Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat

Study Design. Isolation and characterization of human epidural fat (HEF) stem/progenitor cells. Objective. To identify a progenitor population within HEF and to determine if they meet the minimal criteria of a mesenchymal stem cell (MSC). Summary of Background Data. The biological function, if any,...

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Main Authors: Nedaa Al-Jezani, Roger Cho, Anand O. Masson, Brian Lenehan, Roman Krawetz, Frank G. Lyons
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2019/2175273
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author Nedaa Al-Jezani
Roger Cho
Anand O. Masson
Brian Lenehan
Roman Krawetz
Frank G. Lyons
author_facet Nedaa Al-Jezani
Roger Cho
Anand O. Masson
Brian Lenehan
Roman Krawetz
Frank G. Lyons
author_sort Nedaa Al-Jezani
collection DOAJ
description Study Design. Isolation and characterization of human epidural fat (HEF) stem/progenitor cells. Objective. To identify a progenitor population within HEF and to determine if they meet the minimal criteria of a mesenchymal stem cell (MSC). Summary of Background Data. The biological function, if any, has yet to be determined for HEF. The presence of MSCs within HEF may indicate a regenerative potential within the HEF. Methods. HEF was isolated from 10 patients during elective spinal surgery. HEF cells were differentiated along osteo-, adipo-, and chondrogenic lineages, with differentiation analyzed via qPCR and histology. The cell surface receptor profile of HEF cells was examined by flow cytometry. HEF cells were also assayed through the collagen contraction assay. Prx1CreERT2GFP:R26RTdTomato MSC lineage-tracking mice were employed to identify EF MSCs in vivo. Results. HEF cell lines were obtained from all 10 patients in the study. Cells from 2/10 patients demonstrated full MSC potential, while cells from 6/10 patients demonstrated progenitor potential; 2/10 patients presented with cells that retained only adipogenic potential. HEF cells demonstrated MSC surface marker expression. All patient cell lines contracted collagen gels. A Prx1-positive population in mouse epidural fat that appeared to contribute to the dura of the spinal cord was observed in vivo. Conclusions. MSC and progenitor populations are present within HEF. MSCs were not identified in all patients examined in the current study. Furthermore, all patient lines demonstrated collagen contraction capacity, suggesting either a contaminating activated fibroblast population or HEF MSCs/progenitors also demonstrating a fibroblast-like phenotype. In vivo analysis suggests that these cell populations may contribute to the dura. Overall, these results suggest that cells within epidural fat may play a biological role within the local environment above providing a mechanical buffer.
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spelling doaj-art-82b2fac9603d49fdb7f194b8a4dc586e2025-02-03T01:24:17ZengWileyStem Cells International1687-966X1687-96782019-01-01201910.1155/2019/21752732175273Isolation and Characterization of an Adult Stem Cell Population from Human Epidural FatNedaa Al-Jezani0Roger Cho1Anand O. Masson2Brian Lenehan3Roman Krawetz4Frank G. Lyons5McCaig Institute for Bone and Joint Health, University of Calgary, CanadaMcCaig Institute for Bone and Joint Health, University of Calgary, CanadaMcCaig Institute for Bone and Joint Health, University of Calgary, CanadaUniversity Hospital Limerick and Mater Misericordiae University Hospital, IrelandMcCaig Institute for Bone and Joint Health, University of Calgary, CanadaDivision of Orthopaedic Surgery, Foothills Medical Centre, Calgary, CanadaStudy Design. Isolation and characterization of human epidural fat (HEF) stem/progenitor cells. Objective. To identify a progenitor population within HEF and to determine if they meet the minimal criteria of a mesenchymal stem cell (MSC). Summary of Background Data. The biological function, if any, has yet to be determined for HEF. The presence of MSCs within HEF may indicate a regenerative potential within the HEF. Methods. HEF was isolated from 10 patients during elective spinal surgery. HEF cells were differentiated along osteo-, adipo-, and chondrogenic lineages, with differentiation analyzed via qPCR and histology. The cell surface receptor profile of HEF cells was examined by flow cytometry. HEF cells were also assayed through the collagen contraction assay. Prx1CreERT2GFP:R26RTdTomato MSC lineage-tracking mice were employed to identify EF MSCs in vivo. Results. HEF cell lines were obtained from all 10 patients in the study. Cells from 2/10 patients demonstrated full MSC potential, while cells from 6/10 patients demonstrated progenitor potential; 2/10 patients presented with cells that retained only adipogenic potential. HEF cells demonstrated MSC surface marker expression. All patient cell lines contracted collagen gels. A Prx1-positive population in mouse epidural fat that appeared to contribute to the dura of the spinal cord was observed in vivo. Conclusions. MSC and progenitor populations are present within HEF. MSCs were not identified in all patients examined in the current study. Furthermore, all patient lines demonstrated collagen contraction capacity, suggesting either a contaminating activated fibroblast population or HEF MSCs/progenitors also demonstrating a fibroblast-like phenotype. In vivo analysis suggests that these cell populations may contribute to the dura. Overall, these results suggest that cells within epidural fat may play a biological role within the local environment above providing a mechanical buffer.http://dx.doi.org/10.1155/2019/2175273
spellingShingle Nedaa Al-Jezani
Roger Cho
Anand O. Masson
Brian Lenehan
Roman Krawetz
Frank G. Lyons
Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat
Stem Cells International
title Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat
title_full Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat
title_fullStr Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat
title_full_unstemmed Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat
title_short Isolation and Characterization of an Adult Stem Cell Population from Human Epidural Fat
title_sort isolation and characterization of an adult stem cell population from human epidural fat
url http://dx.doi.org/10.1155/2019/2175273
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