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Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation
Osteoblasts and osteoclasts play crucial roles in bone formation and bone resorption. We found that plum-derived exosome-like nanovesicles (PENVs) suppressed osteoclast activation and modulated osteoblast differentiation. PENVs increased the proliferation, differentiation, and mineralization of oste...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10180726/ https://www.ncbi.nlm.nih.gov/pubmed/37432256 http://dx.doi.org/10.3390/nu15092107 |
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author | Park, Yu-Seong Kim, Hyun-Woo Hwang, Jin-Hyeon Eom, Jung-Young Kim, Dong-Ha Park, Jinho Tae, Hyun-Jin Lee, Seunghoon Yoo, Jae-Gyu Kim, Jee-In Lim, Jae-Hwan Kwun, In-Sook Baek, Moon-Chang Cho, Young-Eun Kim, Do-Kyun |
author_facet | Park, Yu-Seong Kim, Hyun-Woo Hwang, Jin-Hyeon Eom, Jung-Young Kim, Dong-Ha Park, Jinho Tae, Hyun-Jin Lee, Seunghoon Yoo, Jae-Gyu Kim, Jee-In Lim, Jae-Hwan Kwun, In-Sook Baek, Moon-Chang Cho, Young-Eun Kim, Do-Kyun |
author_sort | Park, Yu-Seong |
collection | PubMed |
description | Osteoblasts and osteoclasts play crucial roles in bone formation and bone resorption. We found that plum-derived exosome-like nanovesicles (PENVs) suppressed osteoclast activation and modulated osteoblast differentiation. PENVs increased the proliferation, differentiation, and mineralization of osteoblastic MC3T3-E1 cells and osteoblasts from mouse bone marrow cultures. Notably, PENVs elevated the expression of osteoblastic transcription factors and osteoblast differentiation marker proteins in MC3T3-E1 cells. Higher levels of phosphorylated BMP-2, p38, JNK, and smad1 proteins were detected in PENV-treated MC3T3-E1 cells. Additionally, the number of TRAP-positive cells was significantly decreased in PENV-treated osteoclasts isolated from osteoblasts from mouse bone marrow cultures. Importantly, osteoclastogenesis of marker proteins such as PPAR-gamma, NFATc1, and c-Fos were suppressed by treatment with PENVs (50 μg/mL). Taken together, these results demonstrate that PENVs can be used as therapeutic targets for treating bone-related diseases by improving osteoblast differentiation and inhibiting osteoclast activation for the first time. |
format | Online Article Text |
id | pubmed-10180726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101807262023-05-13 Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation Park, Yu-Seong Kim, Hyun-Woo Hwang, Jin-Hyeon Eom, Jung-Young Kim, Dong-Ha Park, Jinho Tae, Hyun-Jin Lee, Seunghoon Yoo, Jae-Gyu Kim, Jee-In Lim, Jae-Hwan Kwun, In-Sook Baek, Moon-Chang Cho, Young-Eun Kim, Do-Kyun Nutrients Article Osteoblasts and osteoclasts play crucial roles in bone formation and bone resorption. We found that plum-derived exosome-like nanovesicles (PENVs) suppressed osteoclast activation and modulated osteoblast differentiation. PENVs increased the proliferation, differentiation, and mineralization of osteoblastic MC3T3-E1 cells and osteoblasts from mouse bone marrow cultures. Notably, PENVs elevated the expression of osteoblastic transcription factors and osteoblast differentiation marker proteins in MC3T3-E1 cells. Higher levels of phosphorylated BMP-2, p38, JNK, and smad1 proteins were detected in PENV-treated MC3T3-E1 cells. Additionally, the number of TRAP-positive cells was significantly decreased in PENV-treated osteoclasts isolated from osteoblasts from mouse bone marrow cultures. Importantly, osteoclastogenesis of marker proteins such as PPAR-gamma, NFATc1, and c-Fos were suppressed by treatment with PENVs (50 μg/mL). Taken together, these results demonstrate that PENVs can be used as therapeutic targets for treating bone-related diseases by improving osteoblast differentiation and inhibiting osteoclast activation for the first time. MDPI 2023-04-27 /pmc/articles/PMC10180726/ /pubmed/37432256 http://dx.doi.org/10.3390/nu15092107 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Park, Yu-Seong Kim, Hyun-Woo Hwang, Jin-Hyeon Eom, Jung-Young Kim, Dong-Ha Park, Jinho Tae, Hyun-Jin Lee, Seunghoon Yoo, Jae-Gyu Kim, Jee-In Lim, Jae-Hwan Kwun, In-Sook Baek, Moon-Chang Cho, Young-Eun Kim, Do-Kyun Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation |
title | Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation |
title_full | Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation |
title_fullStr | Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation |
title_full_unstemmed | Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation |
title_short | Plum-Derived Exosome-like Nanovesicles Induce Differentiation of Osteoblasts and Reduction of Osteoclast Activation |
title_sort | plum-derived exosome-like nanovesicles induce differentiation of osteoblasts and reduction of osteoclast activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10180726/ https://www.ncbi.nlm.nih.gov/pubmed/37432256 http://dx.doi.org/10.3390/nu15092107 |
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