Cargando…
Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell
BACKGROUND: Umbilical cord-mesenchymal stem cell-conditioned medium (UC-MSC-CM) has emerged as a promising cell-free therapy. The aim of this study was to explore the therapeutic effects of UC-MSC-CM on insulin resistance in C2C12 cell. METHODS: Insulin resistance was induced by palmitate. Effects o...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Diabetes Association
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024157/ https://www.ncbi.nlm.nih.gov/pubmed/32662257 http://dx.doi.org/10.4093/dmj.2019.0191 |
_version_ | 1783675254003990528 |
---|---|
author | Kim, Kyung-Soo Choi, Yeon Kyung Kim, Mi Jin Hwang, Jung Wook Min, Kyunghoon Jung, Sang Youn Kim, Soo-Kyung Choi, Yong-Soo Cho, Yong-Wook |
author_facet | Kim, Kyung-Soo Choi, Yeon Kyung Kim, Mi Jin Hwang, Jung Wook Min, Kyunghoon Jung, Sang Youn Kim, Soo-Kyung Choi, Yong-Soo Cho, Yong-Wook |
author_sort | Kim, Kyung-Soo |
collection | PubMed |
description | BACKGROUND: Umbilical cord-mesenchymal stem cell-conditioned medium (UC-MSC-CM) has emerged as a promising cell-free therapy. The aim of this study was to explore the therapeutic effects of UC-MSC-CM on insulin resistance in C2C12 cell. METHODS: Insulin resistance was induced by palmitate. Effects of UC-MSC-CM on insulin resistance were evaluated using glucose uptake, glucose transporter type 4 (GLUT4) translocation, the insulin-signaling pathway, and mitochondrial contents and functions in C2C12 cell. RESULTS: Glucose uptake was improved by UC-MSC-CM. UC-MSC-CM treatment increased only in membranous GLUT4 expression, not in cytosolic GLUT4 expression. It restored the insulin-signaling pathway in insulin receptor substrate 1 and protein kinase B. Mitochondrial contents evaluated by mitochondrial transcription factor A, mitochondrial DNA copy number, and peroxisome proliferator-activated receptor gamma coactivator 1-alpha were increased by UC-MSC-CM. In addition, UC-MSC-CM significantly decreased mitochondrial reactive oxygen species and increased fatty acid oxidation and mitochondrial membrane potential. There was no improvement in adenosine triphosphate (ATP) contents, but ATP synthesis was improved by UC-MSC-CM. Cytokine and active factor analysis of UC-MSC-CM showed that it contained many regulators inhibiting insulin resistance. CONCLUSION: UC-MSC-CM improves insulin resistance with multiple mechanisms in C2C12 cell. |
format | Online Article Text |
id | pubmed-8024157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-80241572021-04-14 Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell Kim, Kyung-Soo Choi, Yeon Kyung Kim, Mi Jin Hwang, Jung Wook Min, Kyunghoon Jung, Sang Youn Kim, Soo-Kyung Choi, Yong-Soo Cho, Yong-Wook Diabetes Metab J Original Article BACKGROUND: Umbilical cord-mesenchymal stem cell-conditioned medium (UC-MSC-CM) has emerged as a promising cell-free therapy. The aim of this study was to explore the therapeutic effects of UC-MSC-CM on insulin resistance in C2C12 cell. METHODS: Insulin resistance was induced by palmitate. Effects of UC-MSC-CM on insulin resistance were evaluated using glucose uptake, glucose transporter type 4 (GLUT4) translocation, the insulin-signaling pathway, and mitochondrial contents and functions in C2C12 cell. RESULTS: Glucose uptake was improved by UC-MSC-CM. UC-MSC-CM treatment increased only in membranous GLUT4 expression, not in cytosolic GLUT4 expression. It restored the insulin-signaling pathway in insulin receptor substrate 1 and protein kinase B. Mitochondrial contents evaluated by mitochondrial transcription factor A, mitochondrial DNA copy number, and peroxisome proliferator-activated receptor gamma coactivator 1-alpha were increased by UC-MSC-CM. In addition, UC-MSC-CM significantly decreased mitochondrial reactive oxygen species and increased fatty acid oxidation and mitochondrial membrane potential. There was no improvement in adenosine triphosphate (ATP) contents, but ATP synthesis was improved by UC-MSC-CM. Cytokine and active factor analysis of UC-MSC-CM showed that it contained many regulators inhibiting insulin resistance. CONCLUSION: UC-MSC-CM improves insulin resistance with multiple mechanisms in C2C12 cell. Korean Diabetes Association 2021-03 2020-07-10 /pmc/articles/PMC8024157/ /pubmed/32662257 http://dx.doi.org/10.4093/dmj.2019.0191 Text en Copyright © 2021 Korean Diabetes Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Kyung-Soo Choi, Yeon Kyung Kim, Mi Jin Hwang, Jung Wook Min, Kyunghoon Jung, Sang Youn Kim, Soo-Kyung Choi, Yong-Soo Cho, Yong-Wook Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell |
title | Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell |
title_full | Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell |
title_fullStr | Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell |
title_full_unstemmed | Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell |
title_short | Umbilical Cord-Mesenchymal Stem Cell-Conditioned Medium Improves Insulin Resistance in C2C12 Cell |
title_sort | umbilical cord-mesenchymal stem cell-conditioned medium improves insulin resistance in c2c12 cell |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024157/ https://www.ncbi.nlm.nih.gov/pubmed/32662257 http://dx.doi.org/10.4093/dmj.2019.0191 |
work_keys_str_mv | AT kimkyungsoo umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT choiyeonkyung umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT kimmijin umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT hwangjungwook umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT minkyunghoon umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT jungsangyoun umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT kimsookyung umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT choiyongsoo umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell AT choyongwook umbilicalcordmesenchymalstemcellconditionedmediumimprovesinsulinresistanceinc2c12cell |