Matches in SemOpenAlex for { <https://semopenalex.org/work/W2019607092> ?p ?o ?g. }
- W2019607092 endingPage "72" @default.
- W2019607092 startingPage "57" @default.
- W2019607092 abstract "The present study first utilized a standardized shotgun proteomic analysis method to determine differences in protein expression of fibroblasts in the ligament between AS patients and healthy controls. Proteins extracted from primarily cultured FLLs from 35 AS patients and 10 normal subjects were analyzed by automated 2D-Nano-LC-ESI-MS/MS. Differentially expressed proteins were screened by 2-sample t-test and fold change. Bioinformatics analysis of differentially expressed proteins was based on the IPA. Fatty acid β-oxidation-related proteins and INSR pathway-related proteins in the ligament were confirmed by real-time PCR and Western blot. A total of 556 differential proteins were screened in AS. Of them, 322 proteins were up-regulated and the remaining 234 proteins were down-regulated. GO and pathway analyses showed that six fatty acid β-oxidation-related proteins (HADHB, ECHS1, ACSL4, ACADM, ACSL1 and HADH) were up-regulated in FLL cells, which was consistent with the results obtained from real-time PCR, Western blot and MS, while INSR pathway-related proteins (INSR, IRS1, PI3K and PKC) was low in the ligament of AS as compared with that in healthy controls. The lower body fat level in AS maybe due to up-regulation of fatty acid β-oxidation-related enzymes regulated by INSR/PI3K/PKC pathway. Ankylosing spondylitis (AS), a common spondyloarthropathy, is an inflammatory rheumatic disease with a predilection for the axial skeleton. Clinical hallmarks of AS include sacroiliitis, uveitis, enthesitis and persistent spinal inflammation. The pathogenic mechanism of disease causation and perpetuation remains poorly understood. In this study, we primarily cultured fibroblast cells from ligament biopsies, knowing that fibroblast cells are dominant cells in the diseased ligament. One of the characteristic pathologic changes in AS is inflammation of the attachment points, including the muscle, ligament and bone or joint capsule. Inflammation of the tendon attachment point is usually non-bacterial and can lead to pain and swelling of the tendon ligament. To obtain more information, we used Shotgun proteomic analysis based on multidimensional liquid chromatography tandem mass spectrometry (LC-MS/MS). we firstly mixed the lysates of FLL cells derived from the ligaments of 35 AS patients and 10 normal subjects, identified proteins by automated 2D-Nano-LC-ESI-MS/MS method, GO and pathway analyses showed that six fatty acid β-oxidation-related proteins (HADHB, ECHS1, ACSL4, ACADM, ACSL1 and HADH) were up-regulated in the ligament, which was consistent with the results obtained from real-time PCR, Western blot and MS, while INSR pathway-related proteins (INSR, IRS1, PI3K and PKC) was low in the ligament of AS as compared with that in healthy controls. We also find that AS subjects had significantly lower body mass index (BMI) and BMI Z-scores compared with that in healthy controls. The results remind us that up-regulation of fatty acid β-oxidation-related proteins lower the body fat content, which is a new discovery contributing to the progression of AS. This is the first report on fatty acid oxidation in AS. It was found that the body fat level was low in AS due to high fatty acid oxidation, suggesting that insulin signaling may play an important role in the metabolic switch from predominant to fatty acid metabolism that characterizes the ligament of AS. One mechanism for this transition is increased expression of genes that regulate the rate of fatty acid oxidation. This effect may be mediated by PI3K, a downstream mediator of many receptor tyrosine kinases, including the INSR. This is a newly discovered factor contributing to the progression of AS." @default.
- W2019607092 created "2016-06-24" @default.
- W2019607092 creator A5010594394 @default.
- W2019607092 creator A5016664084 @default.
- W2019607092 creator A5027099198 @default.
- W2019607092 creator A5029041901 @default.
- W2019607092 creator A5063652190 @default.
- W2019607092 creator A5063861565 @default.
- W2019607092 creator A5076699095 @default.
- W2019607092 creator A5077188760 @default.
- W2019607092 creator A5078961072 @default.
- W2019607092 creator A5086443370 @default.
- W2019607092 creator A5090988809 @default.
- W2019607092 date "2015-01-01" @default.
- W2019607092 modified "2023-10-01" @default.
- W2019607092 title "Up-regulation of fatty acid oxidation in the ligament as a contributing factor of ankylosing spondylitis: A comparative proteomic study" @default.
- W2019607092 cites W1597678601 @default.
- W2019607092 cites W1964156630 @default.
- W2019607092 cites W1966756689 @default.
