Abstract

The red blood cell has become implicated in the progression of a range of diseases; mechanisms by which red cells are involved appear to include the transport of inflammatory species via red cell-derived vesicles. We review this role of RBCs in diseases such as diabetes mellitus, sickle cell anemia, polycythemia vera, central retinal vein occlusion, Gaucher disease, atherosclerosis, and myeloproliferative neoplasms. We propose a possibly unifying, and novel, paradigm for the inducement of RBC vesiculation during vascular flow of red cells adhered to the vascular endothelium as well as to the red pulp of the spleen. Indeed, we review the evidence for this hypothesis that links physiological conditions favoring both vesiculation and enhanced RBC adhesion and demonstrate the veracity of this hypothesis by way of a specific example occurring in splenic flow which we argue has various renderings in a wide range of vascular flows, in particular microvascular flows. We provide a mechanistic basis for membrane loss and the formation of lysed red blood cells in the spleen that may mediate their turnover. Our detailed explanation for this example also makes clear what features of red cell deformability are involved in the vesiculation process and hence require quantification and a new form of quantitative indexing.

Highlights

  • Their model scenario was closely tailored to the videomicroscopy observations of MacDonald et al [89] as illustrated by the snapshots shown in Figure 1d; the imposed flow was, calibrated to match that directly recorded in the videos

  • We review and summarize the essential findings so that they may provide veracity for our hypothesis as well as point to the biophysical mechanisms that lead to membrane loss, vesiculation, and hemolysis of adhered red cells

  • We note that the contact pressure reaches levels of O(∼125 Pa) which is sufficient in itself to induce skeleton-membrane decohesion [88], independent of what is caused by skeleton-membrane disruption due to e.g., oxidative damage as assessed by Zhu et al [98]; when such localized M↔S damage, i.e., de-cohered regions, exist tether formation and vesiculation are strongly favored [44]

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Summary

Introduction

The role of enhanced red cell adhesion to the vascular endothelium has been implicated as an element of the process by which vesicles are released [18,19,20,21,22,23,24,25,26], and thereby in the progression of a wide range of dysfunctions; these include, inter alia, polycythemia vera [12,18,19,20,21]; central retinal vein occlusion [27,28,29]; Gaucher disease [26,30]; myeloproliferative neoplasms [31]; atherosclerosis [1,2,4]; sickle cell disease [32,33,34,35]; and diabetes mellitus [11,36,37] This range of disease states suggests that some unifying principles may exist. Erythrocyte slit passage has been simulated using a hierarchal multiscale molecular-continuum model [69,74,98]

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