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Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats
OBJECTIVES: Current treatments for osteoporosis were prevention of progression, yet it has been questionable in the stimulation of bone growth. The mesenchymal stem cells (MSCs) treatment for osteoporosis aims to induce differentiation of bone progenitor cells into bone-forming osteoblasts. We inves...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Osteoporosis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362973/ https://www.ncbi.nlm.nih.gov/pubmed/30775550 http://dx.doi.org/10.1016/j.afos.2018.08.003 |
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author | Hong, Boohwi Lee, Sunyeul Shin, Nara Ko, Youngkwon Kim, DongWoon Lee, Jun Lee, Wonhyung |
author_facet | Hong, Boohwi Lee, Sunyeul Shin, Nara Ko, Youngkwon Kim, DongWoon Lee, Jun Lee, Wonhyung |
author_sort | Hong, Boohwi |
collection | PubMed |
description | OBJECTIVES: Current treatments for osteoporosis were prevention of progression, yet it has been questionable in the stimulation of bone growth. The mesenchymal stem cells (MSCs) treatment for osteoporosis aims to induce differentiation of bone progenitor cells into bone-forming osteoblasts. We investigate whether human umbilical cord blood (hUCB)-MSCs transplantation may induce bone regeneration for osteoporotic rat model induced by ovariectomy. METHODS: The ovariectomized (OVX) group (n = 10) and OVX-MSCs group (n = 10) underwent bilateral ovariectomy to induce osteoporosis, while the Sham group (n = 10) underwent sham operation at aged 12 weeks. After a femoral defect was made at 9 months, Sham group and OVX group were injected with Hartmann solution, while the OVX-MSCs group was injected with Hartmann solution containing 1 × 10(7) hUCB-MSCs. The volume of regenerated bone was evaluated using micro-computed tomography at 4 and 8 weeks postoperation. RESULTS: At 4- and 8-week postoperation, the OVX group (5.0% ± 1.5%; 6.1% ± 0.7%) had a significantly lower regenerated bone volume than the Sham group (8.6% ± 1.3%; 12.0% ± 1.8%, P < 0.01), respectively. However, there was no significant difference between the OVX-MSCs and Sham groups. The OVX-MSCs group resulted in about 53% and 65% significantly higher new bone formation than the OVX group (7.7% ± 1.9%; 10.0% ± 2.9%, P < 0.05). CONCLUSIONS: hUCB-MSCs in bone defects may enhance bone regeneration in osteoporotic rat model similar to nonosteoporotic bone regeneration. hUCB-MSCs may be a promising alternative stem cell therapy for osteoporosis. |
format | Online Article Text |
id | pubmed-6362973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society of Osteoporosis |
record_format | MEDLINE/PubMed |
spelling | pubmed-63629732019-02-15 Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats Hong, Boohwi Lee, Sunyeul Shin, Nara Ko, Youngkwon Kim, DongWoon Lee, Jun Lee, Wonhyung Osteoporos Sarcopenia Original Article OBJECTIVES: Current treatments for osteoporosis were prevention of progression, yet it has been questionable in the stimulation of bone growth. The mesenchymal stem cells (MSCs) treatment for osteoporosis aims to induce differentiation of bone progenitor cells into bone-forming osteoblasts. We investigate whether human umbilical cord blood (hUCB)-MSCs transplantation may induce bone regeneration for osteoporotic rat model induced by ovariectomy. METHODS: The ovariectomized (OVX) group (n = 10) and OVX-MSCs group (n = 10) underwent bilateral ovariectomy to induce osteoporosis, while the Sham group (n = 10) underwent sham operation at aged 12 weeks. After a femoral defect was made at 9 months, Sham group and OVX group were injected with Hartmann solution, while the OVX-MSCs group was injected with Hartmann solution containing 1 × 10(7) hUCB-MSCs. The volume of regenerated bone was evaluated using micro-computed tomography at 4 and 8 weeks postoperation. RESULTS: At 4- and 8-week postoperation, the OVX group (5.0% ± 1.5%; 6.1% ± 0.7%) had a significantly lower regenerated bone volume than the Sham group (8.6% ± 1.3%; 12.0% ± 1.8%, P < 0.01), respectively. However, there was no significant difference between the OVX-MSCs and Sham groups. The OVX-MSCs group resulted in about 53% and 65% significantly higher new bone formation than the OVX group (7.7% ± 1.9%; 10.0% ± 2.9%, P < 0.05). CONCLUSIONS: hUCB-MSCs in bone defects may enhance bone regeneration in osteoporotic rat model similar to nonosteoporotic bone regeneration. hUCB-MSCs may be a promising alternative stem cell therapy for osteoporosis. Korean Society of Osteoporosis 2018-09 2018-09-26 /pmc/articles/PMC6362973/ /pubmed/30775550 http://dx.doi.org/10.1016/j.afos.2018.08.003 Text en © 2018 The Korean Society of Osteoporosis. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Hong, Boohwi Lee, Sunyeul Shin, Nara Ko, Youngkwon Kim, DongWoon Lee, Jun Lee, Wonhyung Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
title | Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
title_full | Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
title_fullStr | Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
title_full_unstemmed | Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
title_short | Bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
title_sort | bone regeneration with umbilical cord blood mesenchymal stem cells in femoral defects of ovariectomized rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362973/ https://www.ncbi.nlm.nih.gov/pubmed/30775550 http://dx.doi.org/10.1016/j.afos.2018.08.003 |
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