Cargando…
Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence
The most promising treatment for stress urinary incontinence can be a cell therapy. We suggest human amniotic fluid stem cells (hAFSCs) as an alternative cell source. We established the optimum in vitro protocol for the differentiation from hAFSCs into muscle progenitors. These progenitors were tran...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Medical Sciences
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492662/ https://www.ncbi.nlm.nih.gov/pubmed/23166409 http://dx.doi.org/10.3346/jkms.2012.27.11.1300 |
_version_ | 1782249151585583104 |
---|---|
author | Chun, So Young Cho, Deok Hyun Chae, Seon Yeong Choi, Kyung Hee Lim, Hyun Ju Yoon, Ghil Suk Kim, Bum Soo Kim, Bup Wan Yoo, James J Kwon, Tae Gyun |
author_facet | Chun, So Young Cho, Deok Hyun Chae, Seon Yeong Choi, Kyung Hee Lim, Hyun Ju Yoon, Ghil Suk Kim, Bum Soo Kim, Bup Wan Yoo, James J Kwon, Tae Gyun |
author_sort | Chun, So Young |
collection | PubMed |
description | The most promising treatment for stress urinary incontinence can be a cell therapy. We suggest human amniotic fluid stem cells (hAFSCs) as an alternative cell source. We established the optimum in vitro protocol for the differentiation from hAFSCs into muscle progenitors. These progenitors were transplanted into the injured urethral sphincter and their therapeutic effect was analyzed. For the development of an efficient differentiation system in vitro, we examined a commercial medium, co-culture and conditioned medium (CM) systems. After being treated with CM, hAFSCs were effectively developed into a muscle lineage. The progenitors were integrated into the host urethral sphincter and the host cell differentiation was stimulated in vivo. Urodynamic analysis showed significant increase of leak point pressure and closing pressure. Immunohistochemistry revealed the regeneration of circular muscle mass with normal appearance. Molecular analysis observed the expression of a larger number of target markers. In the immunogenicity analysis, the progenitor group had a scant CD8 lymphocyte. In tumorigenicity, the progenitors showed no teratoma formation. These results suggest that hAFSCs can effectively be differentiated into muscle progenitors in CM and that the hAFSC-derived muscle progenitors are an accessible cell source for the regeneration of injured urethral sphincter. |
format | Online Article Text |
id | pubmed-3492662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-34926622012-11-19 Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence Chun, So Young Cho, Deok Hyun Chae, Seon Yeong Choi, Kyung Hee Lim, Hyun Ju Yoon, Ghil Suk Kim, Bum Soo Kim, Bup Wan Yoo, James J Kwon, Tae Gyun J Korean Med Sci Original Article The most promising treatment for stress urinary incontinence can be a cell therapy. We suggest human amniotic fluid stem cells (hAFSCs) as an alternative cell source. We established the optimum in vitro protocol for the differentiation from hAFSCs into muscle progenitors. These progenitors were transplanted into the injured urethral sphincter and their therapeutic effect was analyzed. For the development of an efficient differentiation system in vitro, we examined a commercial medium, co-culture and conditioned medium (CM) systems. After being treated with CM, hAFSCs were effectively developed into a muscle lineage. The progenitors were integrated into the host urethral sphincter and the host cell differentiation was stimulated in vivo. Urodynamic analysis showed significant increase of leak point pressure and closing pressure. Immunohistochemistry revealed the regeneration of circular muscle mass with normal appearance. Molecular analysis observed the expression of a larger number of target markers. In the immunogenicity analysis, the progenitor group had a scant CD8 lymphocyte. In tumorigenicity, the progenitors showed no teratoma formation. These results suggest that hAFSCs can effectively be differentiated into muscle progenitors in CM and that the hAFSC-derived muscle progenitors are an accessible cell source for the regeneration of injured urethral sphincter. The Korean Academy of Medical Sciences 2012-11 2012-10-30 /pmc/articles/PMC3492662/ /pubmed/23166409 http://dx.doi.org/10.3346/jkms.2012.27.11.1300 Text en © 2012 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Chun, So Young Cho, Deok Hyun Chae, Seon Yeong Choi, Kyung Hee Lim, Hyun Ju Yoon, Ghil Suk Kim, Bum Soo Kim, Bup Wan Yoo, James J Kwon, Tae Gyun Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence |
title | Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence |
title_full | Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence |
title_fullStr | Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence |
title_full_unstemmed | Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence |
title_short | Human Amniotic Fluid Stem Cell-derived Muscle Progenitor Cell Therapy for Stress Urinary Incontinence |
title_sort | human amniotic fluid stem cell-derived muscle progenitor cell therapy for stress urinary incontinence |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492662/ https://www.ncbi.nlm.nih.gov/pubmed/23166409 http://dx.doi.org/10.3346/jkms.2012.27.11.1300 |
work_keys_str_mv | AT chunsoyoung humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT chodeokhyun humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT chaeseonyeong humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT choikyunghee humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT limhyunju humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT yoonghilsuk humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT kimbumsoo humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT kimbupwan humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT yoojamesj humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence AT kwontaegyun humanamnioticfluidstemcellderivedmuscleprogenitorcelltherapyforstressurinaryincontinence |