Literature DB >> 1698550

Differential effect of pH on the density and volume of rat reticulocytes and erythrocytes. Relevance to their fractionation by centrifugation.

H Walter1, E J Krob, R B Wenby, H J Meiselman.   

Abstract

Rats were injected with 59Fe-ferrous citrate and bled thereafter at different times (16 h to 49 d). This gave rise to red cell populations in which cells corresponding in age to the time elapsed between injection and bleeding were labeled. The anticoagulant used was either acid-citrate-dextrose (ACD) with a pH adjusted to 7.3 or ACD (pH 5.1). Final pH of the collected blood was about 7.2-7.4 in the former case and 6.4-6.7 in the latter. Red cells were then centrifuged (5) and approximately 7-10% of the packed cells from the top and 7-10% from the bottom of the cell column collected. When reticulocytes are the predominant labeled red cell population, as in blood obtained for about 24 h after isotope injection, a fractionation of these cells and mature erythrocytes is in evidence only when blood is collected at the higher pH. Thus, at pH 7.2-7.4 ratios of specific radioactivities of cells in top fraction/cells in an unfractionated sample are about 3, whereas at pH 6.4-6.7, the analogous ratios are 1 or less. These differences in specific activity ratios, as a function of pH at collection, virtually disappear after about 4 d following isotope injection. The lower pH is known to increase the volume and decrease the density of mature red blood cells. The marked effect of pH on cellular fractionation could be correlated with the smaller change in rat reticulocyte density and volume in acid medium. At pH 6.4-6.7, the densities of mature erythrocytes and reticulocytes are so close that their physical separation by centrifugation is not feasible.

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Year:  1990        PMID: 1698550     DOI: 10.1007/bf02991427

Source DB:  PubMed          Journal:  Cell Biophys        ISSN: 0163-4992


  13 in total

1.  Effect of surface modification of rat erythrocytes of different ages on their partitioning behavior in charge-sensitive two-polymer aqueous phases.

Authors:  H Walter; E J Krob; A Pedram; C H Tamblyn; G V Seaman
Journal:  Biochim Biophys Acta       Date:  1986-09-11

2.  Influence of temperature and method of centrifugation on the separation of erythrocytes.

Authors:  J R Murphy
Journal:  J Lab Clin Med       Date:  1973-08

3.  The determination of the partial specific volume of proteins by the mechanical oscillator technique.

Authors:  O Kratky; H Leopold; H Stabinger
Journal:  Methods Enzymol       Date:  1973       Impact factor: 1.600

4.  Membrane surface properties of reticulocytes from rats rendered severely anemic with phenylhydrazine as determined by partition in aqueous phase systems.

Authors:  H Walter; A Miller; E J Krob; G S Ascher
Journal:  Exp Cell Res       Date:  1972-07       Impact factor: 3.905

5.  Surface alterations of erythrocytes with cell age: rat red cell is not a model for human red cell.

Authors:  H Walter; E J Krob; C H Tamblyn; G V Seaman
Journal:  Biochem Biophys Res Commun       Date:  1980-11-17       Impact factor: 3.575

Review 6.  Senescence of red blood cells: progress and problems.

Authors:  M R Clark
Journal:  Physiol Rev       Date:  1988-04       Impact factor: 37.312

7.  Separation of rabbit red cells by density in a bovine serum albumin gradient and correlation of red cell density with cell age after in vivo labeling with 59-Fe.

Authors:  C Bishop; T C Prentice
Journal:  J Cell Physiol       Date:  1966-02       Impact factor: 6.384

8.  Na+-K+ transport and volume of rat erythrocytes under dietary K+ deficiency.

Authors:  J Duhm; B O Göbel
Journal:  Am J Physiol       Date:  1984-01

9.  Volume-stimulated, Cl(-)-dependent K+ efflux is highly expressed in young human red cells containing normal hemoglobin or HbS.

Authors:  M Canessa; M E Fabry; N Blumenfeld; R L Nagel
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

10.  The separation of different cell classes from lymphoid organs. 3. Te purfication of erythroid cells by pH-induced density changes.

Authors:  K Shortman; K Seligman
Journal:  J Cell Biol       Date:  1969-09       Impact factor: 10.539

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