Literature DB >> 2326648

Erythropoietin retards DNA breakdown and prevents programmed death in erythroid progenitor cells.

M J Koury1, M C Bondurant.   

Abstract

The mechanism by which erythropoietin controls mammalian erythrocyte production is unknown. Labeling experiments in vitro with [3H]thymidine demonstrated DNA cleavage in erythroid progenitor cells that was accompanied by DNA repair and synthesis. Erythropoietin reduced DNA cleavage by a factor of 2.6. In the absence of erythropoietin, erythroid progenitor cells accumulated DNA cleavage fragments characteristic of those found in programmed cell death (apoptosis) by 2 to 4 hours and began dying by 16 hours. In the presence of erythropoietin, the progenitor cells survived and differentiated into reticulocytes. Thus, apoptosis is a major component of normal erythropoiesis, and erythropoietin controls erythrocyte production by retarding DNA breakdown and preventing apoptosis in erythroid progenitor cells.

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Year:  1990        PMID: 2326648     DOI: 10.1126/science.2326648

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  170 in total

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Review 4.  Apoptosis and the regulation of cell numbers in normal and neoplastic tissues: an overview.

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Journal:  Cancer Metastasis Rev       Date:  1992-09       Impact factor: 9.264

5.  A simple and rapid method for detection of apoptosis in human cells.

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Review 6.  A free-radical hypothesis for the instability and evolution of genotype and phenotype in vitro.

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8.  Immature erythroblasts with extensive ex vivo self-renewal capacity emerge from the early mammalian fetus.

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Journal:  Blood       Date:  2010-12-02       Impact factor: 22.113

9.  Functional conservation of erythropoietin signaling in zebrafish.

Authors:  Noëlle Paffett-Lugassy; Nelson Hsia; Paula G Fraenkel; Barry Paw; Irene Leshinsky; Bruce Barut; Nathan Bahary; Jaime Caro; Robert Handin; Leonard I Zon
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10.  Mesangial cell apoptosis: the major mechanism for resolution of glomerular hypercellularity in experimental mesangial proliferative nephritis.

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