scholarly journals PHYSICOCHEMICAL EFFECTS OF ALDEHYDES ON THE HUMAN ERYTHROCYTE

1972 ◽  
Vol 53 (3) ◽  
pp. 809-818 ◽  
Author(s):  
P. S. Vassar ◽  
J. M. Hards ◽  
D. E. Brooks ◽  
B. Hagenberger ◽  
G. V. F. Seaman
Keyword(s):  
Red Blood Cells ◽  
Blood Cells ◽  
Negative Charge ◽  
The Other ◽  
Red Cell ◽  
Volume Changes ◽  
Cell Deformability ◽  
Red Cell Deformability ◽  
Human Red Blood Cells ◽  
Formaldehyde Treatment

The effects of formaldehyde, acetaldehyde, and glutaraldehyde on human red blood cells were investigated. It was found that (a) The surface negative charge of the erythrocytes at pH 7 was increased 10% by glutaraldehyde, but not by the other two aldehydes. (b) The effect of incomplete fixation of the red blood cells was demonstrated by hemoglobin leakage studies The leakage of hemoglobin subsequent to formaldehyde treatment was especially pronounced Acetaldehyde-fixed cells showed some leakage of hemoglobin after an hour of exposure to the fixative, whereas glutaraldehyde-fixed cells showed no hemoglobin leakage. (c) All three aldehydes caused K+ leakage during fixation. The concentrations of K+ in the fixing solutions all reached the same level, but whereas the leakage with glutaraldehyde was immediate, that with formaldehyde was more gradual and that with acetaldehyde reached a steady state only after 24 hr. (d) The effects of the aldehydes on red cell deformability and swelling revealed that glutaraldehyde hardened the cells within 15 min, formaldehyde within 5 hr, while acetaldehyde required at least 24 hr to produce appreciable fixation. (e) The hematocrit changes accompanying the fixation process depended upon cell volume changes and loss of deformability.

scholarly journals Red Blood Cells: Tethering, Vesiculation, and Disease in Micro-Vascular Flow

Diagnostics ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 971
Author(s):  
Robert J. Asaro ◽  
Pedro Cabrales
Keyword(s):  
Red Blood Cells ◽  
Blood Cells ◽  
Myeloproliferative Neoplasms ◽  
Red Cells ◽  
Red Cell ◽  
Cell Deformability ◽  
Red Cell Deformability ◽  
Vascular Flow ◽  
Wide Range ◽  
Mechanistic Basis

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.

scholarly journals How Do Red Blood Cells Die?

2021 ◽  
Vol 12 ◽  
Author(s):  
Perumal Thiagarajan ◽  
Charles J. Parker ◽  
Josef T. Prchal
Keyword(s):  
Red Blood Cells ◽  
Blood Cells ◽  
Red Cells ◽  
Cell Labeling ◽  
Red Cell ◽  
Average Life Span ◽  
Human Red Blood Cells ◽  
Physicochemical Changes ◽  
Cell Clearance

Normal human red blood cells have an average life span of about 120 days in the circulation after which they are engulfed by macrophages. This is an extremely efficient process as macrophages phagocytose about 5 million erythrocytes every second without any significant release of hemoglobin in the circulation. Despite large number of investigations, the precise molecular mechanism by which macrophages recognize senescent red blood cells for clearance remains elusive. Red cells undergo several physicochemical changes as they age in the circulation. Several of these changes have been proposed as a recognition tag for macrophages. Most prevalent hypotheses for red cell clearance mechanism(s) are expression of neoantigens on red cell surface, exposure phosphatidylserine and decreased deformability. While there is some correlation between these changes with aging their causal role for red cell clearance has not been established. Despite plethora of investigations, we still have incomplete understanding of the molecular details of red cell clearance. In this review, we have reviewed the recent data on clearance of senescent red cells. We anticipate recent progresses in in vivo red cell labeling and the explosion of modern proteomic techniques will, in near future, facilitate our understanding of red cell senescence and their destruction.

scholarly journals Comparative rheology of human and trout red blood cells.

1993 ◽  
Vol 174 (1) ◽  
pp. 109-122
Author(s):  
G B Nash ◽  
S Egginton
Keyword(s):  
Red Blood Cells ◽  
Blood Cells ◽  
Applied Pressure ◽  
Blood Rheology ◽  
Tissue Perfusion ◽  
Red Cells ◽  
Cell Deformability ◽  
Red Cell Deformability ◽  
Rainbow Trout Oncorhynchus Mykiss ◽  
Circulatory Parameter

