Leukocyte Kinetics in Hematologic Disorders Studied by DNA-Phosphorus Labeling

Author:

WALKER RICHARD I.12,HERION J. C.13,HERRING W. B.13,PALMER J. G.14

Affiliation:

1. Department of Medicine, University of North Carolina, School of Medicine, Chapel Hill, N. C.

2. University of North Carolnia School of Medicine, Chapel Hill, N. C. Scholar of the Leukemia Society, Inc., New York, N. Y.

3. University of North Carolina School of Medicine, Chapel Hill, N. C.

4. N.C.University of North Carolina School of Medicine, Chapel Hill.

Abstract

Abstract Leukocyte physiology in the normal and in hematopoietic disease states in humans has been studied by DNA-P labeling with inorganic P32. In the normal there is a post-mitotic granulocyte reservoir in marrow about 17 times the size of the intravascular compartment. Progress through this reservoir is orderly and requires about 6 days. Some 1-2 x 1011 cells daily are released from it into the blood. In polycythemia vera there is an increased production of granulocytes. DNA-P labeling in patients with chronic lymphocytic leukemia occurs at a very low level and is compatible with a very slow rate of cell renewal. In one patient with chronic lymphocytic leukemia, no disturbances in kinetics caused by a dose of 20 µc. of P32/Kg. were detected during the time of the study. Although a progressively rising concentration of label in circulating leukocyte DNA was found in patients with chronic granulocytic leukemia, without the lag suggesting a distinct marrow phase, it is concluded that the blood and extravascular leukopoietic compartments cannot be a single compartment. An essentially normal curve is obtained after induction of a complete remission with busulfan.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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