Transplantation of embryonic fibroblasts treated with platelet-rich plasma induces osteogenesis in SAMP8 mice monitored by molecular imaging

Wen Cheng Lo, Jeng Fong Chiou, Juri G. Gelovani, Mei Leng Cheong, Chi-Ming Lee, Hen Yu Liu, Chih Hsiung Wu, Ming Fu Wang, Che Tong Lin, Win Ping Deng

研究成果: 雜誌貢獻文章

24 引文 (Scopus)

摘要

The aim of this study was to develop a cell-based boneregeneration approach evaluated by molecular imaging and immunohistochemistry. Methods: Genetically modified NIH3T3 embryonic fibroblasts carrying enhanced green fluorescent protein (NIH3T3-G) were predifferentiated into osteoblastlike cells using platelet-rich plasma (PRP) medium, followed by intraosseous transplantation into ovariectomized senescenceaccelerated mouse prone substrain 8 (OVX-SAMP8 mice). Results: PRP-conditioned NIH3T3-G (PRP/NIH3T3-G) engraftment prevented the development of osteoporosis. Molecular imaging and immunohistochemistry demonstrated the migration of NIH3T3-G cells from the implantation site throughout the skeleton. In situ analyses revealed coexpression of osteopontin and green fluorescent protein in the newly formed bone tissue, demonstrating that the transplant restored the bone trabecular architecture and mineral density in treated OVX-SAMP8 mice. Interestingly, the life span of OVX-SAMP8 mice receiving PRP/NIH3T3-G transplantation was significantly prolonged and similar to that of the congenic senescence-resistant strain of mice. Conclusion: This unique and yet simple approach could potentially be applied to the treatment of senile postmenopausal osteoporosis and perhaps inborn genetic syndromes associated with accelerated aging, such asHutchinson-Gilford progeria syndrome, and for the prolongation of life expectancy in general.
原文英語
頁(從 - 到)765-773
頁數9
期刊Journal of Nuclear Medicine
50
發行號5
DOIs
出版狀態已發佈 - 五月 1 2009

指紋

Molecular Imaging
Platelet-Rich Plasma
Osteogenesis
Fibroblasts
Transplantation
Osteoporosis
Immunohistochemistry
Progeria
Life Support Care
Gastrin-Secreting Cells
Postmenopausal Osteoporosis
Osteopontin
Life Expectancy
Green Fluorescent Proteins
Skeleton
Minerals
Transplants
Bone and Bones

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

引用此文

Transplantation of embryonic fibroblasts treated with platelet-rich plasma induces osteogenesis in SAMP8 mice monitored by molecular imaging. / Lo, Wen Cheng; Chiou, Jeng Fong; Gelovani, Juri G.; Cheong, Mei Leng; Lee, Chi-Ming; Liu, Hen Yu; Wu, Chih Hsiung; Wang, Ming Fu; Lin, Che Tong; Deng, Win Ping.

於: Journal of Nuclear Medicine, 卷 50, 編號 5, 01.05.2009, p. 765-773.

研究成果: 雜誌貢獻文章

Lo, Wen Cheng ; Chiou, Jeng Fong ; Gelovani, Juri G. ; Cheong, Mei Leng ; Lee, Chi-Ming ; Liu, Hen Yu ; Wu, Chih Hsiung ; Wang, Ming Fu ; Lin, Che Tong ; Deng, Win Ping. / Transplantation of embryonic fibroblasts treated with platelet-rich plasma induces osteogenesis in SAMP8 mice monitored by molecular imaging. 於: Journal of Nuclear Medicine. 2009 ; 卷 50, 編號 5. 頁 765-773.
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abstract = "The aim of this study was to develop a cell-based boneregeneration approach evaluated by molecular imaging and immunohistochemistry. Methods: Genetically modified NIH3T3 embryonic fibroblasts carrying enhanced green fluorescent protein (NIH3T3-G) were predifferentiated into osteoblastlike cells using platelet-rich plasma (PRP) medium, followed by intraosseous transplantation into ovariectomized senescenceaccelerated mouse prone substrain 8 (OVX-SAMP8 mice). Results: PRP-conditioned NIH3T3-G (PRP/NIH3T3-G) engraftment prevented the development of osteoporosis. Molecular imaging and immunohistochemistry demonstrated the migration of NIH3T3-G cells from the implantation site throughout the skeleton. In situ analyses revealed coexpression of osteopontin and green fluorescent protein in the newly formed bone tissue, demonstrating that the transplant restored the bone trabecular architecture and mineral density in treated OVX-SAMP8 mice. Interestingly, the life span of OVX-SAMP8 mice receiving PRP/NIH3T3-G transplantation was significantly prolonged and similar to that of the congenic senescence-resistant strain of mice. Conclusion: This unique and yet simple approach could potentially be applied to the treatment of senile postmenopausal osteoporosis and perhaps inborn genetic syndromes associated with accelerated aging, such asHutchinson-Gilford progeria syndrome, and for the prolongation of life expectancy in general.",
keywords = "Bone, Molecular biology, Molecular imaging, Osteogenesis, Platelet-rich plasma, Senescence-accelerated mice P8, Transplantation",
author = "Lo, {Wen Cheng} and Chiou, {Jeng Fong} and Gelovani, {Juri G.} and Cheong, {Mei Leng} and Chi-Ming Lee and Liu, {Hen Yu} and Wu, {Chih Hsiung} and Wang, {Ming Fu} and Lin, {Che Tong} and Deng, {Win Ping}",
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AU - Lo, Wen Cheng

