The Angiogenic Capacity From Ligamentum Flavum Subsequent to Inflammation A Critical Component of the Pathomechanism of Hypertrophy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Moon, Hong Joo | - |
dc.contributor.author | Park, Youn-Kwan | - |
dc.contributor.author | Ryu, Youngjoon | - |
dc.contributor.author | Kim, Jong-Hyun | - |
dc.contributor.author | Kwon, Taek-Hyun | - |
dc.contributor.author | Chung, Hung-Seob | - |
dc.contributor.author | Kim, Joo Han | - |
dc.date.accessioned | 2021-09-06T10:17:08Z | - |
dc.date.available | 2021-09-06T10:17:08Z | - |
dc.date.created | 2021-06-19 | - |
dc.date.issued | 2012-02-01 | - |
dc.identifier.issn | 0362-2436 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/106082 | - |
dc.description.abstract | Study Design. In vitro study about angiogenic potentiality of ligamentum flavum (LF) cells using coculture of human lumbar LF cells and activated macropage-like THP-1 cells. Objective. To test our hypothesis that activated LF, which was exposed to inflammation, induces angiogenesis, thus resulting in hypertrophy. Summary of Background Data. Inflammatory reactions after mechanical stress produce fibrosis and scarring of the LF that result in hypertrophy, a major pathological feature of spinal stenosis. This study evaluated the roles of LF cells in the pathomechanism of hypertrophy, focusing on angiogenesis. Methods. To determine their response to the inflammatory reaction, human LF cells were cocultured with phorbol myristate acetate-stimulated macrophage-like THP-1 cells. The conditioned media were assayed for tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-6, IL-8, vascular endothelial growth factor (VEGF), and transforming growth factor (TGF)-beta 1. Naive and macrophage-exposed LF cells that responded to TNF-alpha/IL-1 beta were compared using the same outcome measures. Hypertrophied LF tissue was stained by TGF-beta 1 primary antibody using immunohistochemical method. Results. Larger quantities of IL-6, IL-8, and VEGF were secreted by cocultured cells than by macrophages alone and LF cells alone combined. Prior macrophage exposure increased the secretion of IL-8 and VEGF in response to TNF-alpha/IL-1 beta stimulation whereas IL-6 production was increased in response to IL-1 beta. The coculture appeared to increase TGF-beta 1 secretion but the level was lower than that for macrophage-like cells alone and LF cells alone combined. Conclusion. LF cells interact with macrophage-like cells to produce angiogenesis-related factors except TGF-beta 1. Activated LF cells that have been exposed to macrophage, can impact the inducement of angiogenesis-related factors, suggesting that fibrosis and scarring during inflammatory reaction is the major pathomechanism of LF hypertrophy. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | LIPPINCOTT WILLIAMS & WILKINS | - |
dc.subject | ENDOTHELIAL-GROWTH-FACTOR | - |
dc.subject | LUMBAR SPINAL STENOSIS | - |
dc.subject | CANAL STENOSIS | - |
dc.subject | THP-1 CELLS | - |
dc.subject | IN-VITRO | - |
dc.subject | TGF-BETA | - |
dc.subject | INDUCTION | - |
dc.subject | REPAIR | - |
dc.subject | EXPRESSION | - |
dc.subject | FIBROSIS | - |
dc.title | The Angiogenic Capacity From Ligamentum Flavum Subsequent to Inflammation A Critical Component of the Pathomechanism of Hypertrophy | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Park, Youn-Kwan | - |
dc.contributor.affiliatedAuthor | Kim, Jong-Hyun | - |
dc.contributor.affiliatedAuthor | Kwon, Taek-Hyun | - |
dc.contributor.affiliatedAuthor | Chung, Hung-Seob | - |
dc.contributor.affiliatedAuthor | Kim, Joo Han | - |
dc.identifier.doi | 10.1097/BRS.0b013e3182269b19 | - |
dc.identifier.scopusid | 2-s2.0-84856692467 | - |
dc.identifier.wosid | 000300227300002 | - |
dc.identifier.bibliographicCitation | SPINE, v.37, no.3, pp.E147 - E155 | - |
dc.relation.isPartOf | SPINE | - |
dc.citation.title | SPINE | - |
dc.citation.volume | 37 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | E147 | - |
dc.citation.endPage | E155 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.relation.journalResearchArea | Orthopedics | - |
dc.relation.journalWebOfScienceCategory | Clinical Neurology | - |
dc.relation.journalWebOfScienceCategory | Orthopedics | - |
dc.subject.keywordPlus | ENDOTHELIAL-GROWTH-FACTOR | - |
dc.subject.keywordPlus | LUMBAR SPINAL STENOSIS | - |
dc.subject.keywordPlus | CANAL STENOSIS | - |
dc.subject.keywordPlus | THP-1 CELLS | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | TGF-BETA | - |
dc.subject.keywordPlus | INDUCTION | - |
dc.subject.keywordPlus | REPAIR | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.subject.keywordPlus | FIBROSIS | - |
dc.subject.keywordAuthor | angiogenesis | - |
dc.subject.keywordAuthor | human monocytic THP-1 cell line | - |
dc.subject.keywordAuthor | hypertrophy | - |
dc.subject.keywordAuthor | inflammation | - |
dc.subject.keywordAuthor | ligamentum flavum | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
(02841) 서울특별시 성북구 안암로 14502-3290-1114
COPYRIGHT © 2021 Korea University. All Rights Reserved.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.