- W2019607092 cites W1968878147 @default.
- W2019607092 cites W1987329527 @default.
- W2019607092 cites W2015556811 @default.
- W2019607092 cites W2019260677 @default.
- W2019607092 cites W2049934089 @default.
- W2019607092 cites W2060507266 @default.
- W2019607092 cites W2062019717 @default.
- W2019607092 cites W2062222989 @default.
- W2019607092 cites W2065848419 @default.
- W2019607092 cites W2071383165 @default.
- W2019607092 cites W2086117979 @default.
- W2019607092 cites W2088253044 @default.
- W2019607092 cites W2096880722 @default.
- W2019607092 cites W2100266959 @default.
- W2019607092 cites W2112078820 @default.
- W2019607092 cites W2125503650 @default.
- W2019607092 cites W2134802820 @default.
- W2019607092 cites W2143669749 @default.
- W2019607092 cites W2144377431 @default.
- W2019607092 cites W2152348310 @default.
- W2019607092 cites W2153461957 @default.
- W2019607092 cites W2156459362 @default.
- W2019607092 cites W4210974969 @default.
- W2019607092 cites W4211170289 @default.
- W2019607092 cites W72536532 @default.
- W2019607092 doi "https://doi.org/10.1016/j.jprot.2014.09.014" @default.
- W2019607092 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25281561" @default.
- W2019607092 hasPublicationYear "2015" @default.
- W2019607092 type Work @default.
- W2019607092 sameAs 2019607092 @default.
- W2019607092 citedByCount "16" @default.
- W2019607092 countsByYear W20196070922015 @default.
- W2019607092 countsByYear W20196070922016 @default.
- W2019607092 countsByYear W20196070922017 @default.
- W2019607092 countsByYear W20196070922019 @default.
- W2019607092 countsByYear W20196070922020 @default.
- W2019607092 countsByYear W20196070922022 @default.
- W2019607092 countsByYear W20196070922023 @default.
- W2019607092 crossrefType "journal-article" @default.
- W2019607092 hasAuthorship W2019607092A5010594394 @default.
- W2019607092 hasAuthorship W2019607092A5016664084 @default.
- W2019607092 hasAuthorship W2019607092A5027099198 @default.
- W2019607092 hasAuthorship W2019607092A5029041901 @default.
- W2019607092 hasAuthorship W2019607092A5063652190 @default.
- W2019607092 hasAuthorship W2019607092A5063861565 @default.
- W2019607092 hasAuthorship W2019607092A5076699095 @default.
- W2019607092 hasAuthorship W2019607092A5077188760 @default.
- W2019607092 hasAuthorship W2019607092A5078961072 @default.
- W2019607092 hasAuthorship W2019607092A5086443370 @default.
- W2019607092 hasAuthorship W2019607092A5090988809 @default.
- W2019607092 hasConcept C104317684 @default.
- W2019607092 hasConcept C126322002 @default.
- W2019607092 hasConcept C2776415932 @default.
- W2019607092 hasConcept C2776661782 @default.
- W2019607092 hasConcept C2777402515 @default.
- W2019607092 hasConcept C543025807 @default.
- W2019607092 hasConcept C55493867 @default.
- W2019607092 hasConcept C71924100 @default.
- W2019607092 hasConcept C82714985 @default.
- W2019607092 hasConcept C86803240 @default.
- W2019607092 hasConceptScore W2019607092C104317684 @default.
- W2019607092 hasConceptScore W2019607092C126322002 @default.
- W2019607092 hasConceptScore W2019607092C2776415932 @default.
- W2019607092 hasConceptScore W2019607092C2776661782 @default.
- W2019607092 hasConceptScore W2019607092C2777402515 @default.
- W2019607092 hasConceptScore W2019607092C543025807 @default.
- W2019607092 hasConceptScore W2019607092C55493867 @default.
- W2019607092 hasConceptScore W2019607092C71924100 @default.
- W2019607092 hasConceptScore W2019607092C82714985 @default.
- W2019607092 hasConceptScore W2019607092C86803240 @default.
- W2019607092 hasFunder F4320309612 @default.
- W2019607092 hasFunder F4320321001 @default.
- W2019607092 hasLocation W20196070921 @default.
- W2019607092 hasLocation W20196070922 @default.
- W2019607092 hasOpenAccess W2019607092 @default.
- W2019607092 hasPrimaryLocation W20196070921 @default.
- W2019607092 hasRelatedWork W2102326852 @default.
- W2019607092 hasRelatedWork W2102469932 @default.
- W2019607092 hasRelatedWork W2136599187 @default.