The Histopathologic, Pharmacologic and Urodynamic Results of Mesenchymal Stem Cell’s Injection into the Decompensated Rabbit’s Bladder

Objectives We researched the survival of bone marrow-derived mesenchymal stem cells (MSCs) and the results of MSCs’ injected into decompensated bladders in a rabbit model. Methods Partial bladder neck obstruction (PBNO) and subsequent decompensation of the bladder was achieved by wrapping the bladde...

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Veröffentlicht in:Stem cell reviews 2012-12, Vol.8 (4), p.1245-1253
Hauptverfasser: Dayanc, Murat, Kibar, Yusuf, Ural, Ali U., Onguru, Onder, Yildiz, Oguzhan, Irkilata, Hasan C., Avcu, Ferit, Soner, Burak C., Ulku, Cunay, Seyrek, Melik
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container_issue 4
container_start_page 1245
container_title Stem cell reviews
container_volume 8
creator Dayanc, Murat
Kibar, Yusuf
Ural, Ali U.
Onguru, Onder
Yildiz, Oguzhan
Irkilata, Hasan C.
Avcu, Ferit
Soner, Burak C.
Ulku, Cunay
Seyrek, Melik
description Objectives We researched the survival of bone marrow-derived mesenchymal stem cells (MSCs) and the results of MSCs’ injected into decompensated bladders in a rabbit model. Methods Partial bladder neck obstruction (PBNO) and subsequent decompensation of the bladder was achieved by wrapping the bladder neck with autologous rectus fascia. In the first aspect of the experiment 18 rabbits underwent MSC injection into the decompensated bladder to prove the survivability of injected MSCs. For this purpose MSCs were isolated, transfected with Green Fluorescent Protein (GFP), and injected into the detrusor layer. Once viability was assessed in the first phase, an additional 10 rabbits underwent PBNO in the second phase. Five of these animals underwent subsequent MSC injection (group 3, stem cell) and 5 did not (group 2, obstruction). Both groups were compared to 5 controls (group 1). Urodynamics were performed in all groups. After the animals were sacrificed the groups were compared via morphometric analysis, contractile response to carbachol and KCl, and muscarinic receptor type analysis. Results On morphometric analysis, collagenous area rates were 43, 53 and 37 % in group 1, 2 and 3, respectively. There was no statistically significant difference between groups in terms of bladder weight, bladder capacity and vesical pressure. The contractile effects of KCl and muscarinic agonist carbachol were significantly higher in groups 1 and 3 than group 2. The response to carbachol was antagonized by muscarinic M 1 and M 3 receptor antagonist pirenzepine and abolished by muscarinic M 3 receptor antagonist 4-DAMP in all groups. Conclusions The injection of MSCs decreased the collagenous area, increased detrusor contractility. Functional M 3 receptors were also expressed in MSCs-injected bladder smooth muscle as well as in control group.
doi_str_mv 10.1007/s12015-012-9393-4
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Methods Partial bladder neck obstruction (PBNO) and subsequent decompensation of the bladder was achieved by wrapping the bladder neck with autologous rectus fascia. In the first aspect of the experiment 18 rabbits underwent MSC injection into the decompensated bladder to prove the survivability of injected MSCs. For this purpose MSCs were isolated, transfected with Green Fluorescent Protein (GFP), and injected into the detrusor layer. Once viability was assessed in the first phase, an additional 10 rabbits underwent PBNO in the second phase. Five of these animals underwent subsequent MSC injection (group 3, stem cell) and 5 did not (group 2, obstruction). Both groups were compared to 5 controls (group 1). Urodynamics were performed in all groups. After the animals were sacrificed the groups were compared via morphometric analysis, contractile response to carbachol and KCl, and muscarinic receptor type analysis. Results On morphometric analysis, collagenous area rates were 43, 53 and 37 % in group 1, 2 and 3, respectively. There was no statistically significant difference between groups in terms of bladder weight, bladder capacity and vesical pressure. The contractile effects of KCl and muscarinic agonist carbachol were significantly higher in groups 1 and 3 than group 2. The response to carbachol was antagonized by muscarinic M 1 and M 3 receptor antagonist pirenzepine and abolished by muscarinic M 3 receptor antagonist 4-DAMP in all groups. Conclusions The injection of MSCs decreased the collagenous area, increased detrusor contractility. Functional M 3 receptors were also expressed in MSCs-injected bladder smooth muscle as well as in control group.</description><identifier>ISSN: 1550-8943</identifier><identifier>ISSN: 2629-3269</identifier><identifier>EISSN: 1558-6804</identifier><identifier>EISSN: 2629-3277</identifier><identifier>DOI: 10.1007/s12015-012-9393-4</identifier><identifier>PMID: 22736388</identifier><language>eng</language><publisher>New York: Humana Press Inc</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Cell Biology ; Fibrosis ; Life Sciences ; Mesenchymal Stem Cell Transplantation ; Muscle, Smooth - metabolism ; Muscle, Smooth - pathology ; Muscle, Smooth - physiopathology ; Rabbits ; Regenerative Medicine/Tissue Engineering ; Stem Cells ; Transplantation, Homologous ; Urinary Bladder - metabolism ; Urinary Bladder - pathology ; Urinary Bladder - physiopathology ; Urinary Bladder Diseases - metabolism ; Urinary Bladder Diseases - pathology ; Urinary Bladder Diseases - physiopathology ; Urinary Bladder Diseases - therapy ; Urodynamics</subject><ispartof>Stem cell reviews, 2012-12, Vol.8 (4), p.1245-1253</ispartof><rights>Springer Science+Business Media, LLC 2012</rights><rights>Springer Science+Business Media New York 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-4133a1263981ce0585462e2f6dc00b88d6d36fb4eb93695aaf8310d3aed1dfcd3</citedby><cites>FETCH-LOGICAL-c372t-4133a1263981ce0585462e2f6dc00b88d6d36fb4eb93695aaf8310d3aed1dfcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22736388$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dayanc, Murat</creatorcontrib><creatorcontrib>Kibar, Yusuf</creatorcontrib><creatorcontrib>Ural, Ali U.