The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney
ABSTRACT Purpose: To identify the fetal stem cell (FSC) response to maternal renal injury with emphasis on renal integrity improvement and Y chromosome detection in damaged maternal kidney. Materials and Methods: Eight non-green fluorescent protein (GFP) transgenic Sprague-Dawley rats were mated w...
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doaj-85e6223be27f4954833d4816cef79d322020-11-25T00:55:44ZengSociedade Brasileira de UrologiaInternational Brazilian Journal of Urology1677-611944360861610.1590/s1677-5538.ibju.2017.0324S1677-55382018000300608The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidneyAbdol-Mohammad KajbafzadehShabnam SabetkishNastaran SabetkishABSTRACT Purpose: To identify the fetal stem cell (FSC) response to maternal renal injury with emphasis on renal integrity improvement and Y chromosome detection in damaged maternal kidney. Materials and Methods: Eight non-green fluorescent protein (GFP) transgenic Sprague-Dawley rats were mated with GFP-positive transgenic male rats. Renal damage was induced on the right kidney at gestational day 11. The same procedure was performed in eight non-pregnant rats as control group. Three months after delivery, right ne- phrectomy was performed in order to evaluate the injured kidney. The fresh perfused kidneys were stained with anti-GFP antibody. Polymerase chain reaction (PCR) assay was also performed for the Y chromosome detection. Cell culture was performed to detect the GFP-positive cells. Technetium-99m-DMSA renal scan and single-photon emission computed tomography (SPECT) were performed after renal damage induction and 3 months later to evaluate the improvement of renal integrity. Results: The presence of FSCs was confirmed by immune histochemical staining as well as immunofluorescent imaging of the damaged part. Gradient PCR of female rat purified DNA demonstrated the presence of Y-chromosome in the damaged maternal kidney. Moreover, the culture of kidney cells showed GPF- positive cells by immuno- fluorescence microscopy. The acute renal scar was repaired and the integrity of dam- aged kidney reached to near normal levels in experimental group as shown in DMSA scan. However, no significant improvement was observed in control group. Conclusion: FSC seems to be the main mechanism in repairing of the maternal renal injury during pregnancy as indicated by Y chromosome and GFP-positive cells in the sub-cultured medium.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382018000300608&lng=en&tlng=enFetal Stem CellsY ChromosomeTechnetium Tc 99m Dimercaptosuccinic AcidGreen Fluorescent Proteins |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Abdol-Mohammad Kajbafzadeh Shabnam Sabetkish Nastaran Sabetkish |
spellingShingle |
Abdol-Mohammad Kajbafzadeh Shabnam Sabetkish Nastaran Sabetkish The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney International Brazilian Journal of Urology Fetal Stem Cells Y Chromosome Technetium Tc 99m Dimercaptosuccinic Acid Green Fluorescent Proteins |
author_facet |
Abdol-Mohammad Kajbafzadeh Shabnam Sabetkish Nastaran Sabetkish |
author_sort |
Abdol-Mohammad Kajbafzadeh |
title |
The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney |
title_short |
The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney |
title_full |
The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney |
title_fullStr |
The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney |
title_full_unstemmed |
The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney |
title_sort |
role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney |
publisher |
Sociedade Brasileira de Urologia |
series |
International Brazilian Journal of Urology |
issn |
1677-6119 |
description |
ABSTRACT Purpose: To identify the fetal stem cell (FSC) response to maternal renal injury with emphasis on renal integrity improvement and Y chromosome detection in damaged maternal kidney. Materials and Methods: Eight non-green fluorescent protein (GFP) transgenic Sprague-Dawley rats were mated with GFP-positive transgenic male rats. Renal damage was induced on the right kidney at gestational day 11. The same procedure was performed in eight non-pregnant rats as control group. Three months after delivery, right ne- phrectomy was performed in order to evaluate the injured kidney. The fresh perfused kidneys were stained with anti-GFP antibody. Polymerase chain reaction (PCR) assay was also performed for the Y chromosome detection. Cell culture was performed to detect the GFP-positive cells. Technetium-99m-DMSA renal scan and single-photon emission computed tomography (SPECT) were performed after renal damage induction and 3 months later to evaluate the improvement of renal integrity. Results: The presence of FSCs was confirmed by immune histochemical staining as well as immunofluorescent imaging of the damaged part. Gradient PCR of female rat purified DNA demonstrated the presence of Y-chromosome in the damaged maternal kidney. Moreover, the culture of kidney cells showed GPF- positive cells by immuno- fluorescence microscopy. The acute renal scar was repaired and the integrity of dam- aged kidney reached to near normal levels in experimental group as shown in DMSA scan. However, no significant improvement was observed in control group. Conclusion: FSC seems to be the main mechanism in repairing of the maternal renal injury during pregnancy as indicated by Y chromosome and GFP-positive cells in the sub-cultured medium. |
topic |
Fetal Stem Cells Y Chromosome Technetium Tc 99m Dimercaptosuccinic Acid Green Fluorescent Proteins |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382018000300608&lng=en&tlng=en |
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