Cellular Reprogramming toward the Erythroid Lineage

Haemoglobinopathies such as thalassaemia and sickle cell disease present a major health burden. Currently, the main forms of treatment for these diseases are packed red blood cell transfusions and the administration of drugs which act to nonspecifically reactivate the production of foetal haemoglobi...

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Main Authors: Laura J. Norton, Alister P. W. Funnell, Richard C. M. Pearson, Merlin Crossley
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:International Journal of Cell Biology
Online Access:http://dx.doi.org/10.1155/2011/501464
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author Laura J. Norton
Alister P. W. Funnell
Richard C. M. Pearson
Merlin Crossley
author_facet Laura J. Norton
Alister P. W. Funnell
Richard C. M. Pearson
Merlin Crossley
author_sort Laura J. Norton
collection DOAJ
description Haemoglobinopathies such as thalassaemia and sickle cell disease present a major health burden. Currently, the main forms of treatment for these diseases are packed red blood cell transfusions and the administration of drugs which act to nonspecifically reactivate the production of foetal haemoglobin. These treatments are ongoing throughout the life of the patient and are associated with a number of risks, such as limitations in available blood for transfusion, infections, iron overload, immune rejection, and side effects associated with the drug treatments. The field of cellular reprogramming has advanced significantly in the last few years and has recently culminated in the successful production of erythrocytes in culture. This paper will discuss cellular reprogramming and its potential relevance to the treatment of haemoglobinopathies.
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publishDate 2011-01-01
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series International Journal of Cell Biology
spelling doaj-art-bc1456c5e68640488a5ed89db7907bd52025-02-03T05:54:20ZengWileyInternational Journal of Cell Biology1687-88761687-88842011-01-01201110.1155/2011/501464501464Cellular Reprogramming toward the Erythroid LineageLaura J. Norton0Alister P. W. Funnell1Richard C. M. Pearson2Merlin Crossley3School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, AustraliaSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, AustraliaSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, AustraliaSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, AustraliaHaemoglobinopathies such as thalassaemia and sickle cell disease present a major health burden. Currently, the main forms of treatment for these diseases are packed red blood cell transfusions and the administration of drugs which act to nonspecifically reactivate the production of foetal haemoglobin. These treatments are ongoing throughout the life of the patient and are associated with a number of risks, such as limitations in available blood for transfusion, infections, iron overload, immune rejection, and side effects associated with the drug treatments. The field of cellular reprogramming has advanced significantly in the last few years and has recently culminated in the successful production of erythrocytes in culture. This paper will discuss cellular reprogramming and its potential relevance to the treatment of haemoglobinopathies.http://dx.doi.org/10.1155/2011/501464
spellingShingle Laura J. Norton
Alister P. W. Funnell
Richard C. M. Pearson
Merlin Crossley
Cellular Reprogramming toward the Erythroid Lineage
International Journal of Cell Biology
title Cellular Reprogramming toward the Erythroid Lineage
title_full Cellular Reprogramming toward the Erythroid Lineage
title_fullStr Cellular Reprogramming toward the Erythroid Lineage
title_full_unstemmed Cellular Reprogramming toward the Erythroid Lineage
title_short Cellular Reprogramming toward the Erythroid Lineage
title_sort cellular reprogramming toward the erythroid lineage
url http://dx.doi.org/10.1155/2011/501464
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