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dc.contributor.authorChun, So Young-
dc.contributor.authorKim, Dae Hwan-
dc.contributor.authorKim, Jeong Shik-
dc.contributor.authorKim, Hyun Tae-
dc.contributor.authorYoo, Eun Sang-
dc.contributor.authorChung, Jae-Wook-
dc.contributor.authorHa, Yun-Sok-
dc.contributor.authorSong, Phil Hyun-
dc.contributor.authorJoung, Yoon Ki-
dc.contributor.authorHan, Dong Keun-
dc.contributor.authorChung, Sung Kwang-
dc.contributor.authorKim, Bum Soo-
dc.contributor.authorKwon, Tae Gyun-
dc.date.accessioned2024-01-19T22:04:18Z-
dc.date.available2024-01-19T22:04:18Z-
dc.date.created2021-09-03-
dc.date.issued2018-08-
dc.identifier.issn1738-2696-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121119-
dc.description.abstractKidney 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.languageEnglish-
dc.publisherKOREAN TISSUE ENGINEERING REGENERATIVE MEDICINE SOC-
dc.subjectCELL-DEATH-
dc.subjectAPOPTOSIS-
dc.subjectEXPRESSION-
dc.titleA Novel Dorsal Slit Approached Non-Ischemic Partial Nephrectomy Method for a Renal Tissue Regeneration in a Mouse Model-
dc.typeArticle-
dc.identifier.doi10.1007/s13770-018-0123-0-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTISSUE ENGINEERING AND REGENERATIVE MEDICINE, v.15, no.4, pp.453 - 466-
dc.citation.titleTISSUE ENGINEERING AND REGENERATIVE MEDICINE-
dc.citation.volume15-
dc.citation.number4-
dc.citation.startPage453-
dc.citation.endPage466-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002371818-
dc.identifier.wosid000440200400009-
dc.identifier.scopusid2-s2.0-85050534554-
dc.relation.journalWebOfScienceCategoryCell & Tissue Engineering-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorIschemia-reperfusion-
dc.subject.keywordAuthorRenal regeneration-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorApoptosis-
dc.subject.keywordAuthorFibrosis-
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KIST Article > 2018
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