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Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells
BACKGROUND/OBJECTIVES: Bone formation and bone resorption continuously occur in bone tissue to prevent the accumulation of old bone, this being called bone remodeling. Osteoblasts especially play a crucial role in bone formation through the differentiation and proliferation. Therefore, in this study...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Nutrition Society and the Korean Society of Community Nutrition
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819124/ https://www.ncbi.nlm.nih.gov/pubmed/27087897 http://dx.doi.org/10.4162/nrp.2016.10.2.148 |
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author | Park, Mi Hwa Kim, Seoyeon Cheon, Jihyeon Lee, Juyeong Kim, Bo Kyung Lee, Sang-Hyeon Kong, Changsuk Kim, Yuck Yong Kim, Mihyang |
author_facet | Park, Mi Hwa Kim, Seoyeon Cheon, Jihyeon Lee, Juyeong Kim, Bo Kyung Lee, Sang-Hyeon Kong, Changsuk Kim, Yuck Yong Kim, Mihyang |
author_sort | Park, Mi Hwa |
collection | PubMed |
description | BACKGROUND/OBJECTIVES: Bone formation and bone resorption continuously occur in bone tissue to prevent the accumulation of old bone, this being called bone remodeling. Osteoblasts especially play a crucial role in bone formation through the differentiation and proliferation. Therefore, in this study, we investigated the effects of Scytosiphon lomentaria extract (SLE) on osteoblastic proliferation and differentiation in MC3T3-E1 cells. MATERIALS/METHODS: A cell proliferation assay, alkaline phosphatase (ALP) activity assay, alizarin red staining and protein expression analysis of osteoblastic genes were carried out to assess the osteoblastic proliferation and differentiation. RESULTS: The results indicated that treatment of SLE promoted the proliferation of MC3T3-E1 cells and improved ALP activity. And, SLE treatment significantly promoted mineralized nodule formation compared with control. In addition, cells treated with SLE significantly upregulated protein expression of ALP, type 1 collagen, bone morphogenetic protein 2, runt-related transcription factor 2, osterix, and osteoprotegerin. CONCLUSIONS: The results demonstrate that SLE promote differentiation inducement and proliferation of osteoblasts and, therefore may help to elucidate the transcriptional mechanism of bone formation and possibly lead to the development of bone-forming drugs. |
format | Online Article Text |
id | pubmed-4819124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Nutrition Society and the Korean Society of Community Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-48191242016-04-15 Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells Park, Mi Hwa Kim, Seoyeon Cheon, Jihyeon Lee, Juyeong Kim, Bo Kyung Lee, Sang-Hyeon Kong, Changsuk Kim, Yuck Yong Kim, Mihyang Nutr Res Pract Original Research BACKGROUND/OBJECTIVES: Bone formation and bone resorption continuously occur in bone tissue to prevent the accumulation of old bone, this being called bone remodeling. Osteoblasts especially play a crucial role in bone formation through the differentiation and proliferation. Therefore, in this study, we investigated the effects of Scytosiphon lomentaria extract (SLE) on osteoblastic proliferation and differentiation in MC3T3-E1 cells. MATERIALS/METHODS: A cell proliferation assay, alkaline phosphatase (ALP) activity assay, alizarin red staining and protein expression analysis of osteoblastic genes were carried out to assess the osteoblastic proliferation and differentiation. RESULTS: The results indicated that treatment of SLE promoted the proliferation of MC3T3-E1 cells and improved ALP activity. And, SLE treatment significantly promoted mineralized nodule formation compared with control. In addition, cells treated with SLE significantly upregulated protein expression of ALP, type 1 collagen, bone morphogenetic protein 2, runt-related transcription factor 2, osterix, and osteoprotegerin. CONCLUSIONS: The results demonstrate that SLE promote differentiation inducement and proliferation of osteoblasts and, therefore may help to elucidate the transcriptional mechanism of bone formation and possibly lead to the development of bone-forming drugs. The Korean Nutrition Society and the Korean Society of Community Nutrition 2016-04 2016-03-02 /pmc/articles/PMC4819124/ /pubmed/27087897 http://dx.doi.org/10.4162/nrp.2016.10.2.148 Text en ©2016 The Korean Nutrition Society and the Korean Society of Community Nutrition 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 Research Park, Mi Hwa Kim, Seoyeon Cheon, Jihyeon Lee, Juyeong Kim, Bo Kyung Lee, Sang-Hyeon Kong, Changsuk Kim, Yuck Yong Kim, Mihyang Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells |
title | Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells |
title_full | Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells |
title_fullStr | Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells |
title_full_unstemmed | Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells |
title_short | Effects of Scytosiphon lomentaria on osteoblastic proliferation and differentiation of MC3T3-E1 cells |
title_sort | effects of scytosiphon lomentaria on osteoblastic proliferation and differentiation of mc3t3-e1 cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4819124/ https://www.ncbi.nlm.nih.gov/pubmed/27087897 http://dx.doi.org/10.4162/nrp.2016.10.2.148 |
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