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Cell fusion in the brain: two cells forward, one cell back
Adult stem cell populations, notably those which reside in the bone marrow, have been shown to contribute to several neuronal cell types in the rodent and human brain. The observation that circulating bone marrow cells can migrate into the central nervous system and fuse with, in particular, cerebel...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201757/ https://www.ncbi.nlm.nih.gov/pubmed/24899142 http://dx.doi.org/10.1007/s00401-014-1303-1 |
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author | Kemp, Kevin Wilkins, Alastair Scolding, Neil |
author_facet | Kemp, Kevin Wilkins, Alastair Scolding, Neil |
author_sort | Kemp, Kevin |
collection | PubMed |
description | Adult stem cell populations, notably those which reside in the bone marrow, have been shown to contribute to several neuronal cell types in the rodent and human brain. The observation that circulating bone marrow cells can migrate into the central nervous system and fuse with, in particular, cerebellar Purkinje cells has suggested, at least in part, a potential mechanism behind this process. Experimentally, the incidence of cell fusion in the brain is enhanced with age, radiation exposure, inflammation, chemotherapeutic drugs and even selective damage to the neurons themselves. The presence of cell fusion, shown by detection of increased bi-nucleated neurons, has also been described in a variety of human central nervous system diseases, including both multiple sclerosis and Alzheimer’s disease. Accumulating evidence is therefore raising new questions into the biological significance of cell fusion, with the possibility that it represents an important means of cell-mediated neuroprotection or rescue of highly complex neurons that cannot be replaced in adult life. Here, we discuss the evidence behind this phenomenon in the rodent and human brain, with a focus on the subsequent research investigating the physiological mechanisms of cell fusion underlying this process. We also highlight how these studies offer new insights into endogenous neuronal repair, opening new exciting avenues for potential therapeutic interventions against neurodegeneration and brain injury. |
format | Online Article Text |
id | pubmed-4201757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-42017572014-10-22 Cell fusion in the brain: two cells forward, one cell back Kemp, Kevin Wilkins, Alastair Scolding, Neil Acta Neuropathol Review Adult stem cell populations, notably those which reside in the bone marrow, have been shown to contribute to several neuronal cell types in the rodent and human brain. The observation that circulating bone marrow cells can migrate into the central nervous system and fuse with, in particular, cerebellar Purkinje cells has suggested, at least in part, a potential mechanism behind this process. Experimentally, the incidence of cell fusion in the brain is enhanced with age, radiation exposure, inflammation, chemotherapeutic drugs and even selective damage to the neurons themselves. The presence of cell fusion, shown by detection of increased bi-nucleated neurons, has also been described in a variety of human central nervous system diseases, including both multiple sclerosis and Alzheimer’s disease. Accumulating evidence is therefore raising new questions into the biological significance of cell fusion, with the possibility that it represents an important means of cell-mediated neuroprotection or rescue of highly complex neurons that cannot be replaced in adult life. Here, we discuss the evidence behind this phenomenon in the rodent and human brain, with a focus on the subsequent research investigating the physiological mechanisms of cell fusion underlying this process. We also highlight how these studies offer new insights into endogenous neuronal repair, opening new exciting avenues for potential therapeutic interventions against neurodegeneration and brain injury. Springer Berlin Heidelberg 2014-06-05 2014 /pmc/articles/PMC4201757/ /pubmed/24899142 http://dx.doi.org/10.1007/s00401-014-1303-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Review Kemp, Kevin Wilkins, Alastair Scolding, Neil Cell fusion in the brain: two cells forward, one cell back |
title | Cell fusion in the brain: two cells forward, one cell back |
title_full | Cell fusion in the brain: two cells forward, one cell back |
title_fullStr | Cell fusion in the brain: two cells forward, one cell back |
title_full_unstemmed | Cell fusion in the brain: two cells forward, one cell back |
title_short | Cell fusion in the brain: two cells forward, one cell back |
title_sort | cell fusion in the brain: two cells forward, one cell back |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201757/ https://www.ncbi.nlm.nih.gov/pubmed/24899142 http://dx.doi.org/10.1007/s00401-014-1303-1 |
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