Evidence supporting antioxidant action of adipose-derived stem cells: Protection of human dermal fibroblasts from oxidative stress
被引:242
作者:
Kim, Won-Serk
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Prostem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Dermatol, Seoul, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Kim, Won-Serk
[1
,2
]
Park, Byung-Soon
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Prostem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Leaders Clin, Seoul, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Park, Byung-Soon
[1
,3
]
Kim, Hyung-Ki
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Prostem Res Inst, Div Stem Cell Res, Seoul 135010, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Kim, Hyung-Ki
[1
]
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机构:
Park, Jeong-Soo
Kim, Kea-Jeung
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机构:
Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Dermatol, Seoul, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Kim, Kea-Jeung
[2
]
Choi, Joon-Seok
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Dankook Univ, Coll Med, Dept Biochem, Chunan, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Choi, Joon-Seok
[4
]
Chung, Suk-Jae
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Seoul Natl Univ, Coll Pharm, Seoul, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Chung, Suk-Jae
[5
]
Kim, Dae-Duk
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Seoul Natl Univ, Coll Pharm, Seoul, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Kim, Dae-Duk
[5
]
Sung, Jong-Hyuk
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Prostem Res Inst, Div Stem Cell Res, Seoul 135010, South KoreaProstem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
Sung, Jong-Hyuk
[1
]
机构:
[1] Prostem Res Inst, Div Stem Cell Res, Seoul 135010, South Korea
[2] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Dermatol, Seoul, South Korea
[3] Leaders Clin, Seoul, South Korea
[4] Dankook Univ, Coll Med, Dept Biochem, Chunan, South Korea
[5] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
Background: Mesenchymal stem cells within the stromal-vascular fraction of subcutaneous adipose tissue, adipose-derived stem cells (ADSCs), produced soluble factors and they exhibit diverse pharmacological effects in skin biology. Objective: The present study examines the protective effect of ADSCs for human dermal fibroblasts (HDFs) through anti-oxidation in a tert-butyl. hydroperoxide (tbOOH) induced oxidative injury model. Methods and results: The conditioned medium of ADSCs (ADSC-CM) was harvested and tested for antioxidant action. ADSC-CM had an antioxidant effect as potent as 100 mu M ascorbic acid and various antioxidant proteins were detected in ADSC-CM by proteomic analysis. Morphological change and cell survival assay revealed that incubation with ADSC-CM aided HDFs to resist free radicals induced by tbOOH. In addition, activities of superoxide dismutase and glutathione peroxidase were enhanced in the ADSC-CM treated HDFs which confirmed the study hypothesis that ADSCs protect HDFs through antioxidant action. In a cell cycle analysis, ADSC-CM treatment reversed the apoptotic cell death induced by tbOOH and caused a decrease of sub-G1 cells with respect to untreated cells. The anti-apoptotic effect of ADSC-CM was also reproduced by caspase-3 activity assay. Conclusion: These results suggest that ADSCs have potent antioxidant activity and protect HDFs from oxidative injury by decreasing apoptotic cells. Therefore, ADSCS and ADSC-CM are good candidates for control and prevention of skin damage from free radicals in various skin conditions. (c) 2007 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.