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Expansion of human bone marrow stromal cells on poly-(DL-lactide-co-glycolide) (PDL LGA) hollow fibres designed for use in skeletal tissue engineering

Expansion of human bone marrow stromal cells on poly-(DL-lactide-co-glycolide) (PDL LGA) hollow fibres designed for use in skeletal tissue engineering
Expansion of human bone marrow stromal cells on poly-(DL-lactide-co-glycolide) (PDL LGA) hollow fibres designed for use in skeletal tissue engineering
Strategies to expand human bone marrow stromal cells (HBMSC) for bone tissue engineering are a key to revolutionising the processes involved in three-dimensional skeletal tissue reconstruction. To facilitate this process we believe the use of biodegradable porous poly(DL-lactide-co-glycolide) (PDL LGA) hollow fibres as a scaffold used in combination with HBMSC to initiate natural bone repair and regeneration offers a potential solution. In this study, the biocompatibility of 75:25 PDL LGA fibres with HBMSC and the capacity of a PDL LGA fibre-associated HBMSC-monolayer to establish an osteogenic phenotype in vivo was examined. A high proportion of HBMSC survived when expanded on PDL LGA fibres for 6 days, with only 10% of the propidium iodide (pI)-labelled population represented in the sub-G1 DNA peak on analysis by flow cytometry. Tracking carboxy-fluorescein diacetate, succinimidyl ester (CFSE)-labelled HBMSC by flow cytometry indicated that HBMSC attachment to the P(DL)LGA fibres does not interfere with their rate of proliferation. Furthermore, in response to osteogenic stimuli, HBMSC expanded on PDL LGA fibres can differentiate, as expected, along the osteogenic lineage with associated alkaline phosphatase activity. Following implantation into SCID mice, osteogenic-conditioned PDL LGA fibre-HBMSC graft resulted in type I collagen deposition and associated bone mineralisation and osteoid formation, as evidenced by immunohistochemistry and histology. These studies provide evidence that porous PDL LGA hollow fibre-HBMSC graft is an innovative biomaterial that offers new approaches to mesenchymal cell expansion, which could be utilised as a scaffold for skeletal tissue generation.
phenotype, stem cells, lactic acid, drug effects, bone, stromal cells, human development, cells, biocompatible materials, activity, cytology, bone marrow, bone and bones, cultured, cell proliferation, disease, physiology, polyglycolic acid, health, origins, research, bone marrow cells, mice, tissue engineering, humans, analysis, acid, polymers, human, dna, tissue scaffolds, alkaline phosphatase
0142-9612
5332-5343
Morgan, S.M.
a5e72e52-d24b-4699-a5e0-7d1e8585f698
Tilley, S.
ec56245c-4ddb-48fa-943c-a2ec11a92baf
Perera, S.
0c38d531-39c4-4e33-a525-0e3f357a3468
Ellis, M.J.
5073fe05-ccc9-4a56-b664-7af550147e55
Kanczler, J.
eb8db9ff-a038-475f-9030-48eef2b0559c
Chaudhuri, J.B.
d62576e0-28fa-4e1b-8617-b7497d0a5d2e
Oreffo, R.O.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778
Morgan, S.M.
a5e72e52-d24b-4699-a5e0-7d1e8585f698
Tilley, S.
ec56245c-4ddb-48fa-943c-a2ec11a92baf
Perera, S.
0c38d531-39c4-4e33-a525-0e3f357a3468
Ellis, M.J.
5073fe05-ccc9-4a56-b664-7af550147e55
Kanczler, J.
eb8db9ff-a038-475f-9030-48eef2b0559c
Chaudhuri, J.B.
d62576e0-28fa-4e1b-8617-b7497d0a5d2e
Oreffo, R.O.
ff9fff72-6855-4d0f-bfb2-311d0e8f3778

Morgan, S.M., Tilley, S., Perera, S., Ellis, M.J., Kanczler, J., Chaudhuri, J.B. and Oreffo, R.O. (2007) Expansion of human bone marrow stromal cells on poly-(DL-lactide-co-glycolide) (PDL LGA) hollow fibres designed for use in skeletal tissue engineering. Biomaterials, 28 (35), 5332-5343. (doi:10.1016/j.biomaterials.2007.08.029).

Record type: Article

Abstract

Strategies to expand human bone marrow stromal cells (HBMSC) for bone tissue engineering are a key to revolutionising the processes involved in three-dimensional skeletal tissue reconstruction. To facilitate this process we believe the use of biodegradable porous poly(DL-lactide-co-glycolide) (PDL LGA) hollow fibres as a scaffold used in combination with HBMSC to initiate natural bone repair and regeneration offers a potential solution. In this study, the biocompatibility of 75:25 PDL LGA fibres with HBMSC and the capacity of a PDL LGA fibre-associated HBMSC-monolayer to establish an osteogenic phenotype in vivo was examined. A high proportion of HBMSC survived when expanded on PDL LGA fibres for 6 days, with only 10% of the propidium iodide (pI)-labelled population represented in the sub-G1 DNA peak on analysis by flow cytometry. Tracking carboxy-fluorescein diacetate, succinimidyl ester (CFSE)-labelled HBMSC by flow cytometry indicated that HBMSC attachment to the P(DL)LGA fibres does not interfere with their rate of proliferation. Furthermore, in response to osteogenic stimuli, HBMSC expanded on PDL LGA fibres can differentiate, as expected, along the osteogenic lineage with associated alkaline phosphatase activity. Following implantation into SCID mice, osteogenic-conditioned PDL LGA fibre-HBMSC graft resulted in type I collagen deposition and associated bone mineralisation and osteoid formation, as evidenced by immunohistochemistry and histology. These studies provide evidence that porous PDL LGA hollow fibre-HBMSC graft is an innovative biomaterial that offers new approaches to mesenchymal cell expansion, which could be utilised as a scaffold for skeletal tissue generation.

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More information

Published date: December 2007
Keywords: phenotype, stem cells, lactic acid, drug effects, bone, stromal cells, human development, cells, biocompatible materials, activity, cytology, bone marrow, bone and bones, cultured, cell proliferation, disease, physiology, polyglycolic acid, health, origins, research, bone marrow cells, mice, tissue engineering, humans, analysis, acid, polymers, human, dna, tissue scaffolds, alkaline phosphatase

Identifiers

Local EPrints ID: 61389
URI: http://eprints.soton.ac.uk/id/eprint/61389
ISSN: 0142-9612
PURE UUID: a2072700-f89b-40ed-ace6-34cced351794
ORCID for J. Kanczler: ORCID iD orcid.org/0000-0001-7249-0414
ORCID for R.O. Oreffo: ORCID iD orcid.org/0000-0001-5995-6726

Catalogue record

Date deposited: 02 Sep 2008
Last modified: 11 Jul 2024 01:43

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Contributors

Author: S.M. Morgan
Author: S. Tilley
Author: S. Perera
Author: M.J. Ellis
Author: J. Kanczler ORCID iD
Author: J.B. Chaudhuri
Author: R.O. Oreffo ORCID iD

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