Cargando…

Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling

Herba Epimedii is a famous Chinese herbal medicine for treating bone diseases. Icariin and icariside II, the main chemical constituents, have attracted great attention from scientists for their potential as antiosteoporosis agents. Our study aimed to evaluate their effects on the lineage commitment...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Dawei, Zhao, Ning, Wan, Chao, Du, Jikun, Lin, Jiantao, Wang, Hongbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702327/
https://www.ncbi.nlm.nih.gov/pubmed/34956384
http://dx.doi.org/10.1155/2021/8069930
_version_ 1784621222160498688
author Zhang, Dawei
Zhao, Ning
Wan, Chao
Du, Jikun
Lin, Jiantao
Wang, Hongbo
author_facet Zhang, Dawei
Zhao, Ning
Wan, Chao
Du, Jikun
Lin, Jiantao
Wang, Hongbo
author_sort Zhang, Dawei
collection PubMed
description Herba Epimedii is a famous Chinese herbal medicine for treating bone diseases. Icariin and icariside II, the main chemical constituents, have attracted great attention from scientists for their potential as antiosteoporosis agents. Our study aimed to evaluate their effects on the lineage commitment of multipotential stromal cells (MSCs). The osteogenesis and adipogenesis of MSCs were assessed by ALP activity, calcium deposition, and adipocyte formation. The expression profiles and levels of osteogenic and adipogenic specific genes were evaluated by cDNA microarray and quantitative real-time PCR. The involvement of extracellular signal-regulated kinase (ERK) signaling was studied by enzyme-linked immunosorbent assay. Icariin and icariside II significantly increased ALP activity and mineralization during osteogenic differentiation of MSCs. Runx2, Col1, and Bmp2 were upregulated in the presence of icariin and icariside II. Meanwhile, they downregulated Pparg, Adipsin, and Cebpb expression during adipogenic differentiation. cDNA microarray revealed 57 differentially expressed genes during lineage commitment of MSCs. In addition, icariin and icariside II enhanced the phosphorylation of ERK, and the above biological effects were blocked by ERK inhibitor U0126. Icariin and icariside II may drive the final lineage commitment of MSCs towards osteogenesis and inhibit adipogenesis through the ERK signaling pathway. Both of them exert multiple osteoprotective effects and deserve more attention for their medicinal and healthcare prospects.
format Online
Article
Text
id pubmed-8702327
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-87023272021-12-24 Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling Zhang, Dawei Zhao, Ning Wan, Chao Du, Jikun Lin, Jiantao Wang, Hongbo Evid Based Complement Alternat Med Research Article Herba Epimedii is a famous Chinese herbal medicine for treating bone diseases. Icariin and icariside II, the main chemical constituents, have attracted great attention from scientists for their potential as antiosteoporosis agents. Our study aimed to evaluate their effects on the lineage commitment of multipotential stromal cells (MSCs). The osteogenesis and adipogenesis of MSCs were assessed by ALP activity, calcium deposition, and adipocyte formation. The expression profiles and levels of osteogenic and adipogenic specific genes were evaluated by cDNA microarray and quantitative real-time PCR. The involvement of extracellular signal-regulated kinase (ERK) signaling was studied by enzyme-linked immunosorbent assay. Icariin and icariside II significantly increased ALP activity and mineralization during osteogenic differentiation of MSCs. Runx2, Col1, and Bmp2 were upregulated in the presence of icariin and icariside II. Meanwhile, they downregulated Pparg, Adipsin, and Cebpb expression during adipogenic differentiation. cDNA microarray revealed 57 differentially expressed genes during lineage commitment of MSCs. In addition, icariin and icariside II enhanced the phosphorylation of ERK, and the above biological effects were blocked by ERK inhibitor U0126. Icariin and icariside II may drive the final lineage commitment of MSCs towards osteogenesis and inhibit adipogenesis through the ERK signaling pathway. Both of them exert multiple osteoprotective effects and deserve more attention for their medicinal and healthcare prospects. Hindawi 2021-12-16 /pmc/articles/PMC8702327/ /pubmed/34956384 http://dx.doi.org/10.1155/2021/8069930 Text en Copyright © 2021 Dawei Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Dawei
Zhao, Ning
Wan, Chao
Du, Jikun
Lin, Jiantao
Wang, Hongbo
Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling
title Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling
title_full Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling
title_fullStr Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling
title_full_unstemmed Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling
title_short Icariin and Icariside II Reciprocally Stimulate Osteogenesis and Inhibit Adipogenesis of Multipotential Stromal Cells through ERK Signaling
title_sort icariin and icariside ii reciprocally stimulate osteogenesis and inhibit adipogenesis of multipotential stromal cells through erk signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702327/
https://www.ncbi.nlm.nih.gov/pubmed/34956384
http://dx.doi.org/10.1155/2021/8069930
work_keys_str_mv AT zhangdawei icariinandicarisideiireciprocallystimulateosteogenesisandinhibitadipogenesisofmultipotentialstromalcellsthrougherksignaling
AT zhaoning icariinandicarisideiireciprocallystimulateosteogenesisandinhibitadipogenesisofmultipotentialstromalcellsthrougherksignaling
AT wanchao icariinandicarisideiireciprocallystimulateosteogenesisandinhibitadipogenesisofmultipotentialstromalcellsthrougherksignaling
AT dujikun icariinandicarisideiireciprocallystimulateosteogenesisandinhibitadipogenesisofmultipotentialstromalcellsthrougherksignaling
AT linjiantao icariinandicarisideiireciprocallystimulateosteogenesisandinhibitadipogenesisofmultipotentialstromalcellsthrougherksignaling
AT wanghongbo icariinandicarisideiireciprocallystimulateosteogenesisandinhibitadipogenesisofmultipotentialstromalcellsthrougherksignaling