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Interleukin-18 binding protein transgenic mice are protected against ischemic acute kidney injury


Zhibin, He; Lawrence, Lu; Altmann, Christopher; Hoke, Thomas S.; Ljubanović, Danica; Dinarello, Charles A.; Faubel, Sarah; Edelstein, Charles L.
Interleukin-18 binding protein transgenic mice are protected against ischemic acute kidney injury // American journal of physiology. Renal physiology, 295 (2008), 5; F1414-F1421 doi:10.1152/ajprenal.90288.2008 (međunarodna recenzija, članak, znanstveni)


Naslov
Interleukin-18 binding protein transgenic mice are protected against ischemic acute kidney injury

Autori
Zhibin, He ; Lawrence, Lu ; Altmann, Christopher ; Hoke, Thomas S. ; Ljubanović, Danica ; Dinarello, Charles A. ; Faubel, Sarah ; Edelstein, Charles L.

Izvornik
American journal of physiology. Renal physiology (0363-6127) 295 (2008), 5; F1414-F1421

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Renal chemokines/cytokines

Sažetak
IL-18 function is neutralized in IL-18 binding protein transgenic (IL-18BP Tg) mice. First, we determined whether IL-18BP Tg mice are protected against ischemic acute kidney injury (AKI). Ischemic AKI was induced by bilateral renal pedicle clamping. IL-18BP Tg mice were functionally and histologically protected against ischemic AKI as determined by blood urea nitrogen, serum creatinine, and acute tubular necrosis score. We have demonstrated that the injurious effect of IL-18 in the kidney is independent of neutrophils and lymphocytes. Thus the effect of IL-18 inhibition on renal macrophage infiltration was determined. The number of macrophages was significantly reduced in IL-18BP Tg compared with wild-type kidneys. To determine the cytokines and chemokines that are dependent on IL-18, we performed flow cytometry based assays. Multiple chemokines/cytokines, IL-3, IL-6, IL-15, IL-18, leukemia inhibitory factor, macrophage colony-stimulating factor, macrophage inflammatory protein-2, granulocyte-macrophage colony-stimulating factor, and monocyte chemotactic protein-1 were significantly increased in AKI vs. sham kidneys. Only CXCL1 (also known as KC or IL-8) was significantly increased in AKI vs. sham kidneys and significantly reduced in IL-18BP Tg AKI vs. wild-type AKI kidneys. To determine whether macrophages are the source of CXCL1 in the kidney, we depleted macrophages with liposomal encapsulated clodronate. CXCL1 was significantly decreased in macrophage-depleted vs. control AKI mice. In summary, in ischemic AKI in mice, 1) IL-18BP Tg mice are functionally and histologically protected, 2) macrophage infiltration in the kidney and CXCL1 are significantly reduced in IL-18BP Tg mice, and 3) macrophage depletion significantly reduces CXCL1 in the kidney. In conclusion, protection against ischemic AKI in IL-18BP Tg mice is associated with less macrophage infiltration and less production of CXCL1 in the kidney.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti

Napomena
Rad je kao predavanje prezentiran na skupu ASN 2008 Renal Week, održanom od 06-09.11.2008., Philadelphia, SAD ; objavljen u knjizi sazetaka u casopisu Journal of the American Society of Nephrology. Supplement.



POVEZANOST RADA


Projekt / tema
198-0000000-3355 - Značaj morfoloških čimbenika u dijagnostici, terapiji i prognozi FSGS (Danica Galešić-Ljubanović, )

Ustanove
Medicinski fakultet, Zagreb,
Klinička bolnica "Dubrava"

Autor s matičnim brojem:
Danica Galešić-Ljubanović, (203674)

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • SCI-EXP, SSCI i/ili A&HCI


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