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Related Concept Videos

Erythropoiesis01:14

Erythropoiesis

Red blood cells  (RBCs) transport oxygen to all body tissues. These cells survive only for 120 days and then need to be replenished. Erythropoiesis is the process of RBC production. In healthy individuals, erythropoiesis ensures all tissues are amply supplied with oxygen. In addition, blood loss due to injury leads to a drop in the physiological oxygen level that will cause erythropoiesis. Any defect in erythropoiesis leads to several physiological disorders, including thalassemia, anemia, and...
Erythropoiesis01:14

Erythropoiesis

Red blood cells  (RBCs) transport oxygen to all body tissues. These cells survive only for 120 days and then need to be replenished. Erythropoiesis is the process of RBC production. In healthy individuals, erythropoiesis ensures all tissues are amply supplied with oxygen. In addition, blood loss due to injury leads to a drop in the physiological oxygen level that will cause erythropoiesis. Any defect in erythropoiesis leads to several physiological disorders, including thalassemia, anemia, and...
Role of Hematopoietic Growth Factors01:28

Role of Hematopoietic Growth Factors

Hematopoietic growth factors are molecules that regulate the differentiation rate of hematopoietic stem cells (HSCs). Erythropoietin (EPO), primarily produced by the kidneys, plays a crucial role in erythrocyte production. When oxygen levels in the blood are low, EPO is released into the bloodstream, reaching the bone marrow, where it stimulates HSCs to differentiate and mature into erythrocytes, which are vital for oxygen transport.
Thrombopoietin (TPO), mainly released by the liver,...
Factors Affecting Erythropoiesis01:24

Factors Affecting Erythropoiesis

The cardiovascular system regulates the number of erythrocytes in the bloodstream to ensure optimal oxygen transport. It also prevents over-proliferation of these cells, which helps to maintain blood viscosity and flow rate.
Several factors influence the erythrocyte production rate, with tissue oxygen level being among the most critical. Intense exercise or high altitudes can cause tissue hypoxia, which triggers the kidneys to release more erythropoietin (EPO) into the bloodstream.
EPO then...
Overview of Hematopoiesis01:20

Overview of Hematopoiesis

Hematopoiesis, or blood cell production, is a vital biological process that begins early in embryonic development and continues throughout life. This process generates the various types of cells found in blood, including red blood cells, white blood cells, and platelets from hematopoietic stem cells (HSCs).
Developmental Phases of Hematopoiesis
Initially, HSCs are formed in the embryonic yolk sac, a critical site for early blood cell production. These stem cells subsequently migrate to other...
Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...

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A Comprehensive Pipeline to Assess the Efficiency of Human Erythropoiesis In Vitro and Ex Vivo
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Erythropoiesis: model systems, molecular regulators, and developmental programs.

Asterios S Tsiftsoglou1, Ioannis S Vizirianakis, John Strouboulis

  • 1Laboratory of Pharmacology, Department of Pharmaceutical Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece. tsif@pharm.auth.gr

IUBMB Life
|July 22, 2009
PubMed
Summary

This review details human erythropoiesis, from hematopoietic stem cells to red blood cell production. It covers regulators, signaling pathways, and gene expression, enabling customized red blood cell generation for transfusions.

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Mouse Fetal Liver Culture System to Dissect Target Gene Functions at the Early and Late Stages of Terminal Erythropoiesis
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Mouse Fetal Liver Culture System to Dissect Target Gene Functions at the Early and Late Stages of Terminal Erythropoiesis

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Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay
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Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay

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A Comprehensive Pipeline to Assess the Efficiency of Human Erythropoiesis In Vitro and Ex Vivo
08:53

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Published on: January 10, 2025

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Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay
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Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay

Published on: August 5, 2011

Area of Science:

  • Hematology
  • Developmental Biology
  • Stem Cell Biology

Background:

  • Human erythropoiesis is a complex, multistep process originating from hematopoietic stem cells (HSCs) within the bone marrow niche.
  • Erythropoiesis culminates in the production of mature erythrocytes (red blood cells, RBCs).

Purpose of the Study:

  • To provide a comprehensive review of basic and contemporary aspects of human erythropoiesis.
  • To highlight recent advancements in understanding erythroid differentiation and potential for customized RBC production.

Main Methods:

  • Review of existing literature on erythropoiesis.
  • Discussion of various model systems, including cell lines, embryonic stem cells, and knockout animal models (avian, mice, zebrafish, xenopus).
  • Analysis of key regulators, signaling pathways, transcriptional factors, and miRNAs involved in erythropoiesis.

Main Results:

  • Detailed explanation of cell-lineage pathways from HSCs to RBCs.
  • Identification of key regulators (iron, hypoxia, growth factors) and signaling pathways (SCF/c-kit, Wnt, Notch, Hox, HIF, EpoR) governing erythropoiesis.
  • Elucidation of mechanisms by which transcription factors and miRNAs regulate gene expression during erythroid differentiation, including globin gene clusters.

Conclusions:

  • Human embryonic and umbilical cord blood stem cells can differentiate into RBCs in culture using selective media.
  • Recent developments facilitate customized red blood cell production for transfusion purposes.