Skip to main content
Top
Published in: BMC Nephrology 1/2019

Open Access 01-12-2019 | Kidney Transplantation | Research article

Urinary nephrospheres indicate recovery from acute kidney injury in renal allograft recipients – a pilot study

Authors: Daniela Knafl, Wolfgang Winnicki, Peter Mazal, Ludwig Wagner

Published in: BMC Nephrology | Issue 1/2019

Login to get access

Abstract

Background

Acute kidney injury represents a major threat to the transplanted kidney. Nevertheless, these kidneys have the potential to fully recover. Tubular regeneration following acute kidney injury is driven by the regenerative potential of tubular cells originating from a tubular stem cell pool. We investigated urinary sediments of acute kidney injury transplanted patients and compared it to those of non-transplanted patients. Thereby we discovered tubular cell agglomerates, which have not been described in vivo. We hypothesized that these so-called nephrospheres were associated with recovery from acute kidney injury.

Methods

Urine sediment of 45 kidney-transplanted and 19 non-transplanted individuals was investigated. Nephrospheres were isolated and stained for several molecular markers including aquaporin 1 (AQP1) and calcium sensing receptor (CASR). Nephrospheres were cultured to examine their growth behavior in vitro. In addition, quantitative PCR for CASR, AQP1, and podocin (NPHS2) was performed.

Results

Nephrospheres were excreted in the urine of 17 kidney-transplant recipients 7 days after onset of acute kidney injury and were detectable over several days until kidney function was recovered to baseline creatinine levels. None were found in the urine of non-transplanted individuals. Nephrospheres were either AQP1+/CASR+ or AQP1−/CASR+ and could be cultured for 27 days. Mitotic cells could still be visualized after 17 days in culture. Quantitative PCR detected AQP1 in both kidney-transplanted and non-transplanted individuals during the phase of creatinine decline. As a limitation qPCR was only performed for the entire urinary sediment.

