The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney

Detalhes bibliográficos
Autor(a) principal: Kajbafzadeh,Abdol-Mohammad
Data de Publicação: 2018
Outros Autores: Sabetkish,Shabnam, Sabetkish,Nastaran
Tipo de documento: Artigo
Idioma: eng
Título da fonte: International Braz J Urol (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382018000300608
Resumo: 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.
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spelling The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidneyFetal Stem CellsY ChromosomeTechnetium Tc 99m Dimercaptosuccinic AcidGreen Fluorescent ProteinsABSTRACT 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.Sociedade Brasileira de Urologia2018-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382018000300608International braz j urol v.44 n.3 2018reponame:International Braz J Urol (Online)instname:Sociedade Brasileira de Urologia (SBU)instacron:SBU10.1590/s1677-5538.ibju.2017.0324info:eu-repo/semantics/openAccessKajbafzadeh,Abdol-MohammadSabetkish,ShabnamSabetkish,Nastaraneng2018-06-22T00:00:00Zoai:scielo:S1677-55382018000300608Revistahttp://www.brazjurol.com.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||brazjurol@brazjurol.com.br1677-61191677-5538opendoar:2018-06-22T00:00International Braz J Urol (Online) - Sociedade Brasileira de Urologia (SBU)false
dc.title.none.fl_str_mv The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney
title The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney
spellingShingle The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney
Kajbafzadeh,Abdol-Mohammad
Fetal Stem Cells
Y Chromosome
Technetium Tc 99m Dimercaptosuccinic Acid
Green Fluorescent Proteins
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 The role of fetal-maternal microchimerism as a natural-born healer in integrity improvement of maternal damaged kidney
author Kajbafzadeh,Abdol-Mohammad
author_facet Kajbafzadeh,Abdol-Mohammad
Sabetkish,Shabnam
Sabetkish,Nastaran
author_role author
author2 Sabetkish,Shabnam
Sabetkish,Nastaran
author2_role author
author
dc.contributor.author.fl_str_mv Kajbafzadeh,Abdol-Mohammad
Sabetkish,Shabnam
Sabetkish,Nastaran
dc.subject.por.fl_str_mv Fetal Stem Cells
Y Chromosome
Technetium Tc 99m Dimercaptosuccinic Acid
Green Fluorescent Proteins
topic Fetal Stem Cells
Y Chromosome
Technetium Tc 99m Dimercaptosuccinic Acid
Green Fluorescent Proteins
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.
publishDate 2018
dc.date.none.fl_str_mv 2018-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382018000300608
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/s1677-5538.ibju.2017.0324
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Urologia
publisher.none.fl_str_mv Sociedade Brasileira de Urologia
dc.source.none.fl_str_mv International braz j urol v.44 n.3 2018
reponame:International Braz J Urol (Online)
instname:Sociedade Brasileira de Urologia (SBU)
instacron:SBU
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reponame_str International Braz J Urol (Online)
collection International Braz J Urol (Online)
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