Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells

Background/purpose: The effect of aspirin on bone regeneration remains controversial. This study aimed to determine the effect of various concentrations of aspirin on cell viability, osteogenic differentiation, cell cycle, and apoptosis on ST2 cells to find an effective range of aspirin for bone reg...

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Main Authors: Mi Du, Wan Pan, Xiaoqi Duan, Pishan Yang, Shaohua Ge
Format: Article
Language:English
Published: Elsevier 2016-09-01
Series:Journal of Dental Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1991790216300174
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spelling doaj-fc62485ce24f4d1793f4d7c5ac48bceb2020-11-24T22:14:47ZengElsevierJournal of Dental Sciences1991-79022016-09-0111331532210.1016/j.jds.2016.03.009Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cellsMi DuWan PanXiaoqi DuanPishan YangShaohua GeBackground/purpose: The effect of aspirin on bone regeneration remains controversial. This study aimed to determine the effect of various concentrations of aspirin on cell viability, osteogenic differentiation, cell cycle, and apoptosis on ST2 cells to find an effective range of aspirin for bone regeneration induction. Materials and methods: Cell viability was measured with MTT assay after being stimulated with aspirin for 1 day, 2 days, 3 days, 5 days, and 7 days. Alkaline phosphatase (ALP) activity was measured after cells were treated for 1 day, 3 days, and 7 days. Expression of runt-related transcription factor 2 (Runx-2) was evaluated using Western-blot analysis at 3 days and 7 days. Flow cytometry was used for cell cycle and apoptosis measurement after cells were treated for 48 hours. Results: Lower concentrations of aspirin (1μΜ and 10μM) promoted cell growth and increased ALP levels and Runx-2 expression, while higher concentrations (100μΜ and 1000μΜ) inhibited cell growth (P < 0.05), and lost their effect on ALP activity after 3 days, while even showing an inhibitory effect on the expression of Runx-2. Aspirin at a concentration of 100μM promoted cell mitosis from the S phase to the G2/M phase, and 1000μM arrested the cell cycle in the resting phase G0/G1 (P < 0.05). Parallel apoptosis/necrosis studies showed the percentage of cells in apoptosis decreased dramatically at any dose of aspirin. Conclusion: A lower dosage of aspirin could promote ST2 cell growth, osteogenic differentiation, and inhibit their apoptosis which indicates that aspirin can be used as an alternative for bone regeneration.http://www.sciencedirect.com/science/article/pii/S1991790216300174apoptosisaspirinbone marrow stromal cellscell cycleosteogenic differentiationproliferation
collection DOAJ
language English
format Article
sources DOAJ
author Mi Du
Wan Pan
Xiaoqi Duan
Pishan Yang
Shaohua Ge
spellingShingle Mi Du
Wan Pan
Xiaoqi Duan
Pishan Yang
Shaohua Ge
Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
Journal of Dental Sciences
apoptosis
aspirin
bone marrow stromal cells
cell cycle
osteogenic differentiation
proliferation
author_facet Mi Du
Wan Pan
Xiaoqi Duan
Pishan Yang
Shaohua Ge
author_sort Mi Du
title Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
title_short Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
title_full Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
title_fullStr Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
title_full_unstemmed Lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
title_sort lower dosage of aspirin promotes cell growth and osteogenic differentiation in murine bone marrow stromal cells
publisher Elsevier
series Journal of Dental Sciences
issn 1991-7902
publishDate 2016-09-01
description Background/purpose: The effect of aspirin on bone regeneration remains controversial. This study aimed to determine the effect of various concentrations of aspirin on cell viability, osteogenic differentiation, cell cycle, and apoptosis on ST2 cells to find an effective range of aspirin for bone regeneration induction. Materials and methods: Cell viability was measured with MTT assay after being stimulated with aspirin for 1 day, 2 days, 3 days, 5 days, and 7 days. Alkaline phosphatase (ALP) activity was measured after cells were treated for 1 day, 3 days, and 7 days. Expression of runt-related transcription factor 2 (Runx-2) was evaluated using Western-blot analysis at 3 days and 7 days. Flow cytometry was used for cell cycle and apoptosis measurement after cells were treated for 48 hours. Results: Lower concentrations of aspirin (1μΜ and 10μM) promoted cell growth and increased ALP levels and Runx-2 expression, while higher concentrations (100μΜ and 1000μΜ) inhibited cell growth (P < 0.05), and lost their effect on ALP activity after 3 days, while even showing an inhibitory effect on the expression of Runx-2. Aspirin at a concentration of 100μM promoted cell mitosis from the S phase to the G2/M phase, and 1000μM arrested the cell cycle in the resting phase G0/G1 (P < 0.05). Parallel apoptosis/necrosis studies showed the percentage of cells in apoptosis decreased dramatically at any dose of aspirin. Conclusion: A lower dosage of aspirin could promote ST2 cell growth, osteogenic differentiation, and inhibit their apoptosis which indicates that aspirin can be used as an alternative for bone regeneration.
topic apoptosis
aspirin
bone marrow stromal cells
cell cycle
osteogenic differentiation
proliferation
url http://www.sciencedirect.com/science/article/pii/S1991790216300174
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AT wanpan lowerdosageofaspirinpromotescellgrowthandosteogenicdifferentiationinmurinebonemarrowstromalcells
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