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Increased L-selectin on monocytes is linked to the autoantibody profile in systemic sclerosis
ID
Brezovec, Neža
(
Avtor
),
ID
Perdan-Pirkmajer, Katja
(
Avtor
),
ID
Kuret, Tadeja
(
Avtor
),
ID
Burja, Blaž
(
Avtor
),
ID
Sodin-Šemrl, Snežna
(
Avtor
),
ID
Čučnik, Saša
(
Avtor
),
ID
Lakota, Katja
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(1,93 MB)
MD5: 2F0E3261DAE12E548D82FF474D2DFE41
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1422-0067/23/4/2233
Galerija slik
Izvleček
Monocytes are known to be implicated in the pathogenesis of systemic sclerosis (SSc), as they exert prominent migratory, adhesive, and chemotactic properties. The aim of our study was to characterize the surface expression of adhesion/chemotactic molecules (CD62L, CD11b, CCR2, CCR5) on the SSc monocytes and determine correlations with the clinical presentation of SSc. We included 38 SSc patients and 36 healthy age-and sex-matched controls. Isolated monocytes, as well as in vitro serum-treated monocytes, were analyzed by flow cytometry; additionally, soluble CD62L was measured in serum. We found increased soluble CD62L in the SSc serum samples and increased CD62L on the surface of the SSc monocytes in the in the same set of patients. Among samples with determined SSc-specific autoantibodies, the surface CD62L was the lowest in patients positive for anti-PM/Scl autoantibodies and the highest in patients with anti-topoisomerase I autoantibodies (ATA). The treatment of isolated healthy monocytes with ATA-positive SSc serum resulted in increased surface CD62L expression. Moreover, surface CCR5 was reduced on the monocytes from SSc patients with interstitial lung disease but also, along with CCR2, negatively correlated with the use of analgesics/anti-inflammatory drugs and immunosuppressants. In conclusion, increased CD62L on SSc monocytes, particularly in ATA-positive patients, provides new insights into the pathogenesis of SSc and suggests CD62L as a potential therapeutic target.
Jezik:
Angleški jezik
Ključne besede:
systemic sclerosis
,
monocytes
,
autoantibodies
,
adhesion
,
chemotaxis
,
CD62L
,
CCR2
,
CCR5
,
CD11b
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2022
Št. strani:
15 str.
Številčenje:
Vol. 23, iss. 4, art. 2233
PID:
20.500.12556/RUL-137285
UDK:
61
ISSN pri članku:
1422-0067
DOI:
10.3390/ijms23042233
COBISS.SI-ID:
98089987
Datum objave v RUL:
09.06.2022
Število ogledov:
843
Število prenosov:
123
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
International journal of molecular sciences
Skrajšan naslov:
Int. j. mol. sci.
Založnik:
MDPI
ISSN:
1422-0067
COBISS.SI-ID:
2779162
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:
17.02.2022
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
sistemska skleroza
,
monociti
,
avtoprotitelesa
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
Z3-9261
Naslov:
Raziskovanje mehanizmov, ki povzročajo fibrozo pri sistemski sklerozi
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
J7-8276
Naslov:
Vpliv protirevmatičnih zdravil na inzulinsko rezistenco in energijsko presnovo v skeletni mišici
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0314
Naslov:
Sistemske avtoimunske bolezni
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