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Research Article Free access | 10.1172/JCI107837

Hematopoiesis in the Grey Collic Dog STUDIES OF THE REGULATION OF ERYTHROPOIESIS

John W. Adamson, David C. Dale, and Ronald J. Elin

Department of Medicine, University of Washington School of Medicine, Seattle, Washington 98195

Veterans Administration Hospital, Seattle, Washington 98195

Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20014

Find articles by Adamson, J. in: PubMed | Google Scholar

Department of Medicine, University of Washington School of Medicine, Seattle, Washington 98195

Veterans Administration Hospital, Seattle, Washington 98195

Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20014

Find articles by Dale, D. in: PubMed | Google Scholar

Department of Medicine, University of Washington School of Medicine, Seattle, Washington 98195

Veterans Administration Hospital, Seattle, Washington 98195

Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20014

Find articles by Elin, R. in: PubMed | Google Scholar

Published October 1, 1974 - More info

Published in Volume 54, Issue 4 on October 1, 1974
J Clin Invest. 1974;54(4):965–973. https://doi.org/10.1172/JCI107837.
© 1974 The American Society for Clinical Investigation
Published October 1, 1974 - Version history
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Abstract

Hematopoiesis in the grey collie dog undergoes periodic fluctuations which involve reticulocytes, granulocytes, platelets, lymphocytes, and monocytes. This syndrome is inherited in an autosomal recessive manner and can be transmitted or abolished by appropriate bone marrow transplantation experiments, thus demonstrating this to be a primary marrow defect. Investigation of humoral regulation in this setting indicates that serum erythropoietin (ESF) also undergoes cyclic fluctuation and that shortly after the increase and peak in serum ESF levels recognizable red cell precursors appear in the marrow. Erythropoiesis in the grey collie is reciprocally related to the blood O2 carrying capacity. With phlebotomy, ESF activity and reticulocytes increase but continue to cycle, while hypertransfusion eliminates reticulocyte production completely. Neither phlebotomy nor hypertransfusion alter the underlying cycle time (11-12 days) nor influence the peaks of peripheral blood granulocytes. Thus, in these experiments, no direct evidence of competition between reticulocyte and granulocyte production is observed. In vitro studies of canine hemoglobin synthesis fail to demonstrate evidence of an inhibitor to ESF. These results indicate that periodic fluctuation of serum ESF is an integral part of the grey collie syndrome and are most consistent with some form of feedback regulation of ESF production.

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