Pregled bibliografske jedinice broj: 1076661
Synovial tissue macrophages are dominantly alternatively activated in patients with mature osteoarthritis
Synovial tissue macrophages are dominantly alternatively activated in patients with mature osteoarthritis // Annals of the Rheumatic Diseases / Smolen, Josef S. (ur.).
London : Delhi: BMJ, 2020. str. 1337-1338 doi:10.1136/annrheumdis-2020-eular.3896 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Synovial tissue macrophages are dominantly
alternatively activated in patients with mature
osteoarthritis
Autori
Laskarin, Gordana ; Kehler, Tatjana ; Legović, Dalen ; Šantić, Veljko ; Ćurko-Cofek, Božena ; Drvar, Vedrana ; Rogoznica, Marija ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Annals of the Rheumatic Diseases
/ Smolen, Josef S. - London : Delhi : BMJ, 2020, 1337-1338
Skup
Annual European Congress of Rheumatology (EULAR 2020)
Mjesto i datum
Frankfurt na Majni, Njemačka; online, 03.06.2020. - 06.06.2020
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Macrophages ; Osteoarthritis ; Synovial membrane ; Arginase-1 ; TNF-alpha
Sažetak
Background: Macrophages are abundant inflammatory cell type in the synovial membrane of knee osteoarthritis (OA). Their quantity is associated with radiographic severity of knee OA and joint symptoms , while their functions are set in response to micro-environmental signals. Classically activated macrophages M1 support T helper 1 (Th1) driven pro- inflammatory reactions, while alternatively activated macrophages M2 strengthen Th2 inflammatory processes. Objectives: To investigate activation status of synovial tissue macrophages in patients with mature OA in terms of M1 / M2 polarization. Methods: Synovial tissue samples (6) with abundant lymphocyte infiltration were obtained during aloarthroplasty. Double immunofluorescence labeling was performed on paraffin-embedded synovial tissue sections using primary rabbit anti-macrophage CD68 mAb in combination with mouse anti-human antibodies directed toward CD3, arginase-1, TNF-alpha and IL-15. CD206 and CD163 were single labelled. Results: CD68+ macrophages mostly co-expressed arginase-1 (4/6 samples), indicating their M2 orientation. Macrophages were placed in lining synovial tissue and nearby tissue-resident CD3+ cells. M2 markers CD206 and CD163 were found in the area of macrophage interaction with T cells. CD68+ cells co-expressing TNF-alpha or IL-15 M1 markers were in minority in these synovial tissues. Lymphocyte infiltration was less abundant in remaining (2/6) synovial tissue samples. Conclusion: Mature synovial tissue macrophages, equipped dominantly with arginase- 1 are M2 oriented and might support Th2 immune response in surrounding T cells.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
Uni-ri-biomed-18- 110
Uni-ri-biomed-18-160
Ustanove:
Medicinski fakultet, Rijeka,
Klinika za ortopediju Lovran,
Akademija medicinskih znanosti,
Klinički bolnički centar Rijeka,
Sveučilište u Rijeci,
Thalassoterapia Opatija,
Fakultet zdravstvenih studija u Rijeci
Profili:
Daniel Rukavina
(autor)
Božena Ćurko-Cofek
(autor)
Gordana Laškarin
(autor)
Veljko Šantić
(autor)
Dalen Legović
(autor)
Tatjana Kehler
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)