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A cross-sectional study of the role of epithelial cell injury in kidney transplant outcomes
ID
Halloran, Philip F.
(
Avtor
),
ID
Arnol, Miha
(
Avtor
),
ID
Kojc, Nika
(
Avtor
),
ID
Večerić-Haler, Željka
(
Avtor
), et al.
PDF - Predstavitvena datoteka,
prenos
(2,13 MB)
MD5: B7E8761A41F7D1AF506C9ED822F5193A
URL - Izvorni URL, za dostop obiščite
https://insight.jci.org/articles/view/188658
Galerija slik
Izvleček
Background: Expression of acute kidney injury-associated (AKI-associated) transcripts in kidney transplants may reflect recent injury and accumulation of epithelial cells in "failed repair" states. We hypothesized that the phenomenon of failed repair could be associated with deterioration and failure in kidney transplants. Methods: We defined injury-induced transcriptome states in 4,502 kidney transplant biopsies injury-induced gene sets and classifiers previously developed in transplants. Results: In principal component analysis (PCA), PC1 correlated with both acute and chronic kidney injury and related inflammation and PC2 with time posttransplant. Positive PC3 was a dimension that correlated with epithelial remodeling pathways and anticorrelated with inflammation. Both PC1 and PC3 correlated with reduced survival, with PC1 effects strongly increasing over time whereas PC3 effects were independent of time. In this model, we studied the expression of 12 "new" gene sets annotated in single-nucleus RNA-sequencing studies of epithelial cells with failed repair in native kidneys. The new gene sets reflecting epithelial-mesenchymal transition correlated with injury PC1 and PC3, lower estimated glomerular filtration rate, higher donor age, and future failure as strongly as any gene sets previously derived in transplants and were independent of nephron segment of origin and graft rejection. Conclusion: These results suggest 2 dimensions in the kidney transplant response to injury: PC1, AKI-induced changes, failed repair, and inflammation; and PC3, a response involving epithelial remodeling without inflammation. Increasing kidney age amplifies PC1 and PC3.
Jezik:
Angleški jezik
Ključne besede:
molecular diagnosis
,
nephrology
,
organ transplantation
,
transplantation
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2025
Št. strani:
22 str.
Številčenje:
Vol. 10, iss. 10, art. e188658
PID:
20.500.12556/RUL-185582
UDK:
616-07
ISSN pri članku:
2379-3708
COBISS.SI-ID:
238840323
Datum objave v RUL:
11.08.2026
Število ogledov:
230
Število prenosov:
89
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Gradivo je del revije
Naslov:
JCI insight
Skrajšan naslov:
JCI insight
Založnik:
American Society for Clinical Investigtion
ISSN:
2379-3708
COBISS.SI-ID:
56135427
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.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
molekularna diagnoza
,
nefrologija
,
presaditev organov
,
transplantacija
Projekti
Financer:
Genome Canada
Financer:
Canada Foundation for Innovation
Financer:
University of Alberta Hospital Foundation
Financer:
Alberta, Ministry of Advanced Education
Financer:
Mendez National Institute of Transplantation Foundation
Financer:
Industrial Research Assistance Program
Financer:
Thermo Fischer Scientific, One Lambda
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