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Erythropoiesis is the production of haemoglobin-containing red blood cells for oxygen delivery to the tissues. Approximately 1-2 Ã- 1012red cells are produced each day, and this remarkable productivity under stable conditions is also complemented by the capacity for rapid and substantial expansion when required. This chapter describes the developmental origins of primitive and definitive erythropoiesis in the yolk sac, the fetal liver and the bone marrow. Our current understanding of the mechanisms of erythroid lineage specification from multipotent haemopoietic stem cells remains incomplete, but key erythroid-specific transcription factors are known to be critical in directing erythroid-specific transcription. Characteristic changes in morphology, gene expression and cell surface markers allow the identification of erythroid cells at different stages of their differentiation and maturation. At a system level, the hormone erythropoietin is the principal regulator of erythroid activity. Following upregulation of its transcription by Hypoxia-Inducible Factor, erythropoietin directs an expansion of the pool of erythroid precursors and accelerated red cell maturation. This, together with coordinated iron absorption and delivery, provides an appropriate response to hypoxia caused by reduced numbers of circulating red blood cells associated with a very wide spectrum of causes.

Original publication

DOI

10.1002/9781119706687.ch3

Type

Chapter

Book title

Hoffbrand S Postgraduate Haematology Eighth Edition

Publication Date

01/01/2025

Pages

43 - 55