Cited 40 times in
The third path of tubulointerstitial fibrosis: aberrant endothelial secretome
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 송종욱 | - |
dc.date.accessioned | 2023-08-22T07:17:55Z | - |
dc.date.available | 2023-08-22T07:17:55Z | - |
dc.date.issued | 2017-09 | - |
dc.identifier.issn | 0085-2538 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/196105 | - |
dc.description.abstract | The secretome, defined as a portion of proteins secreted by specific cells to the extracellular space, secures a proper microenvironmental niche not only for the donor cells, but also for the neighboring cells, thus maintaining tissue homeostasis. Communication via secretory products exists between endothelial cells and fibroblasts, and this local mechanism maintains the viability and density of each compartment. Endothelial dysfunction, apart from obvious cell-autonomous defects, leads to the aberrant secretome, which predisposes fibroblasts to acquire a myofibroblastic fibrogenic phenotype. In our recent profiling of the secretome of such dysfunctional profibrogenic renal microvascular endothelial cells, we identified unique profibrogenic signatures, among which we detected ligands of Notch and Wnt-β-catenin pathways. Here, we stress the role of reprogramming cues in the immediate microenvironment of (myo)fibroblasts and the contribution of the endothelial secretome to the panoply of instructive signals in the vicinity of fibroblasts. We hope that this brief overview of endothelial-fibroblast communication in health and disease will lead to eventual unbiased proteomic mapping of individual secretomes of glomerular and tubular epithelial cells, pericytes, and podocytes through reductionist approaches to allow for the synthetic creation of a complex network of secretomic signals acting as reprogramming factors on individual cell types in the kidney. Knowledge of profibrogenic and antifibrogenic signatures in the secretome may garner future therapeutic efforts | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier | - |
dc.relation.isPartOf | KIDNEY INTERNATIONAL | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Cellular Senescence | - |
dc.subject.MESH | Endothelial Cells / metabolism | - |
dc.subject.MESH | Endothelial Cells / pathology* | - |
dc.subject.MESH | Epithelial-Mesenchymal Transition | - |
dc.subject.MESH | Extracellular Space / metabolism | - |
dc.subject.MESH | Fibrosis | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Kidney Tubules / blood supply | - |
dc.subject.MESH | Kidney Tubules / metabolism | - |
dc.subject.MESH | Kidney Tubules / pathology* | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Microvessels / cytology | - |
dc.subject.MESH | Microvessels / metabolism | - |
dc.subject.MESH | Microvessels / pathology* | - |
dc.subject.MESH | Myofibroblasts / metabolism | - |
dc.subject.MESH | Myofibroblasts / pathology* | - |
dc.subject.MESH | Proteome / metabolism* | - |
dc.subject.MESH | Proteomics | - |
dc.subject.MESH | Receptors, Notch / metabolism | - |
dc.subject.MESH | Renal Insufficiency, Chronic / metabolism | - |
dc.subject.MESH | Renal Insufficiency, Chronic / pathology* | - |
dc.subject.MESH | Wnt Proteins / metabolism | - |
dc.subject.MESH | Wnt Signaling Pathway | - |
dc.subject.MESH | beta Catenin / metabolism | - |
dc.title | The third path of tubulointerstitial fibrosis: aberrant endothelial secretome | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Anesthesiology and Pain Medicine (마취통증의학교실) | - |
dc.contributor.googleauthor | Mark Lipphardt | - |
dc.contributor.googleauthor | Jong W Song | - |
dc.contributor.googleauthor | Kei Matsumoto | - |
dc.contributor.googleauthor | Sina Dadafarin | - |
dc.contributor.googleauthor | Hassan Dihazi | - |
dc.contributor.googleauthor | Gerhard Müller | - |
dc.contributor.googleauthor | Michael S Goligorsky | - |
dc.identifier.doi | 10.1016/j.kint.2017.02.033 | - |
dc.contributor.localId | A02060 | - |
dc.relation.journalcode | J01941 | - |
dc.identifier.eissn | 1523-1755 | - |
dc.identifier.pmid | 28476555 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S008525381730176X | - |
dc.subject.keyword | endothelial cell | - |
dc.subject.keyword | fibroblast | - |
dc.subject.keyword | microenvironment | - |
dc.subject.keyword | proteomics | - |
dc.subject.keyword | reprogramming | - |
dc.subject.keyword | secretome | - |
dc.contributor.alternativeName | Song, Jong Wook | - |
dc.contributor.affiliatedAuthor | 송종욱 | - |
dc.citation.volume | 92 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 558 | - |
dc.citation.endPage | 568 | - |
dc.identifier.bibliographicCitation | KIDNEY INTERNATIONAL, Vol.92(3) : 558-568, 2017-09 | - |
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