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Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence
Scientific Reports, Volume: 7, Issue: 1, Start page: 41421
Swansea University Authors: Christopher Fellows, Charles Archer, Ilyas Khan
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DOI (Published version): 10.1038/srep41421
Abstract
In recent years it has become increasingly clear that articular cartilage harbours a viable pool ofprogenitor cells and interest has focussed on their role during development and disease. Analysis ofprogenitor numbers using fluorescence-activated sorting techniques has resulted in wide-rangingestima...
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ISSN: | 2045-2322 |
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Springer Science and Business Media LLC
2017
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2020-07-31T14:31:10.9919346 v2 31768 2017-01-26 Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence f720be0016a59d4dab49bc956c1c242a Christopher Fellows Christopher Fellows true false d23ecc9643761bda7acd0f488ed0783e Charles Archer Charles Archer true false 2536d955ff70e7b77063a8efe9103161 0000-0002-3886-1987 Ilyas Khan Ilyas Khan true false 2017-01-26 FGMHL In recent years it has become increasingly clear that articular cartilage harbours a viable pool ofprogenitor cells and interest has focussed on their role during development and disease. Analysis ofprogenitor numbers using fluorescence-activated sorting techniques has resulted in wide-rangingestimates, which may be the result of context-dependent expression of cell surface markers. Wehave used a colony-forming assay to reliably determine chondroprogenitor numbers in normal andosteoarthritic cartilage where we observed a 2-fold increase in diseased tissue (P < 0.0001). Intriguingly,cell kinetic analysis of clonal isolates derived from single and multiple donors of osteoarthritic cartilagerevealed the presence of a divergent progenitor subpopulation characterised by an early senescentphenotype. Divergent sub-populations displayed increased senescence-associated β–galactosidaseactivity, lower average telomere lengths but retained the capacity to undergo multi-lineagedifferentiation. Osteoarthritis is an age-related disease and cellular senescence is predicted to be asignificant component of the pathological process. This study shows that although early senescenceis an inherent property of a subset of activated progenitors, there is also a pool of progenitors withextended viability and regenerative potential residing within osteoarthritic cartilage. Journal Article Scientific Reports 7 1 41421 Springer Science and Business Media LLC 2045-2322 2 2 2017 2017-02-02 10.1038/srep41421 COLLEGE NANME Medicine, Health and Life Science - Faculty COLLEGE CODE FGMHL Swansea University 2020-07-31T14:31:10.9919346 2017-01-26T11:51:49.5483918 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Christopher Fellows 1 Rebecca Williams 2 Iwan R. Davies 3 Kajal Gohil 4 Duncan M. Baird 5 John Fairclough 6 Paul Rooney 7 Charles Archer 8 Ilyas Khan 0000-0002-3886-1987 9 0031768-15022017131015.pdf srep41421.pdf 2017-02-15T13:10:15.2870000 Output 1478311 application/pdf Version of Record true 2017-02-02T00:00:00.0000000 This work is licensed under a Creative Commons Attribution 4.0 International License. true eng http://creativecommons.org/licenses/by/4.0/ |
title |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence |
spellingShingle |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence Christopher Fellows Charles Archer Ilyas Khan |
title_short |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence |
title_full |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence |
title_fullStr |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence |
title_full_unstemmed |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence |
title_sort |
Characterisation of a divergent progenitor cell sub-populations in human osteoarthritic cartilage: the role of telomere erosion and replicative senescence |
author_id_str_mv |
f720be0016a59d4dab49bc956c1c242a d23ecc9643761bda7acd0f488ed0783e 2536d955ff70e7b77063a8efe9103161 |
author_id_fullname_str_mv |
f720be0016a59d4dab49bc956c1c242a_***_Christopher Fellows d23ecc9643761bda7acd0f488ed0783e_***_Charles Archer 2536d955ff70e7b77063a8efe9103161_***_Ilyas Khan |
author |
Christopher Fellows Charles Archer Ilyas Khan |
author2 |
Christopher Fellows Rebecca Williams Iwan R. Davies Kajal Gohil Duncan M. Baird John Fairclough Paul Rooney Charles Archer Ilyas Khan |
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Scientific Reports |
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41421 |
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Swansea University |
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10.1038/srep41421 |
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Springer Science and Business Media LLC |
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Faculty of Medicine, Health and Life Sciences |
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description |
In recent years it has become increasingly clear that articular cartilage harbours a viable pool ofprogenitor cells and interest has focussed on their role during development and disease. Analysis ofprogenitor numbers using fluorescence-activated sorting techniques has resulted in wide-rangingestimates, which may be the result of context-dependent expression of cell surface markers. Wehave used a colony-forming assay to reliably determine chondroprogenitor numbers in normal andosteoarthritic cartilage where we observed a 2-fold increase in diseased tissue (P < 0.0001). Intriguingly,cell kinetic analysis of clonal isolates derived from single and multiple donors of osteoarthritic cartilagerevealed the presence of a divergent progenitor subpopulation characterised by an early senescentphenotype. Divergent sub-populations displayed increased senescence-associated β–galactosidaseactivity, lower average telomere lengths but retained the capacity to undergo multi-lineagedifferentiation. Osteoarthritis is an age-related disease and cellular senescence is predicted to be asignificant component of the pathological process. This study shows that although early senescenceis an inherent property of a subset of activated progenitors, there is also a pool of progenitors withextended viability and regenerative potential residing within osteoarthritic cartilage. |
published_date |
2017-02-02T03:38:48Z |
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1763751733666775040 |
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11.037603 |