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Status |
Public on Sep 25, 2024 |
Title |
Anti-necroptotic effects of human Wharton’s jelly-derived mesenchymal stem cells in skeletal muscle cell death model via secretion of GRO-α |
Platform organism |
Homo sapiens |
Sample organisms |
Homo sapiens; Mus musculus |
Experiment type |
Protein profiling by protein array
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Summary |
Human mesenchymal stem cells (hMSCs) have therapeutic applications and potential for use in regenerative medicine. However, the use of hMSCs in research and clinical medicine is limited by a lack of information pertaining to their donor-specific functional attributes. In this study, we compared the characteristics of same-donor derived placenta (PL) and Wharton’s jelly (WJ)-derived hMSCs, we also compared their mechanism of action in a skeletal muscle disease in vitro model. The effects of GRO-α were also investigated in a Duchenne muscular dystrophy (DMD) mouse model. The same-donor-derived hWJ- and hPL-MSCs exhibited typical hMSC characteristics. GRO-α was differentially expressed in hWJ- and hPL-MSCs. However, when the secretion of GRO-α was considered, hWJ-MSCs displayed a higher ability to inhibit necroptosis in skeletal muscle cells than hPL-MSCs. This demonstrates the anti-necroptotic therapeutic effect of GRO-α in the skeletal muscle cell death model. Furthermore, considering their potential to inhibit necroptosis in skeletal muscle cells, hWJ-MSCs and the derived GRO-α are novel treatment options for skeletal muscle diseases such as DMD.
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Overall design |
To identify the secreted anti-necroptosis soluble factor from hWJ-MSCs, the conditioned media from each sample group, comprising hWJ- and hPL-MSCs from the same donor co-cultured with C2C12 cells, were analyzed using antibody arrays. We collected the conditioned media from the following groups to perform the array: C2C12 alone, hWJ-MSCs alone (A, B, C), hPL-MSCs alone (A, B, C), and C2C12 cells co-cultured with hWJ-MSCs (A, B, C), or hPL-MSCs (A, B, C). To identify the secreted anti-necroptosis soluble factor from hWJ-MSCs, the conditioned media from each sample group, comprising hWJ- and hPL-MSCs from the same donor co-cultured with C2C12 cells, were analyzed using antibody arrays.
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Contributor(s) |
Park S, Kwon S, Kim S, Jeong J, Kim M, Choi S, Oh S, Ryu G, Jeon H, Chang J |
Citation missing |
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Submission date |
Sep 13, 2024 |
Last update date |
Sep 26, 2024 |
Contact name |
Sun Jeong Kim |
E-mail(s) |
[email protected]
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Phone |
82262058050
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Organization name |
ENCell Co. Ltd.
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Street address |
701, Yeongdong-daero, Gangnam-gu
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City |
Seoul |
ZIP/Postal code |
06072 |
Country |
South Korea |
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Platforms (1) |
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Samples (13)
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GSM8514715 |
medium cultured with hWJ-MSCs_C alone |
GSM8514716 |
medium cultured with hPL-MSCs_A alone |
GSM8514717 |
medium cultured with hPL-MSCs_B alone |
GSM8514718 |
medium cultured with hPL-MSCs_C alone |
GSM8514719 |
medium co-cultured with C2C12 and hWJ-MSCs_A |
GSM8514720 |
medium co-cultured with C2C12 and hWJ-MSCs_B |
GSM8514721 |
medium co-cultured with C2C12 and hWJ-MSCs_C |
GSM8514722 |
medium co-cultured with C2C12 and hPL-MSCs_A |
GSM8514723 |
medium co-cultured with C2C12 and hPL-MSCs_B |
GSM8514724 |
medium co-cultured with C2C12 and hPL-MSCs_C |
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Relations |
BioProject |
PRJNA1160840 |
Supplementary file |
Size |
Download |
File type/resource |
GSE277126_RAW.tar |
580.0 Kb |
(http)(custom) |
TAR (of GPR) |
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