The area and volume of single human erythrocytes during gradual osmotic swelling to hemolysis

1970 ◽  
Vol 48 (6) ◽  
pp. 369-376 ◽  
Author(s):  
Peter B. Canham ◽  
David R. Parkinson

A double-chambered slide was designed for the microscope which would enable continuous viewing of cells hanging on edge in a Ringer solution which was gradually being reduced in osmotic pressure. This was achieved by putting a dialysis membrane between the cell chamber and a chamber containing distilled water. Photographs were taken at 1-min intervals of single cells on edge (revealing the biconcave profile) until the cells hemolyzed, usually within 30 min. The area and volume of revolution of each cell were calculated from measurements on photographic enlargements. No significant change in area occurs during the swelling series although the red cell changes gradually from biconcave to spherical and remains spherical for approximately 7 min before hemolyzing. This stability is best explained by a leakage of potassium ion from the cell prior to hemolysis (which has been reported by Seeman to be approximately 20%).

1978 ◽  
Vol 44 (2) ◽  
pp. 254-257 ◽  
Author(s):  
Y. Kakiuchi ◽  
A. B. DuBois ◽  
D. Gorenberg

Hansen's membrane manometer method for measuring plasma colloid osmotic pressure was used to obtain the osmolality changes of dogs breathing different levels of CO2. Osmotic pressure was converted to osmolality by calibration of the manometer with saline and plasma, using freezing point depression osmometry. The addition of 10 vol% of CO2 to tonometered blood caused about a 2.0 mosmol/kg H2O increase of osmolality, or 1.2% increase of red blood cell volume. The swelling of the red blood cells was probably due to osmosis caused by Cl- exchanged for the HCO3- which was produced rapidly by carbonic anhydrase present in the red blood cells. The change in colloid osmotic pressure accompanying a change in co2 tension was measured on blood obtained from dogs breathing different CO2 mixtures. It was approximately 0.14 mosmol/kg H2O per Torr Pco2. The corresponding change in red cell volume could not be calculated from this because water can exchange between the plasma and tissues.


1920 ◽  
Vol 2 (3) ◽  
pp. 273-296 ◽  
Author(s):  
Jacques Loeb

1. When a 1 per cent solution of a metal gelatinate, e.g. Na gelatinate, of pH = 8.4 is separated from distilled water by a collodion membrane, water will diffuse into the solution with a certain rate which can be measured by the rise of the level of the liquid in a manometer. When to such a solution alkali or neutral salt is added the initial rate with which water will diffuse into the solution is diminished and the more so the more alkali or salt is added. This depressing effect of the addition of alkali and neutral salt is greater when the cation of the electrolyte added is bivalent than when it is monovalent. This seems to indicate that the depressing effect is due to the cation of the electrolyte added. 2. When a neutral M/256 solution of a salt with monovalent cation (e.g. Na2SO4 or K4Fe(CN)6, etc.) is separated from distilled water by a collodion membrane, water will diffuse into the solution with a certain initial rate. When to such a solution alkali or neutral salt is added, the initial rate with which water will diffuse into the solution is diminished and the more so the more alkali or salt is added. The depressing effect of the addition of alkali or neutral salt is greater when the cation of the electrolyte added is bivalent than when it is monovalent. This seems to indicate that the depressing effect is due to the cation of the electrolyte added. The membranes used in these experiments were not treated with gelatin. 3. It can be shown that water diffuses through the collodion membrane in the form of positively charged particles under the conditions mentioned in (1) and (2). In the case of diffusion of water into a neutral solution of a salt with monovalent or bivalent cation the effect of the addition of electrolyte on the rate of diffusion can be explained on the basis of the influence of the ions on the electrification and the rate of diffusion of electrified particles of water. Since the influence of the addition of electrolyte seems to be the same in the case of solutions of metal gelatinate, the question arises whether this influence of the addition of electrolyte cannot also be explained in the same way, and, if this be true, the further question can be raised whether this depressing effect necessarily depends upon the colloidal character of the gelatin solution, or whether we are not dealing in both cases with the same property of matter; namely, the influence of ions on the electrification and rate of diffusion of water through a membrane. 4. It can be shown that the curve representing the influence of the concentration of electrolyte on the initial rate of diffusion of water from solvent into the solution through the membrane is similar to the curve representing the permanent osmotic pressure of the gelatin solution. The question which has been raised in (3) should then apply also to the influence of the concentration of ions upon the osmotic pressure and perhaps other physical properties of gelatin which depend in a similar way upon the concentration of electrolyte added; e.g., swelling. 5. When a 1 per cent solution of a gelatin-acid salt, e.g. gelatin chloride, of pH 3.4 is separated from distilled water by a collodion membrane, water will diffuse into the solution with a certain rate. When to such a solution acid or neutral salt is added—taking care in the latter case that the pH is not altered—the initial rate with which water will diffuse into the solution is diminished and the more so the more acid or salt is added. Water diffuses into a gelatin chloride solution through a collodion membrane in the form of negatively charged particles. 6. When we replace the gelatin-acid salt by a crystalloidal salt, which causes the water to diffuse through the collodion membrane in the form of negatively charged particles, e.g. M/512 Al2Cl6, we find that the addition of acid or of neutral salt will diminish the initial rate with which water diffuses into the M/512 solution of Al2Cl6, in a similar way as it does in the case of a solution of a gelatin-acid salt.


