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Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus
BACKGROUND: Diabetes Mellitus (DM), simply known as diabetes, refers to a group of metabolic diseases in which there are high blood sugar levels over a prolonged period. In this study, the feasibility and safety of intravenous transplantation of Very Small Embryonic Like stem cells (VSELs) were inve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Avicenna Research Institute
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388887/ https://www.ncbi.nlm.nih.gov/pubmed/25926949 |
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author | Abouzaripour, Morteza Ragerdi Kashani, Iraj Pasbakhsh, Parichehr Atlasy, Nader |
author_facet | Abouzaripour, Morteza Ragerdi Kashani, Iraj Pasbakhsh, Parichehr Atlasy, Nader |
author_sort | Abouzaripour, Morteza |
collection | PubMed |
description | BACKGROUND: Diabetes Mellitus (DM), simply known as diabetes, refers to a group of metabolic diseases in which there are high blood sugar levels over a prolonged period. In this study, the feasibility and safety of intravenous transplantation of Very Small Embryonic Like stem cells (VSELs) were investigated for diabetes repair, and finally the migration and distribution of these cells in hosts were observed. METHODS: Mouse bone marrow VSELs were isolated by Fluorescent Activating Cell Sorting (FACS) method by using fluorescent antibodies against CD45, CXCR4 and Sca1 markers. Sorted cells were analyzed for expression of oct4 and SSEA1 markers with immunocytochemistry staining method. To determine multilineage differentiation, sorted cells were differentiated to Schwann, osteocyte and beta cells. Ten days after the establishment of a mouse model of pancreas necrosis, DiI-labeled VSELs were injected into these mice via tail vein. Pancreases were harvested 4 weeks after transplantation and the sections of these tissues were observed under fluorescent microscope. RESULTS: It was proved that CD45-, CXCR4+, and Sca1+ sorted cells express oct4 and SSEA1. Our results revealed that intravenously implanted VSELs could migrate into the pancreas of hosts and survive in the diabetic pancreas. In treated groups, blood glucose decreased significantly for at least two month and the weights of mice increased gradually. CONCLUSION: This study provides a strategy for using VSELs for curing diabetes and other regenerative diseases, and the strategy is considered an alternative for other stem cell types. |
format | Online Article Text |
id | pubmed-4388887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Avicenna Research Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-43888872015-04-29 Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus Abouzaripour, Morteza Ragerdi Kashani, Iraj Pasbakhsh, Parichehr Atlasy, Nader Avicenna J Med Biotechnol Original Article BACKGROUND: Diabetes Mellitus (DM), simply known as diabetes, refers to a group of metabolic diseases in which there are high blood sugar levels over a prolonged period. In this study, the feasibility and safety of intravenous transplantation of Very Small Embryonic Like stem cells (VSELs) were investigated for diabetes repair, and finally the migration and distribution of these cells in hosts were observed. METHODS: Mouse bone marrow VSELs were isolated by Fluorescent Activating Cell Sorting (FACS) method by using fluorescent antibodies against CD45, CXCR4 and Sca1 markers. Sorted cells were analyzed for expression of oct4 and SSEA1 markers with immunocytochemistry staining method. To determine multilineage differentiation, sorted cells were differentiated to Schwann, osteocyte and beta cells. Ten days after the establishment of a mouse model of pancreas necrosis, DiI-labeled VSELs were injected into these mice via tail vein. Pancreases were harvested 4 weeks after transplantation and the sections of these tissues were observed under fluorescent microscope. RESULTS: It was proved that CD45-, CXCR4+, and Sca1+ sorted cells express oct4 and SSEA1. Our results revealed that intravenously implanted VSELs could migrate into the pancreas of hosts and survive in the diabetic pancreas. In treated groups, blood glucose decreased significantly for at least two month and the weights of mice increased gradually. CONCLUSION: This study provides a strategy for using VSELs for curing diabetes and other regenerative diseases, and the strategy is considered an alternative for other stem cell types. Avicenna Research Institute 2015 /pmc/articles/PMC4388887/ /pubmed/25926949 Text en Copyright © 2015 Avicenna Research Institute http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Abouzaripour, Morteza Ragerdi Kashani, Iraj Pasbakhsh, Parichehr Atlasy, Nader Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus |
title | Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus |
title_full | Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus |
title_fullStr | Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus |
title_full_unstemmed | Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus |
title_short | Intravenous Transplantation of Very Small Embryonic Like Stem Cells in Treatment of Diabetes Mellitus |
title_sort | intravenous transplantation of very small embryonic like stem cells in treatment of diabetes mellitus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4388887/ https://www.ncbi.nlm.nih.gov/pubmed/25926949 |
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