Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue

Aim: To explore the feasibility of placenta tissue as a reliable and efficient source for generating mesenchymal stem cells (MSC). Methods: MSC were generated from human placenta tissue by enzymatic digestion and mechanical dissociation. The placenta MSC (PLC-MSC) were characterized for expression...

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Main Authors: Vellasamy, Shalini, Sandrasaigaran, Pratheep, Vidyadaran, Sharmili, George, Elizabeth, Ramasamy, Rajesh
Format: Article
Language:English
Published: Baishideng Publishing Group 2012
Online Access:http://psasir.upm.edu.my/id/eprint/37838/1/37838.pdf
http://psasir.upm.edu.my/id/eprint/37838/
http://www.wjgnet.com/1948-0210/abstract/v4/i6/53.htm
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spelling my.upm.eprints.378382017-10-31T03:30:33Z http://psasir.upm.edu.my/id/eprint/37838/ Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue Vellasamy, Shalini Sandrasaigaran, Pratheep Vidyadaran, Sharmili George, Elizabeth Ramasamy, Rajesh Aim: To explore the feasibility of placenta tissue as a reliable and efficient source for generating mesenchymal stem cells (MSC). Methods: MSC were generated from human placenta tissue by enzymatic digestion and mechanical dissociation. The placenta MSC (PLC-MSC) were characterized for expression of cell surface markers, embryonic stem cell (ECS) gene expression and their differentiation ability into adipocytes and osteocytes. The immunosuppressive properties of PLC-MSC on resting and phytohemagglutinin (PHA) stimulated allogenic T cells were assessed by means of cell proliferation via incorporation of tritium thymidine (3H-TdR). Results: The generated PLC-MSC appeared as spindle-shaped cells, expressed common MSC surface markers and ESC transcriptional factors. They also differentiated into adipogenic and osteogenic lineages when induced. However, continuous cultivation up to passage 15 caused changes in morphological appearance and cellular senescence, although the stem cell nature of their protein expression was unchanged. In terms of their immunosuppressive properties, PLC-MSC were unable to stimulate resting T cell proliferation; they inhibited the PHA stimulated T cells in a dose dependent manner through cell to cell contact. In our study, MSC generated from human placenta exhibited similar mesenchymal cell surface markers; MSC-like gene expression pattern and MSC-like differentiation potential were comparable to other sources of MSC. Conclusion: We suggest that placenta tissues can serve as an alternative source of MSC for future experimental and clinical studies. Baishideng Publishing Group 2012-06-26 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/37838/1/37838.pdf Vellasamy, Shalini and Sandrasaigaran, Pratheep and Vidyadaran, Sharmili and George, Elizabeth and Ramasamy, Rajesh (2012) Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue. World Journal of Stem Cells, 4 (6). pp. 53-61. ISSN 1948-0210 http://www.wjgnet.com/1948-0210/abstract/v4/i6/53.htm 10.4252/wjsc.v4.i6.53
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Aim: To explore the feasibility of placenta tissue as a reliable and efficient source for generating mesenchymal stem cells (MSC). Methods: MSC were generated from human placenta tissue by enzymatic digestion and mechanical dissociation. The placenta MSC (PLC-MSC) were characterized for expression of cell surface markers, embryonic stem cell (ECS) gene expression and their differentiation ability into adipocytes and osteocytes. The immunosuppressive properties of PLC-MSC on resting and phytohemagglutinin (PHA) stimulated allogenic T cells were assessed by means of cell proliferation via incorporation of tritium thymidine (3H-TdR). Results: The generated PLC-MSC appeared as spindle-shaped cells, expressed common MSC surface markers and ESC transcriptional factors. They also differentiated into adipogenic and osteogenic lineages when induced. However, continuous cultivation up to passage 15 caused changes in morphological appearance and cellular senescence, although the stem cell nature of their protein expression was unchanged. In terms of their immunosuppressive properties, PLC-MSC were unable to stimulate resting T cell proliferation; they inhibited the PHA stimulated T cells in a dose dependent manner through cell to cell contact. In our study, MSC generated from human placenta exhibited similar mesenchymal cell surface markers; MSC-like gene expression pattern and MSC-like differentiation potential were comparable to other sources of MSC. Conclusion: We suggest that placenta tissues can serve as an alternative source of MSC for future experimental and clinical studies.
format Article
author Vellasamy, Shalini
Sandrasaigaran, Pratheep
Vidyadaran, Sharmili
George, Elizabeth
Ramasamy, Rajesh
spellingShingle Vellasamy, Shalini
Sandrasaigaran, Pratheep
Vidyadaran, Sharmili
George, Elizabeth
Ramasamy, Rajesh
Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
author_facet Vellasamy, Shalini
Sandrasaigaran, Pratheep
Vidyadaran, Sharmili
George, Elizabeth
Ramasamy, Rajesh
author_sort Vellasamy, Shalini
title Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
title_short Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
title_full Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
title_fullStr Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
title_full_unstemmed Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
title_sort isolation and characterisation of mesenchymal stem cells derived from human placenta tissue
publisher Baishideng Publishing Group
publishDate 2012
url http://psasir.upm.edu.my/id/eprint/37838/1/37838.pdf
http://psasir.upm.edu.my/id/eprint/37838/
http://www.wjgnet.com/1948-0210/abstract/v4/i6/53.htm
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score 13.18916