The effects of Omarigliptin on promoting osteoblastic differentiation

Osteoporosis significantly impacts the normal life of the elderly and is reported to be closely related to dysfunction of osteoblastic differentiation. Runt-related transcription factor-2 (Runx2) is a critical transcriptional factor involved in the regulation of osteoblast differentiation. Omariglip...

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Autores principales: Fake Liao, Xiunian Hu, Rijiang Chen
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Lenguaje:EN
Publicado: Taylor & Francis Group 2021
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Acceso en línea:https://doaj.org/article/504331a7a6ad4b2cbadcca6120c029fd
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spelling oai:doaj.org-article:504331a7a6ad4b2cbadcca6120c029fd2021-11-26T11:19:49ZThe effects of Omarigliptin on promoting osteoblastic differentiation2165-59792165-598710.1080/21655979.2021.1999366https://doaj.org/article/504331a7a6ad4b2cbadcca6120c029fd2021-10-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.1999366https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987Osteoporosis significantly impacts the normal life of the elderly and is reported to be closely related to dysfunction of osteoblastic differentiation. Runt-related transcription factor-2 (Runx2) is a critical transcriptional factor involved in the regulation of osteoblast differentiation. Omarigliptin is a novel dipeptidyl peptidase-4 (DDP-4) inhibitor and this study proposes to probe into its possible therapeutic function against Osteoporosis by investigating its impacts on osteoblastic differentiation. Osteogenic medium was used to induce osteoblastic differentiation in MC3T3‑E1 cells, and was verified by the increased alkaline phosphatase (ALP) activity, enhanced mineralization, and promoted expression level of osteoblastic differentiation-related factors, including bone morphogenetic protein-2 (BMP-2), ALP, osteocalcin (Ocn), collagen type I alpha 1 (Col1a1), Collagen Type I alpha 2 (Col1a2), Runx2, osterix (Sp7), fibroblast growth factor receptor 2 (Fgfr2), and fibroblast growth factor receptor 3 (Fgfr3), accompanied by the activation of the p38 and Akt pathways. After treatment with Omarigliptin, the ALP activity and mineralization were further promoted, accompanied by the further upregulation of osteoblastic differentiation-related factors, and activation of the p38 and Akt pathways. Lastly, Omarigliptin-induced osteoblastic differentiation, promoted ALP activity, and increased expression levels of Sp7, Fgfr2, Fgfr3, BMP-2, Ocn, ALP, Col1a1, and Col1a2, in the osteogenic medium- cultured MC3T3‑E1 cells were dramatically abolished by the knockdown of Runx2. Taken together, our data reveal that Omarigliptin promoted osteoblastic differentiation by regulating Runx2.Fake LiaoXiunian HuRijiang ChenTaylor & Francis Grouparticleomarigliptinosteoporosisosteoblastic differentiationrunx2BiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021)
institution DOAJ
collection DOAJ
language EN
topic omarigliptin
osteoporosis
osteoblastic differentiation
runx2
Biotechnology
TP248.13-248.65
spellingShingle omarigliptin
osteoporosis
osteoblastic differentiation
runx2
Biotechnology
TP248.13-248.65
Fake Liao
Xiunian Hu
Rijiang Chen
The effects of Omarigliptin on promoting osteoblastic differentiation
description Osteoporosis significantly impacts the normal life of the elderly and is reported to be closely related to dysfunction of osteoblastic differentiation. Runt-related transcription factor-2 (Runx2) is a critical transcriptional factor involved in the regulation of osteoblast differentiation. Omarigliptin is a novel dipeptidyl peptidase-4 (DDP-4) inhibitor and this study proposes to probe into its possible therapeutic function against Osteoporosis by investigating its impacts on osteoblastic differentiation. Osteogenic medium was used to induce osteoblastic differentiation in MC3T3‑E1 cells, and was verified by the increased alkaline phosphatase (ALP) activity, enhanced mineralization, and promoted expression level of osteoblastic differentiation-related factors, including bone morphogenetic protein-2 (BMP-2), ALP, osteocalcin (Ocn), collagen type I alpha 1 (Col1a1), Collagen Type I alpha 2 (Col1a2), Runx2, osterix (Sp7), fibroblast growth factor receptor 2 (Fgfr2), and fibroblast growth factor receptor 3 (Fgfr3), accompanied by the activation of the p38 and Akt pathways. After treatment with Omarigliptin, the ALP activity and mineralization were further promoted, accompanied by the further upregulation of osteoblastic differentiation-related factors, and activation of the p38 and Akt pathways. Lastly, Omarigliptin-induced osteoblastic differentiation, promoted ALP activity, and increased expression levels of Sp7, Fgfr2, Fgfr3, BMP-2, Ocn, ALP, Col1a1, and Col1a2, in the osteogenic medium- cultured MC3T3‑E1 cells were dramatically abolished by the knockdown of Runx2. Taken together, our data reveal that Omarigliptin promoted osteoblastic differentiation by regulating Runx2.
format article
author Fake Liao
Xiunian Hu
Rijiang Chen
author_facet Fake Liao
Xiunian Hu
Rijiang Chen
author_sort Fake Liao
title The effects of Omarigliptin on promoting osteoblastic differentiation
title_short The effects of Omarigliptin on promoting osteoblastic differentiation
title_full The effects of Omarigliptin on promoting osteoblastic differentiation
title_fullStr The effects of Omarigliptin on promoting osteoblastic differentiation
title_full_unstemmed The effects of Omarigliptin on promoting osteoblastic differentiation
title_sort effects of omarigliptin on promoting osteoblastic differentiation
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/504331a7a6ad4b2cbadcca6120c029fd
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AT rijiangchen theeffectsofomarigliptinonpromotingosteoblasticdifferentiation
AT fakeliao effectsofomarigliptinonpromotingosteoblasticdifferentiation
AT xiunianhu effectsofomarigliptinonpromotingosteoblasticdifferentiation
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