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J Am Soc Nephrol. 2016 Aug;27(8):2393-406. doi: 10.1681/ASN.2015060647. Epub 2015 Dec 23.

Severity and Frequency of Proximal Tubule Injury Determines Renal Prognosis.

Author information

1
Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan;
2
Department of Structural Pathology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan;
3
Genome Engineering Technologies and Skeletal Diseases TFA Groups, Regeneron Pharmaceuticals, Inc., Tarrytown, New York;
4
Graduate School of Biological Sciences, Nara Institute of Science and Technology, Nara, Japan;
5
Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan; and.
6
Center for Renal Translational Medicine and Institute of Metabolomic Medicine, Department of Medicine, University of California San Diego, Veteran's Administration San Diego HealthCare System, La Jolla, California.
7
Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan; motoy@kuhp.kyoto-u.ac.jp.

Abstract

AKI increases the risk of developing CKD, but the mechanisms linking AKI to CKD remain unclear. Because proximal tubule injury is the mainstay of AKI, we postulated that proximal tubule injury triggers features of CKD. We generated a novel mouse model to induce proximal tubule-specific adjustable injury by inducing the expression of diphtheria toxin (DT) receptor with variable prevalence in proximal tubules. Administration of high-dose DT in mice expressing the DT receptor consistently caused severe proximal tubule-specific injury associated with interstitial fibrosis and reduction of erythropoietin production. Mild proximal tubule injury from a single injection of low-dose DT triggered reversible fibrosis, whereas repeated mild injuries caused sustained interstitial fibrosis, inflammation, glomerulosclerosis, and atubular glomeruli. DT-induced proximal tubule-specific injury also triggered distal tubule injury. Furthermore, injured tubular cells cocultured with fibroblasts stimulated induction of extracellular matrix and inflammatory genes. These results support the existence of proximal-distal tubule crosstalk and crosstalk between tubular cells and fibroblasts. Overall, our data provide evidence that proximal tubule injury triggers several features of CKD and that the severity and frequency of proximal tubule injury determines the progression to CKD.

KEYWORDS:

acute renal failure; chronic kidney disease; proximal tubule

PMID:
26701981
PMCID:
PMC4978049
DOI:
10.1681/ASN.2015060647
[Indexed for MEDLINE]
Free PMC Article

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