or pathologically deformed cells are prone to these effects. These findings clarify how RBC deformability and prior apex encounters affect microcirculatory flow.
期刊介绍:
BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.