We have studied the comparative rheology of individual red blood cells from humans and rainbow trout (Oncorhynchus mykiss) at their natural body temperatures. Trout red blood cells were large ellipsoids (about 16 microns x 11.5 microns x 2.5 microns) with a mean volume of 250 fl, a surface area of approximately 350 microns 2 and an elongated nucleus of about 9 microns x 5 microns. Although much larger than human red cells (diameter 8 microns, V = 92 fl, A = 136 microns 2), both theoretical calculation and experimental aspiration into micropipettes indicated that the limiting size of a cylindrical vessel that both types of cell could enter was approximately 3 microns. Nevertheless, individual trout red cells had much longer transit times through 5 microns filter pores and were much slower to enter 3-4 microns diameter micropipettes. Interestingly, the relative deformability of the trout cells depended on the pore size and applied pressure, with entry times for trout and human cells converging as pipette diameter increased. The relatively poor overall cellular deformability of the trout cells reflected their membrane rigidity (shear elastic modulus 4-5 times higher than that of human membrane), as well as their large size and the presence of a prominent nucleus. Capillary diameters in trout muscle are similar to those in the human microcirculation (about 3 microns), while systemic driving pressures are much lower. Therefore, either red cell deformability is a less critical circulatory parameter than has previously been thought, or the apparently disadvantageous blood rheology of trout is adequate because of the lower demand for tissue perfusion.

scholarly journals Red blood cell size is important for adherence of blood platelets to artery subendothelium

Blood ◽  
1983 ◽  
Vol 62 (1) ◽  
pp. 214-217 ◽  
Author(s):  
PA Aarts ◽  
PA Bolhuis ◽  
KS Sakariassen ◽  
RM Heethaar ◽  
JJ Sixma
Keyword(s):  
Red Blood Cells ◽  
Cell Size ◽  
Blood Cells ◽  
Blood Platelets ◽  
Red Cells ◽  
Cell Diameter ◽  
Red Cell ◽  
Human Red Blood Cells ◽  
Platelet Adherence ◽  
Order Of Magnitude

Abstract The hematocrit is one of the main factors influencing platelet adherence to the vessel wall. Raising the hematocrit causes an increase of platelet accumulation of about an order of magnitude. Our studies concern the role of red cell size. We have studied this effect using an annular perfusion chamber, according to Baumgartner, with human umbilical arteries and a steady-flow system. Normal human red blood cells (MCV 95 cu mu) increased platelet adherence sevenfold, as the hematocrit increases from 0 to 0.6. Small erythrocytes from goats (MCV 25 cu mu) caused no increment in adherence in the same hematocrit range. Rabbit erythrocytes (MCV 70 cu mu) caused an intermediate increase in adherence. Red blood cells from newborns (MCV 110–130 cu mu) caused a larger increase in platelet adherence than normal red cells at hematocrit 0.4. These results were further confirmed with large red blood cells from two patients. Experiments with small red cells (MCV 70 cu mu) of patients with iron deficiency showed that platelet adherence was similar to normal red cells, provided the red cell diameter was normal. Small red blood cells of a patient with sideroblastic anemia caused decreased adherence. These data indicate that red cell size is of major importance for platelet adherence. Red cell diameter is more important than average volume. However, for size differences in the human range, the hematocrit remains the dominant parameter.

scholarly journals Blood group D antigen content of nucleated red cell precursors

Blood ◽  
1977 ◽  
Vol 50 (6) ◽  
pp. 981-986 ◽  
Author(s):  
A Rearden ◽  
SP Masouredis
Keyword(s):  
Bone Marrow ◽  
Red Blood Cells ◽  
Blood Group ◽  
Blood Cells ◽  
Cell Types ◽  
The Other ◽  
Cell Maturation ◽  
Red Cell ◽  
D Antigen ◽  
Group D

Abstract The D antigen content of nucleated red cell precursors in human bone marrow was estimated using autoradiography and 125I-anti-D. D antigen first appeared in the pronormoblast, and the quantity of antigen progressively increased during red cell maturation. Maximal anti-D binding occurred on mature red blood cells. Pronormoblasts, basophilic normoblasts, polychromatophilic normoblasts, and orthochromatic normoblasts, respectively, had approximately 1/4, 1/2, 2/3, and 3/4 the quantity of antigen found on mature red cells. None of the other cell types were found in bone marrow labeled with anti-D.

scholarly journals Red blood cell size is important for adherence of blood platelets to artery subendothelium

Blood ◽  
1983 ◽  
Vol 62 (1) ◽  
pp. 214-217 ◽  
Author(s):  
PA Aarts ◽  
PA Bolhuis ◽  
KS Sakariassen ◽  
RM Heethaar ◽  
JJ Sixma
Keyword(s):  
Red Blood Cells ◽  
Cell Size ◽  
Blood Cells ◽  
Blood Platelets ◽  
Red Cells ◽  
Cell Diameter ◽  
Red Cell ◽  
Human Red Blood Cells ◽  
Platelet Adherence ◽  
Order Of Magnitude

