Renal Regenerative Capacity Related to Stem Cell Reserve in Nephrectomized Rats

Author:

ARABUL Songul1ORCID,MELIKOGLU Mustafa2ORCID,KIRIMLIOGLU Esma3ORCID,BONEVAL Bezmi Cem1ORCID,KARAGUZEL Gungor1ORCID

Affiliation:

1. Akdeniz University Faculty of Medicine, Departments of Pediatric Surgery

2. 1Akdeniz University Faculty of Medicine, Departments of Pediatric Surgery

3. Akdeniz University Faculty of Medicine, Departments of Histology and Embryology

Abstract

Abstract Purpose: On the new era of stem cell therapy, the present experimental study was conducted to investigate renal regenerative capacity related to kidney stem cell reserve in different nephrectomy (Nx) models. Methods: Three- and eight-week-old rats (n=168) were randomly divided into four groups to include control and three Nx subgroups (1/6 Nx, 1/2 Nx, and 5/6 Nx) (figure 1). On post-Nx days 15, 30 and 60, kidney specimens were obtained to determine renal regenerative capacity. The specimens were examined with immunofluorescence. CD90/CD105 and Ki-67 expressions were determined as stem cell and cellular proliferation markers, respectively. Results: CD90 and CD105 expressions were stronger in glomeruli, but Ki-67 expressions were present only in tubuli. When all Nx types and post-Nx days were considered, both 3- and 8-week-old rats undergone 5/6 Nx had the highest glomerular CD90 and CD105 double expressions. While the expressions gradually increased toward the day 60 in 3-weeks old rats, 8-week-old rats had almost stable double expressions. The strongest tubular Ki-67 expressions were seen in 5/6 Nx groups of both in 3- and 8-week-old rats. The expressions were strongest on day 15 and then gradually decreased. Ipsilateral 1/6 Nx groups had stronger Ki-67 expression than contralateral ones in both age groups. Conclusions: Kidneys may pose a regenerative response to tissue/volume loss through its own CD90- and CD105-related stem cell reserve which mainly takes place in glomeruli and seems to have some interactions with Ki-67-related tubular proliferative process. This response supports that kidney stem cells may have a potential to overcome tissue/volume loss-related damage.

Publisher

Research Square Platform LLC

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5. The monoclonal antibody SH-2, raised against human mesenchymal stem cells, recognizes an epitope on endoglin (CD105);Barry FP;Biochem Biophys Res Commun,1999

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