</creatorcontrib><creatorcontrib>Onguru, Onder</creatorcontrib><creatorcontrib>Yildiz, Oguzhan</creatorcontrib><creatorcontrib>Irkilata, Hasan C.</creatorcontrib><creatorcontrib>Avcu, Ferit</creatorcontrib><creatorcontrib>Soner, Burak C.</creatorcontrib><creatorcontrib>Ulku, Cunay</creatorcontrib><creatorcontrib>Seyrek, Melik</creatorcontrib><title>The Histopathologic, Pharmacologic and Urodynamic Results of Mesenchymal Stem Cell’s Injection into the Decompensated Rabbit’s Bladder</title><title>Stem cell reviews</title><addtitle>Stem Cell Rev and Rep</addtitle><addtitle>Stem Cell Rev Rep</addtitle><description>Objectives We researched the survival of bone marrow-derived mesenchymal stem cells (MSCs) and the results of MSCs’ injected into decompensated bladders in a rabbit model. Methods Partial bladder neck obstruction (PBNO) and subsequent decompensation of the bladder was achieved by wrapping the bladder neck with autologous rectus fascia. In the first aspect of the experiment 18 rabbits underwent MSC injection into the decompensated bladder to prove the survivability of injected MSCs. For this purpose MSCs were isolated, transfected with Green Fluorescent Protein (GFP), and injected into the detrusor layer. Once viability was assessed in the first phase, an additional 10 rabbits underwent PBNO in the second phase. Five of these animals underwent subsequent MSC injection (group 3, stem cell) and 5 did not (group 2, obstruction). Both groups were compared to 5 controls (group 1). Urodynamics were performed in all groups. After the animals were sacrificed the groups were compared via morphometric analysis, contractile response to carbachol and KCl, and muscarinic receptor type analysis. Results On morphometric analysis, collagenous area rates were 43, 53 and 37 % in group 1, 2 and 3, respectively. There was no statistically significant difference between groups in terms of bladder weight, bladder capacity and vesical pressure. The contractile effects of KCl and muscarinic agonist carbachol were significantly higher in groups 1 and 3 than group 2. The response to carbachol was antagonized by muscarinic M 1 and M 3 receptor antagonist pirenzepine and abolished by muscarinic M 3 receptor antagonist 4-DAMP in all groups. Conclusions The injection of MSCs decreased the collagenous area, increased detrusor contractility. 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Methods Partial bladder neck obstruction (PBNO) and subsequent decompensation of the bladder was achieved by wrapping the bladder neck with autologous rectus fascia. In the first aspect of the experiment 18 rabbits underwent MSC injection into the decompensated bladder to prove the survivability of injected MSCs. For this purpose MSCs were isolated, transfected with Green Fluorescent Protein (GFP), and injected into the detrusor layer. Once viability was assessed in the first phase, an additional 10 rabbits underwent PBNO in the second phase. Five of these animals underwent subsequent MSC injection (group 3, stem cell) and 5 did not (group 2, obstruction). Both groups were compared to 5 controls (group 1). Urodynamics were performed in all groups. After the animals were sacrificed the groups were compared via morphometric analysis, contractile response to carbachol and KCl, and muscarinic receptor type analysis. Results On morphometric analysis, collagenous area rates were 43, 53 and 37 % in group 1, 2 and 3, respectively. There was no statistically significant difference between groups in terms of bladder weight, bladder capacity and vesical pressure. The contractile effects of KCl and muscarinic agonist carbachol were significantly higher in groups 1 and 3 than group 2. The response to carbachol was antagonized by muscarinic M 1 and M 3 receptor antagonist pirenzepine and abolished by muscarinic M 3 receptor antagonist 4-DAMP in all groups. Conclusions The injection of MSCs decreased the collagenous area, increased detrusor contractility. Functional M 3 receptors were also expressed in MSCs-injected bladder smooth muscle as well as in control group.</abstract><cop>New York</cop><pub>Humana Press Inc</pub><pmid>22736388</pmid><doi>10.1007/s12015-012-9393-4</doi><tpages>9</tpages></addata></record>
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subjects Animals
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Cell Biology
Fibrosis
Life Sciences
Mesenchymal Stem Cell Transplantation
Muscle, Smooth - metabolism
Muscle, Smooth - pathology
Muscle, Smooth - physiopathology
Rabbits
Regenerative Medicine/Tissue Engineering
Stem Cells
Transplantation, Homologous
Urinary Bladder - metabolism
Urinary Bladder - pathology
Urinary Bladder - physiopathology
Urinary Bladder Diseases - metabolism
Urinary Bladder Diseases - pathology
Urinary Bladder Diseases - physiopathology
Urinary Bladder Diseases - therapy
Urodynamics
title The Histopathologic, Pharmacologic and Urodynamic Results of Mesenchymal Stem Cell’s Injection into the Decompensated Rabbit’s Bladder
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