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Urinary extracellular vesicles and their miRNA cargo in patients with Fabry nephropathy
ID
Levstek, Tina
(
Avtor
),
ID
Mlinšek, Teo
(
Avtor
),
ID
Holcar, Marija
(
Avtor
),
ID
Goričar, Katja
(
Avtor
),
ID
Lenassi, Metka
(
Avtor
),
ID
Dolžan, Vita
(
Avtor
),
ID
Vujkovac, Bojan
(
Avtor
),
ID
Trebušak Podkrajšek, Katarina
(
Avtor
)
PDF - Predstavitvena datoteka,
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MD5: 5E2A8DBBBEA0907EFA7CC4A7477835E5
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/2073-4425/12/7/1057
Galerija slik
Izvleček
Current biomarkers of Fabry nephropathy lack sensitivity in detecting early kidney damage and do not predict progression of nephropathy. Urinary extracellular vesicles (uEVs) and their molecular cargo could reflect early changes in renal impairment as they are secreted by the cells lining the urinary tract. We aimed to conduct a proof-of-concept study to investigate whether analysis of uEV characteristics and expression of uEV-derived microRNAs (miRNAs) could be applicable in studies to predict the development and progression of nephropathy in Fabry disease. A total of 20 Fabry patients were divided into two groups, depending on the presence of nephropathy. Chronological urine samples collected during 10-year follow-up were used for uEVs isolation with size exclusion chromatography. Nanoparticle tracking analysis was used to determine concentration and size of uEVs. We evaluated the expression of five uEV-derived miRNAs by qPCR (miR-23a-3p, miR-29a-3p, miR-30b-5p, miR-34a-5p, miR-200a-3p). There was no difference in the concentration and size of uEVs between patients with and without nephropathy at last follow-up or longitudinally. However, we found increased expression of miR-29a-3p and miR-200a-3p in uEVs isolated from chronological samples of patients with Fabry nephropathy. This may indicate an attempt by the organism to prevent the progression of renal damage leading to end-stage renal disease as previously reported in type 1 diabetes. In addition, we found an increased expression of miR-30b-5p in the 10-year period in uEVs of patients without renal dysfunction. miR-30b-5 was reported to have a protective role in podocyte injury and may possibly be important in Fabry nephropathy. These findings indicate that uEVs and their molecular cargo could be a promising target of studies focusing on elucidation of Fabry nephropathy. Nevertheless, total concentration and size of uEVs were neither indicative of the presence nor progression of Fabry nephropathy, while the role of the analyzed miRNAs in Fabry nephropathy progression was merely indicated and needs further in-depth studies.
Jezik:
Angleški jezik
Ključne besede:
Fabry nephropathy
,
urinary extracellular vesicles
,
miRNA expression
,
biomarker
,
NTA
,
Fabry disease
,
lysosomal storage disease
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2021
Št. strani:
15 str.
Številčenje:
Vol. 12, iss. 7, art. 1057
PID:
20.500.12556/RUL-135603
UDK:
616.6
ISSN pri članku:
2073-4425
DOI:
10.3390/genes12071057
COBISS.SI-ID:
70049795
Datum objave v RUL:
22.03.2022
Število ogledov:
1355
Število prenosov:
132
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Genes
Skrajšan naslov:
Genes
Založnik:
Multidisciplinary Digital Publishing Institute (MDPI)
ISSN:
2073-4425
COBISS.SI-ID:
523100185
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:
09.07.2021
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
Fabryjeva nefropatija
,
urinski zunajcelični vezikli
,
izražanje miRNA
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P1-0170
Naslov:
Molekulski mehanizmi uravnavanja celičnih procesov v povezavi z nekaterimi boleznimi pri človeku
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Sanofi Aventis
Številka projekta:
15-209 FCA
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