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Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells

BACKGROUND: Lymphedema is one of the serious clinical problems that can occur after surgical resection of malignant tumors such as breast cancer or intra‐pelvic cancers. However, no effective treatment options exist at present. Here, we report that implantation of adipose‐derived regenerative cells...

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Autores principales: Shimizu, Yuuki, Shibata, Rei, Shintani, Satoshi, Ishii, Masakazu, Murohara, Toyoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487362/
https://www.ncbi.nlm.nih.gov/pubmed/23130156
http://dx.doi.org/10.1161/JAHA.112.000877
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author Shimizu, Yuuki
Shibata, Rei
Shintani, Satoshi
Ishii, Masakazu
Murohara, Toyoaki
author_facet Shimizu, Yuuki
Shibata, Rei
Shintani, Satoshi
Ishii, Masakazu
Murohara, Toyoaki
author_sort Shimizu, Yuuki
collection PubMed
description BACKGROUND: Lymphedema is one of the serious clinical problems that can occur after surgical resection of malignant tumors such as breast cancer or intra‐pelvic cancers. However, no effective treatment options exist at present. Here, we report that implantation of adipose‐derived regenerative cells (ADRCs) can induce lymphangiogenesis in a mouse model of reparative lymphedema. METHODS AND RESULTS: ADRCs were isolated from C57BL/6J mice. To examine the therapeutic efficacy of ADRC implantation in vivo, we established a new mouse model of tail lymphedema. Lymphedema was improved significantly by local injection of ADRCs (P<0.05). Histological analysis revealed that lymphatic capillary density was greater in the ADRC group than in the phosphate‐buffered saline control group (P<0.01). Tissue expression of vascular endothelial growth factor C mRNA and plasma levels of vascular endothelial growth factor C were greater in the ADRC group than in the control group (P<0.01 and P<0.05, respectively). ADRCs released vascular endothelial growth factor C, which directly stimulated lymphangiogenesis. Implantation of ADRCs also enhanced recruitment of bone marrow–derived M2 macrophages, which served as lymphatic endothelial progenitor cells. CONCLUSIONS: Implantation of autologous ADRCs could be a useful treatment option for patients with severe lymphedema via mediation of lymphangiogenesis. (J Am Heart Assoc. 2012;1:e000877 doi: 10.1161/JAHA.112.000877.)
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spelling pubmed-34873622012-11-03 Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells Shimizu, Yuuki Shibata, Rei Shintani, Satoshi Ishii, Masakazu Murohara, Toyoaki J Am Heart Assoc Original Research BACKGROUND: Lymphedema is one of the serious clinical problems that can occur after surgical resection of malignant tumors such as breast cancer or intra‐pelvic cancers. However, no effective treatment options exist at present. Here, we report that implantation of adipose‐derived regenerative cells (ADRCs) can induce lymphangiogenesis in a mouse model of reparative lymphedema. METHODS AND RESULTS: ADRCs were isolated from C57BL/6J mice. To examine the therapeutic efficacy of ADRC implantation in vivo, we established a new mouse model of tail lymphedema. Lymphedema was improved significantly by local injection of ADRCs (P<0.05). Histological analysis revealed that lymphatic capillary density was greater in the ADRC group than in the phosphate‐buffered saline control group (P<0.01). Tissue expression of vascular endothelial growth factor C mRNA and plasma levels of vascular endothelial growth factor C were greater in the ADRC group than in the control group (P<0.01 and P<0.05, respectively). ADRCs released vascular endothelial growth factor C, which directly stimulated lymphangiogenesis. Implantation of ADRCs also enhanced recruitment of bone marrow–derived M2 macrophages, which served as lymphatic endothelial progenitor cells. CONCLUSIONS: Implantation of autologous ADRCs could be a useful treatment option for patients with severe lymphedema via mediation of lymphangiogenesis. (J Am Heart Assoc. 2012;1:e000877 doi: 10.1161/JAHA.112.000877.) Blackwell Publishing Ltd 2012-08-24 /pmc/articles/PMC3487362/ /pubmed/23130156 http://dx.doi.org/10.1161/JAHA.112.000877 Text en © 2012 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley-Blackwell. http://creativecommons.org/licenses/by/2.5/ This is an Open Access article under the terms of the Creative Commons Attribution Noncommercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Shimizu, Yuuki
Shibata, Rei
Shintani, Satoshi
Ishii, Masakazu
Murohara, Toyoaki
Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells
title Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells
title_full Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells
title_fullStr Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells
title_full_unstemmed Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells
title_short Therapeutic Lymphangiogenesis With Implantation of Adipose‐Derived Regenerative Cells
title_sort therapeutic lymphangiogenesis with implantation of adipose‐derived regenerative cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487362/
https://www.ncbi.nlm.nih.gov/pubmed/23130156
http://dx.doi.org/10.1161/JAHA.112.000877
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