Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 강덕희 | * |
| dc.contributor.author | 정성철 | * |
| dc.contributor.author | 조인호 | * |
| dc.date.accessioned | 2025-12-24T16:30:47Z | - |
| dc.date.available | 2025-12-24T16:30:47Z | - |
| dc.date.issued | 2025 | * |
| dc.identifier.issn | 2211-9132 | * |
| dc.identifier.issn | 2211-9140 | * |
| dc.identifier.other | OAK-38375 | * |
| dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/273477 | - |
| dc.description.abstract | Background: Stem cell-based therapy is one of the tools for acute kidney injury (AKI) treatment. Tonsil tissue is a promising alternative source for the high-yield isolation of mesenchymal stem cells (MSCs). This study was undertaken to investigate the effects of tonsil-derived MSCs (T-MSCs) in animal model of AKI induced by gentamicin (GM). Methods: Twenty Sprague-Dawley rats were divided into four groups: Control, GM (70 mg/kg/day, intraperitoneal injection for 10 days), GM + T-MSCs (1 x 107 cells, intravenous injection at 1 day after the last vehicle/GM), and T-MSCs. Renal function, apoptosis, and markers of endoplasmic reticulum stress were measured on day 16 after the first vehicle/GM. Oxidative stress was assessed by measuring urinary 8-hydroxy-2'-deoxyguanosine (8-OHdG) and the expression of glutathione peroxidase (GPx) and catalase. Effects of T-MSCs on GM-induced apoptosis and oxidative stress in NRK cells were also evaluated using a co-culture technique of NRK cells and T-MSC. Results: In the GM + T-MSCs group, blood urea nitrogen, creatinine, and tubular damage score were lower compared to the GM group. T-MSCs injection decreased apoptotic cells and the expression of Bax, cytochrome c, and cleaved caspase and increased Bcl-2. T-MSC injection decreased urinary 8-OHdG and increased expression of GPx and catalase in the kidneys. Anti-human nuclei and PKH26 staining demonstrated the localization of T-MSCs in the tubules of renal cortex. In-vitro study revealed that T-MSCs or T-MSC-conditioned media ameliorated GM-induced nicotinamide adenine dinucleotide phosphate oxidase-1 expression, hydrogen peroxide generation, and apoptosis of NRK cells. Conclusion: Our study demonstrated that T-MSCs ameliorated GM-induced AKI by directly incorporating into the damaged renal tubules and exerting antiapoptotic and antioxidative effects. | * |
| dc.language | English | * |
| dc.publisher | KOREAN SOC NEPHROLOGY | * |
| dc.subject | Acute kidney injury | * |
| dc.subject | Endoplasmic reticulum stress | * |
| dc.subject | Gentamicins | * |
| dc.subject | Oxidative stress | * |
| dc.subject | Tonsil-derived mesenchymal stem cells | * |
| dc.title | Tonsil-derived mesenchymal stem cells protect the kidney from gentamicin-induced acute kidney injury by incorporation into damaged renal tubules and amelioration of oxidative and endoplasmic reticulum stresses | * |
| dc.type | Article | * |
| dc.relation.issue | 6 | * |
| dc.relation.volume | 44 | * |
| dc.relation.index | SCIE | * |
| dc.relation.index | SCOPUS | * |
| dc.relation.index | KCI | * |
| dc.relation.index | KCIE | * |
| dc.relation.startpage | 899 | * |
| dc.relation.lastpage | 915 | * |
| dc.relation.journaltitle | KIDNEY RESEARCH AND CLINICAL PRACTICE | * |
| dc.identifier.doi | 10.23876/j.krcp.24.234 | * |
| dc.identifier.wosid | WOS:001614636600006 | * |
| dc.identifier.scopusid | 2-s2.0-105022429186 | * |
| dc.author.google | Yu, Mina | * |
| dc.author.google | Kim, Dal-Ah | * |
| dc.author.google | Ryu, Eun-Sun | * |
| dc.author.google | Jung, Sung Min | * |
| dc.author.google | Jung, Sung-Chul | * |
| dc.author.google | Jo, Inho | * |
| dc.author.google | Kim, Han Su | * |
| dc.author.google | Kang, Duk-Hee | * |
| dc.contributor.scopusid | 강덕희(17233695600) | * |
| dc.contributor.scopusid | 정성철(57008539100) | * |
| dc.contributor.scopusid | 조인호(26643129000;59283439700) | * |
| dc.date.modifydate | 20260622144939 | * |