1972 ◽  
Vol 50 (5) ◽  
pp. 400-406 ◽  
Author(s):  
S. H. Song ◽  
A. C. Groom

The presence, in the feline spleen, of a slowly exchanging red cell 'compartment' ([Formula: see text] 54 min) has been demonstrated previously. These red cells adhere to reticulum cells and sinus walls in the red pulp and have been shown to be larger in cellular volume and lighter in cellular density than the rest. This suggested that they might be younger cells and we have reported briefly that they contain a high proportion of reticulocytes. Using supravital stains we have measured the percentage of reticulocytes in the outflow from isolated spleens of cats and dogs, perfused with oxygenated Ringer solution. Reticulocyte counts increased from 0.4% to 99% as the perfusion progressed. The results show that the slow compartment consists entirely of reticulocytes. The ratio of reticulocytes to rubricytes in the spleen was found to be 75:1. Therefore the reticulocytes were not produced in the spleen but were accumulated from the circulating blood. The total number of reticulocytes so stored is 1.2 × 1010 cells, equivalent to 1.5 times the daily production in the whole animal. From these data we conclude that reticulocytes released from the bone marrow under physiological conditions are sequestered and matured in the spleen.


1970 ◽  
Vol 48 (6) ◽  
pp. 359-368 ◽  
Author(s):  
B. B. Shrivastav ◽  
A. C. Burton

Previous biophysical research on the equilibrium of the red cell membrane in the normal biconcave, and the other shapes assumed in osmotic swelling, has led to a relation for the dimple region, between the tension in the membrane, its curvature, and an internal pressure. The relation is tested on a new shape produced by adding 0.004% by volume of Tween 80. The opposite membranes near the axis of revolution of the cell become parallel over a disc of diameter 2.6 μ, at a distance of 0.77 μ apart (30% less than the nearest distance in normal cells). The 'dimple' region becomes more like a 'moon crater'. The volume of the cell is not significantly altered, but the surface area increases by about 14%. The shape is consistent with a decrease in interfacial tension of the membrane, and the area increase is similar to that found by Seeman for agents which enter into the membrane. The hypothesis of internal structure across the central part of the cell, indicated by previous studies of birefringence, is supported by the observations on this new shape.


1976 ◽  
Vol 54 (4) ◽  
pp. 477-484 ◽  
Author(s):  
H. B. Geiger ◽  
S. H. Song ◽  
A. C. Groom

Isolated, denervated, cat spleens were perfused at constant flow with modified Ringer solution. Perfusion pressure, outflow rate, and outflow red cell concentration were measured against time. After splenic perfusion by 500 ml solution the cell washout curve became a single exponential function, indicating that only cells from the most slowly exchanging red cell compartment remained (these are immature and abnormal cells which adhere to the fine structures of the red pulp). Splenic contraction was induced by injection of 5 μg noradrenaline into the inflow after perfusion by 600 and 1000 ml of fluid, respectively; outflow cell concentration rose 17-fold before returning to baseline value and 32% of red cells in the spleen were expelled. The time course of changes in cell concentration was similar in shape but delayed with respect to that of outflow rate. The transit time of the cells from the site of release to the splenic vein must have exceeded 40 s, which is consistent only with release from the red pulp. Furthermore, at the peak of the cell concentration curve the mean reticulocyte count was 37.8%. Thus immature and abnormal red cells, which comprise the slowly-exchanging compartment, are indeed released from the spleen during contraction.


1926 ◽  
Vol 8 (3) ◽  
pp. 215-231 ◽  
Author(s):  
Raymond Pearl ◽  
Agnes Allen

In this paper it is shown that if the dry seeds of the cantaloupe (Cucumis melo) are soaked for 3 hours in solutions of ethyl alcohol of concentration ranging from 2 to 16 per cent by volume, and then germinated and grown in distilled water in the dark, the total growth attained is greater by amounts ranging from 9 to 35 per cent than is that made by seeds treated in every way identically except that they are initially soaked in distilled water instead of alcohol. It is shown that this result is not due simply to differences in osmotic pressure in the different alcohol solutions. It is probably due to a simple selective action of the alcohol which eliminates the constitutionally weak and defective seeds.


1927 ◽  
Vol 46 (6) ◽  
pp. 871-886 ◽  
Author(s):  
Leslie T. Webster ◽  
Caspar Burn

1. During early stages of multiplication, single cells from smooth-, mucoid-, and rough-susceptible and variant colonies show no differences in morphology or growth rate. 2. Cells from 18 to 24 hour single cell cultures of these various colony types possess similar oxygen absorption and cataphoretic migratory rates. In staining property, the cells from mucoid colonies appear larger, and those from rough colonies smaller, than the typical cells from smooth-susceptible colonies. 3. Cells from bacteriophage-resistant colonies differ from those of bacteriophage-susceptible colonies in their ability to multiply luxuriantly in the presence of bacteriophage, and in their tendency to flocculate in acid solutions at pH 3.8 to 4.1, as well as in their low degree of virulence. 4. Cells from smooth bacteriophage-susceptible colonies in contact with bacteriophage under conditions where multiplication is restrained may be altered so as to resemble the cells from the bacteriophage-resistant colonies. 5. These facts furnish evidence that bacteriophage adheres to the surface of the bacterial cell and that the various cell changes and colony alterations are of an environmental rather than genetic nature.


2005 ◽  
Vol 1054 (1) ◽  
pp. 407-416 ◽  
Author(s):  
BUNDIT WANNASUPHAPHOL ◽  
RUCHANEEKORN KALPRAVIDH ◽  
KOVIT PATTANAPANYASAT ◽  
PANOS IOANNAU ◽  
FRANS A. KUYPERS ◽  
...  
Keyword(s):  
Red Cell ◽  
Hb E ◽  

2010 ◽  
Vol 43 (1) ◽  
pp. 51-59 ◽  
Author(s):  
John R. Hess
Keyword(s):  
Red Cell ◽  

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