Conclusions

Nephrospheres are three dimensional tubular cell agglomerates which appeared in urine of kidney transplant recipients recovering from acute kidney injury. Appearance of nephrospheres in urine was independent of the duration after kidney transplantation. Nephrospheres proliferated in cell culture and kept expressing kidney specific marker. Presence of nephrospheres in urine showed a specificity of 100% and a sensitivity of 60.71% for recovery.
Appendix
Available only for authorised users
Literature
1.
go back to reference Peters F, Westphal C, Kramer A, Westerman R. Is the rise in the prevalence of renal replacement therapy at older ages the Price for living longer? Front Public Health. 2018;6:138.CrossRef Peters F, Westphal C, Kramer A, Westerman R. Is the rise in the prevalence of renal replacement therapy at older ages the Price for living longer? Front Public Health. 2018;6:138.CrossRef
2.
go back to reference Ostermann M, Chang RW. Acute kidney injury in the intensive care unit according to RIFLE. Crit Care Med. 2007;35(8):1837–43 quiz 1852.CrossRef Ostermann M, Chang RW. Acute kidney injury in the intensive care unit according to RIFLE. Crit Care Med. 2007;35(8):1837–43 quiz 1852.CrossRef
3.
go back to reference Romagnani P. Of mice and men: the riddle of tubular regeneration. J Pathol. 2013;229(5):641–4.CrossRef Romagnani P. Of mice and men: the riddle of tubular regeneration. J Pathol. 2013;229(5):641–4.CrossRef
4.
go back to reference Bombelli S, Zipeto MA, Torsello B, Bovo G, Di Stefano V, Bugarin C, Zordan P, Vigano P, Cattoretti G, Strada G, et al. PKH(high) cells within clonal human nephrospheres provide a purified adult renal stem cell population. Stem Cell Res. 2013;11(3):1163–77.CrossRef Bombelli S, Zipeto MA, Torsello B, Bovo G, Di Stefano V, Bugarin C, Zordan P, Vigano P, Cattoretti G, Strada G, et al. PKH(high) cells within clonal human nephrospheres provide a purified adult renal stem cell population. Stem Cell Res. 2013;11(3):1163–77.CrossRef
5.
go back to reference Bombelli S, Meregalli C, Scalia C, Bovo G, Torsello B, De Marco S, Cadamuro M, Vigano P, Strada G, Cattoretti G, et al. Nephrosphere-derived cells are induced to multilineage differentiation when cultured on human Decellularized kidney scaffolds. Am J Pathol. 2018;188(1):184–95.CrossRef Bombelli S, Meregalli C, Scalia C, Bovo G, Torsello B, De Marco S, Cadamuro M, Vigano P, Strada G, Cattoretti G, et al. Nephrosphere-derived cells are induced to multilineage differentiation when cultured on human Decellularized kidney scaffolds. Am J Pathol. 2018;188(1):184–95.CrossRef
6.
go back to reference Mantilla JG, Antic T, Tretiakova M. GATA3 as a valuable marker to distinguish clear cell papillary renal cell carcinomas from morphologic mimics. Hum Pathol. 2017;66:152–8.CrossRef Mantilla JG, Antic T, Tretiakova M. GATA3 as a valuable marker to distinguish clear cell papillary renal cell carcinomas from morphologic mimics. Hum Pathol. 2017;66:152–8.CrossRef
7.
go back to reference McCluggage WG, Sumathi VP, Maxwell P. CD10 is a sensitive and diagnostically useful immunohistochemical marker of normal endometrial stroma and of endometrial stromal neoplasms. Histopathology. 2001;39(3):273–8.CrossRef McCluggage WG, Sumathi VP, Maxwell P. CD10 is a sensitive and diagnostically useful immunohistochemical marker of normal endometrial stroma and of endometrial stromal neoplasms. Histopathology. 2001;39(3):273–8.CrossRef
8.
go back to reference Abbaszadeh S, Heidari F. Impact of cold ischemia time on outcome of deceased kidney transplantation. Iran J Kidney Dis. 2012;6(4):229–31.PubMed Abbaszadeh S, Heidari F. Impact of cold ischemia time on outcome of deceased kidney transplantation. Iran J Kidney Dis. 2012;6(4):229–31.PubMed
9.
go back to reference Wieser M, Stadler G, Jennings P, Streubel B, Pfaller W, Ambros P, Riedl C, Katinger H, Grillari J, Grillari-Voglauer R. hTERT alone immortalizes epithelial cells of renal proximal tubules without changing their functional characteristics. Am J Physiol Renal Physiol. 2008;295(5):F1365–75.CrossRef Wieser M, Stadler G, Jennings P, Streubel B, Pfaller W, Ambros P, Riedl C, Katinger H, Grillari J, Grillari-Voglauer R. hTERT alone immortalizes epithelial cells of renal proximal tubules without changing their functional characteristics. Am J Physiol Renal Physiol. 2008;295(5):F1365–75.CrossRef
10.
go back to reference Knafl D, Muller M, Pajenda S, Genc Z, Hecking M, Wagner L. The urine biomarker panel [IGFBP7]x[TIMP-2] (NephroCheck(R) parameter) does not correlate with IGFBP7 and TIMP-2 gene expression in urinary sediment. PLoS One. 2017;12(11):e0188316.CrossRef Knafl D, Muller M, Pajenda S, Genc Z, Hecking M, Wagner L. The urine biomarker panel [IGFBP7]x[TIMP-2] (NephroCheck(R) parameter) does not correlate with IGFBP7 and TIMP-2 gene expression in urinary sediment. PLoS One. 2017;12(11):e0188316.CrossRef
11.
go back to reference Faa G, Gerosa C, Fanni D, Nemolato S, Marinelli V, Locci A, Senes G, Mais V, Van Eyken P, Iacovidou N, et al. CD10 in the developing human kidney: immunoreactivity and possible role in renal embryogenesis. J Matern Fetal Neonatal Med. 2012;25(7):904–11.CrossRef Faa G, Gerosa C, Fanni D, Nemolato S, Marinelli V, Locci A, Senes G, Mais V, Van Eyken P, Iacovidou N, et al. CD10 in the developing human kidney: immunoreactivity and possible role in renal embryogenesis. J Matern Fetal Neonatal Med. 2012;25(7):904–11.CrossRef
12.
go back to reference Tanigawa S, Nishinakamura R. Expanding nephron progenitors in vitro: a step toward regenerative medicine in nephrology. Kidney Int. 2016;90(5):925–7.CrossRef Tanigawa S, Nishinakamura R. Expanding nephron progenitors in vitro: a step toward regenerative medicine in nephrology. Kidney Int. 2016;90(5):925–7.CrossRef
13.
go back to reference Kaminski MM, Tosic J, Kresbach C, Engel H, Klockenbusch J, Muller AL, Pichler R, Grahammer F, Kretz O, Huber TB, et al. Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors. Nat Cell Biol. 2016;18(12):1269–80.CrossRef Kaminski MM, Tosic J, Kresbach C, Engel H, Klockenbusch J, Muller AL, Pichler R, Grahammer F, Kretz O, Huber TB, et al. Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors. Nat Cell Biol. 2016;18(12):1269–80.CrossRef
14.
go back to reference Wyatt CM, Dubois N. In vitro generation of renal tubular epithelial cells from fibroblasts: implications for precision and regenerative medicine in nephrology. Kidney Int. 2017;91(2):265–7.CrossRef Wyatt CM, Dubois N. In vitro generation of renal tubular epithelial cells from fibroblasts: implications for precision and regenerative medicine in nephrology. Kidney Int. 2017;91(2):265–7.CrossRef
15.
go back to reference Ali AS, Al-Shraim M, Al-Hakami AM, Jones IM. Epstein- Barr virus: clinical and epidemiological revisits and genetic basis of oncogenesis. The open virology journal. 2015;9:7–28.CrossRef Ali AS, Al-Shraim M, Al-Hakami AM, Jones IM. Epstein- Barr virus: clinical and epidemiological revisits and genetic basis of oncogenesis. The open virology journal. 2015;9:7–28.CrossRef
Metadata
Title
Urinary nephrospheres indicate recovery from acute kidney injury in renal allograft recipients – a pilot study
Authors
Daniela Knafl
Wolfgang Winnicki
Peter Mazal
Ludwig Wagner
Publication date
01-12-2019

Other articles of this Issue 1/2019

BMC Nephrology 1/2019 Go to the issue