AU - Chiou, Jeng Fong

AU - Gelovani, Juri G.

AU - Cheong, Mei Leng

AU - Lee, Chi-Ming

AU - Liu, Hen Yu

AU - Wu, Chih Hsiung

AU - Wang, Ming Fu

AU - Lin, Che Tong

AU - Deng, Win Ping

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N2 - The aim of this study was to develop a cell-based boneregeneration approach evaluated by molecular imaging and immunohistochemistry. Methods: Genetically modified NIH3T3 embryonic fibroblasts carrying enhanced green fluorescent protein (NIH3T3-G) were predifferentiated into osteoblastlike cells using platelet-rich plasma (PRP) medium, followed by intraosseous transplantation into ovariectomized senescenceaccelerated mouse prone substrain 8 (OVX-SAMP8 mice). Results: PRP-conditioned NIH3T3-G (PRP/NIH3T3-G) engraftment prevented the development of osteoporosis. Molecular imaging and immunohistochemistry demonstrated the migration of NIH3T3-G cells from the implantation site throughout the skeleton. In situ analyses revealed coexpression of osteopontin and green fluorescent protein in the newly formed bone tissue, demonstrating that the transplant restored the bone trabecular architecture and mineral density in treated OVX-SAMP8 mice. Interestingly, the life span of OVX-SAMP8 mice receiving PRP/NIH3T3-G transplantation was significantly prolonged and similar to that of the congenic senescence-resistant strain of mice. Conclusion: This unique and yet simple approach could potentially be applied to the treatment of senile postmenopausal osteoporosis and perhaps inborn genetic syndromes associated with accelerated aging, such asHutchinson-Gilford progeria syndrome, and for the prolongation of life expectancy in general.

AB - The aim of this study was to develop a cell-based boneregeneration approach evaluated by molecular imaging and immunohistochemistry. Methods: Genetically modified NIH3T3 embryonic fibroblasts carrying enhanced green fluorescent protein (NIH3T3-G) were predifferentiated into osteoblastlike cells using platelet-rich plasma (PRP) medium, followed by intraosseous transplantation into ovariectomized senescenceaccelerated mouse prone substrain 8 (OVX-SAMP8 mice). Results: PRP-conditioned NIH3T3-G (PRP/NIH3T3-G) engraftment prevented the development of osteoporosis. Molecular imaging and immunohistochemistry demonstrated the migration of NIH3T3-G cells from the implantation site throughout the skeleton. In situ analyses revealed coexpression of osteopontin and green fluorescent protein in the newly formed bone tissue, demonstrating that the transplant restored the bone trabecular architecture and mineral density in treated OVX-SAMP8 mice. Interestingly, the life span of OVX-SAMP8 mice receiving PRP/NIH3T3-G transplantation was significantly prolonged and similar to that of the congenic senescence-resistant strain of mice. Conclusion: This unique and yet simple approach could potentially be applied to the treatment of senile postmenopausal osteoporosis and perhaps inborn genetic syndromes associated with accelerated aging, such asHutchinson-Gilford progeria syndrome, and for the prolongation of life expectancy in general.

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