The hematocrit is one of the main factors influencing platelet adherence to the vessel wall. Raising the hematocrit causes an increase of platelet accumulation of about an order of magnitude. Our studies concern the role of red cell size. We have studied this effect using an annular perfusion chamber, according to Baumgartner, with human umbilical arteries and a steady-flow system. Normal human red blood cells (MCV 95 cu mu) increased platelet adherence sevenfold, as the hematocrit increases from 0 to 0.6. Small erythrocytes from goats (MCV 25 cu mu) caused no increment in adherence in the same hematocrit range. Rabbit erythrocytes (MCV 70 cu mu) caused an intermediate increase in adherence. Red blood cells from newborns (MCV 110–130 cu mu) caused a larger increase in platelet adherence than normal red cells at hematocrit 0.4. These results were further confirmed with large red blood cells from two patients. Experiments with small red cells (MCV 70 cu mu) of patients with iron deficiency showed that platelet adherence was similar to normal red cells, provided the red cell diameter was normal. Small red blood cells of a patient with sideroblastic anemia caused decreased adherence. These data indicate that red cell size is of major importance for platelet adherence. Red cell diameter is more important than average volume. However, for size differences in the human range, the hematocrit remains the dominant parameter.

scholarly journals Deformability of Stored Red Blood Cells

2021 ◽  
Vol 12 ◽  
Author(s):  
Gregory Barshtein ◽  
Ivana Pajic-Lijakovic ◽  
Alexander Gural
Keyword(s):  
Red Blood Cells ◽  
Cold Storage ◽  
Blood Cells ◽  
Storage Conditions ◽  
Cell Deformability ◽  
Red Cell Deformability ◽  
Peripheral Tissues ◽  
Pass Through

Red blood cells (RBCs) deformability refers to the cells’ ability to adapt their shape to the dynamically changing flow conditions so as to minimize their resistance to flow. The high red cell deformability enables it to pass through small blood vessels and significantly determines erythrocyte survival. Under normal physiological states, the RBCs are attuned to allow for adequate blood flow. However, rigid erythrocytes can disrupt the perfusion of peripheral tissues and directly block microvessels. Therefore, RBC deformability has been recognized as a sensitive indicator of RBC functionality. The loss of deformability, which a change in the cell shape can cause, modification of cell membrane or a shift in cytosol composition, can occur due to various pathological conditions or as a part of normal RBC aging (in vitro or in vivo). However, despite extensive research, we still do not fully understand the processes leading to increased cell rigidity under cold storage conditions in a blood bank (in vitro aging), In the present review, we discuss publications that examined the effect of RBCs’ cold storage on their deformability and the biological mechanisms governing this change. We first discuss the change in the deformability of cells during their cold storage. After that, we consider storage-related alterations in RBCs features, which can lead to impaired cell deformation. Finally, we attempt to trace a causal relationship between the observed phenomena and offer recommendations for improving the functionality of stored cells.

scholarly journals Ionic and osmotic equilibria of human red blood cells treated with nystatin.

1979 ◽  
Vol 74 (2) ◽  
pp. 157-185 ◽  
Author(s):  
J C Freedman ◽  
J F Hoffman
Keyword(s):  
Red Blood Cells ◽  
Cell Volume ◽  
Blood Cells ◽  
Osmotic Coefficients ◽  
Virial Equation ◽  
Red Cell ◽  
Extracellular Solution ◽  
Red Cell Volume ◽  
Human Red Blood Cells ◽  
Cell Volumes

Human red blood cells have been incubated in the presence of nystatin, which allows Na and K, as well as Cl and pH to equilibrate rapidly when cell volume is set with external impermeant sucrose. The intracellular mean ionic activity coefficients, relative to values in the extracellular solution, for KCl and NaCl are 1.01 +/- 0.02 and 0.99 +/- 0.02 (SD, n = 10), respectively, and are independent of external pH, pH o, and of [sucrose]o. With nystatin the dependence of red cell volume on [sucrose]o deviates from ideal osmotic behavior by as much as a factor of three. A virial equation for the osmotic coefficient, phi, of human hemoglobin, Hb, accounts for the cell volumes, and is the same as that which describes Adair's measurements of phi Hb for Hb isolated from sheep and ox bloods. In the presence of nystatin the slope of the acid-base titration curve of the cells is independent of cell volume, implying that the charge on impermeant cellular solutes is independent of Hb concentration at constant pH. By modifying the Jacobs-stewart equations (1947. J. Cell. Comp. Physiol. 30: 79--103) with the osmotic coefficients of Hb and of salts, a nonideal thermodynamic model has been devised which predicts equilibrium Donnan ratios and red cell volume from the composition of the extracellular solution and from certain parameters of the cells. In addition to accounting for the dependence of cell volume on osmotic pressure, the model also describes accurately the dependence of Donnan ratios and cell volumes on pHo either in the presence or absence of nystatin.

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