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3 - Erythropoiesis, red cells, and the approach to anemia

Published online by Cambridge University Press:  10 August 2009

Pedro A. De Alarcón
Affiliation:
St Jude Children's Research Center, Memphis, TN, USA
M. Cris Johnson
Affiliation:
Children's Hospital Central California, Madera, CA, USA
Eric J. Werner
Affiliation:
Children's Hospital of the King's Daughters, Norfolk, VA, USA
Pedro A. de Alarcón
Affiliation:
University of Tennessee
Eric J. Werner
Affiliation:
Eastern Virginia Medical School
J. Lawrence Naiman
Affiliation:
Stanford University School of Medicine, California
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Summary

Neonatal erythropoiesis

Neonatal erythropoiesis differs significantly from that in older children and adults. The birthing process with the rapid changes in oxygen concentration precipitates drastic changes in the newborn's erythroid system. To understand neonatal erythropoiesis, one needs to understand the ontogeny of erythropoiesis, from the embryo through the fetus to the newborn.

The current hypothesis of hematopoiesis is that there is a pleuripotent hematopoietic stem cell that gives rise to all hematopoietic lineages (Fig. 3.1). The ability of bone-marrow cells to reconstitute the hematopoietic system of lethally irradiated mice documented the existence of the stem cell [1]. In vitro clonogenic culture assays of bone-marrow cells documented the existence of a cascade of pluripotent and committed progenitor cells [2–6]. The commitment of the stem cell to differentiation may be a stochastic (random) or deterministic event, or a combination of both [7]. As stem cells differentiate, they lose their ability for self-renewal. Proliferation, differentiation, and survival of erythroid progenitors are dependent on the hormone erythropoietin [8]. The cascade of differentiation from the stem cell proceeds through a multipotent progenitor cell identified in vitro as colony-forming unit-granulocyte erythroid macrophage megakaryocyte (CFU-GEMM). The first recognizable pure erythroid progenitor is the burst-forming unit-erythroid (BFU-E), which then matures into the colony-forming unit-erythroid (CFU-E). The hormone erythropoietin is necessary for terminal maturation of the CFU-E. It also has an antiapoptotic effect on progenitor cells. Early progenitors depend on several cytokine mixtures for their proliferation and maturation. In utero hematopoiesis is primarily erythroid.

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Publisher: Cambridge University Press
Print publication year: 2005

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