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The kidney injury caused by the onset of acute graft-versus-host disease is associated with down-regulation of alpha Klotho
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Antal upphovsmän: 132020 (Engelska)Ingår i: International Immunopharmacology, ISSN 1567-5769, E-ISSN 1878-1705, Vol. 78, artikel-id 106042Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Acute graft-versus-host disease (aGVHD) and kidney injury are the major complications after allogeneic hematopoietic stem cell transplantation (HSCT). Although the underlying mechanisms for the development of these complications are not yet fully understood, it has been proposed that emergence of aGVHD contributes to the development of kidney injury after HSCT. We have shown previously that aGVHD targets the kidney in a biphasic manner: at the onset, inflammatory genes are up-regulated, while when aGVHD becomes established, donor lymphocytes infiltrate the kidney. Here, we characterize renal manifestations at the onset of aGVHD. Mice receiving allogeneic bone marrow and spleen cells displayed symptoms of aGVHD and elevated serum levels of tumor necrosis factor alpha (TNF-alpha) and interferon gamma (IFN-gamma) within 4 days. There was concurrent kidney injury with the following characteristics: (1) elevated expression of the kidney injury biomarker, neutrophil gelatinase-associated lipocalin (NGAL), (2) accumulation of hetero-lysosomes in proximal tubule epithelial cells, and (3) reductions in alpha Klotho mRNA and protein and increased serum levels of fibroblast growth factor 23 (Fgf23), phosphate and urea. This situation resembled acute renal injury caused by bacterial lipopolysaccharide. We conclude that the onset of aGVHD is associated with kidney injury involving down-regulation of alpha Klotho, a sight that may inspire novel therapeutic approaches.

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2020. Vol. 78, artikel-id 106042
Nyckelord [en]
Acute graft versus host disease, Fibroblast growth factor 23, alpha Klotho, Hematopoietic stem cell transplantation, Interferon gamma, Kidney injury, Lysosome, Tumor necrosis factor alpha
Nationell ämneskategori
Immunologi inom det medicinska området Immunologi
Identifikatorer
URN: urn:nbn:se:su:diva-179641DOI: 10.1016/j.intimp.2019.106042ISI: 000510086800002PubMedID: 31812067OAI: oai:DiVA.org:su-179641DiVA, id: diva2:1412578
Tillgänglig från: 2020-03-06 Skapad: 2020-03-06 Senast uppdaterad: 2022-02-26Bibliografiskt granskad

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DePierre, Joseph W.Sadeghi, Behnam

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DePierre, Joseph W.Sadeghi, Behnam
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Institutionen för biokemi och biofysik
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International Immunopharmacology
Immunologi inom det medicinska områdetImmunologi

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