Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Chun, So Young | - |
dc.contributor.author | Kim, Dae Hwan | - |
dc.contributor.author | Kim, Jeong Shik | - |
dc.contributor.author | Kim, Hyun Tae | - |
dc.contributor.author | Yoo, Eun Sang | - |
dc.contributor.author | Chung, Jae-Wook | - |
dc.contributor.author | Ha, Yun-Sok | - |
dc.contributor.author | Song, Phil Hyun | - |
dc.contributor.author | Joung, Yoon Ki | - |
dc.contributor.author | Han, Dong Keun | - |
dc.contributor.author | Chung, Sung Kwang | - |
dc.contributor.author | Kim, Bum Soo | - |
dc.contributor.author | Kwon, Tae Gyun | - |
dc.date.accessioned | 2024-01-19T22:04:18Z | - |
dc.date.available | 2024-01-19T22:04:18Z | - |
dc.date.created | 2021-09-03 | - |
dc.date.issued | 2018-08 | - |
dc.identifier.issn | 1738-2696 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/121119 | - |
dc.description.abstract | Kidney ischemia-reperfusion (IR) via laparotomy is a conventional method for kidney surgery in a mouse model. However, IR, an invasive procedure, can cause serious acute and chronic complications through apoptotic and inflammatory pathways. To avoid these adverse responses, a Non-IR and dorsal slit approach was designed for kidney surgery. Animals were divided into three groups, 1) sham-operated control; 2) IR, Kidney IR via laparotomy; and 3) Non-IR, Non-IR and dorsal slit. The effects of Non-IR method on renal surgery outcomes were verified with respect to animal viability, renal function, apoptosis, inflammation, fibrosis, renal regeneration, and systemic response using histology, immunohistochemistry, real-time polymerase chain reaction, serum chemistry, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining, and Masson's trichrome staining. The Non-IR group showed 100% viability with mild elevation of serum blood urea nitrogen and creatinine values at day 1 after surgery, whereas the IR group showed 20% viability and lethal functional abnormality. Histologically, renal tubule epithelial cell injury was evident on day 1 in the IR group, and cellular apoptosis enhanced TUNEL-positive cell number and Fas/caspase-3 and KIM-1/NGAL expression. Inflammation and fibrosis were high in the IR group, with enhanced CD4/CD8-positive T cell infiltration, inflammatory cytokine secretion, and Masson's trichrome stain-positive cell numbers. The Non-IR group showed a suitable microenvironment for renal regeneration with enhanced host cell migration, reduced immune cell influx, and increased expression of renal differentiation-related genes and anti-inflammatory cytokines. The local renal IR influenced distal organ apoptosis and inflammation by releasing circulating pro-inflammatory cytokines. The Non-IR and dorsal slit method for kidney surgery in a mouse model can be an alternative surgical approach for researchers without adverse reactions such as apoptosis, inflammation, fibrosis, functional impairment, and systemic reactions. | - |
dc.language | English | - |
dc.publisher | KOREAN TISSUE ENGINEERING REGENERATIVE MEDICINE SOC | - |
dc.subject | CELL-DEATH | - |
dc.subject | APOPTOSIS | - |
dc.subject | EXPRESSION | - |
dc.title | A Novel Dorsal Slit Approached Non-Ischemic Partial Nephrectomy Method for a Renal Tissue Regeneration in a Mouse Model | - |
dc.type | Article | - |
dc.identifier.doi | 10.1007/s13770-018-0123-0 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | TISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.15, no.4, pp.453 - 466 | - |
dc.citation.title | TISSUE ENGINEERING AND REGENERATIVE MEDICINE | - |
dc.citation.volume | 15 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 453 | - |
dc.citation.endPage | 466 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
dc.identifier.kciid | ART002371818 | - |
dc.identifier.wosid | 000440200400009 | - |
dc.identifier.scopusid | 2-s2.0-85050534554 | - |
dc.relation.journalWebOfScienceCategory | Cell & Tissue Engineering | - |
dc.relation.journalWebOfScienceCategory | Engineering, Biomedical | - |
dc.relation.journalResearchArea | Cell Biology | - |
dc.relation.journalResearchArea | Engineering | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | CELL-DEATH | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordAuthor | Ischemia-reperfusion | - |
dc.subject.keywordAuthor | Renal regeneration | - |
dc.subject.keywordAuthor | Inflammation | - |
dc.subject.keywordAuthor | Apoptosis | - |
dc.subject.keywordAuthor | Fibrosis | - |
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