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SP1 regulates BMSC osteogenic differentiation through the miR-133a-3p/MAPK3 axis
by
Wang, Cong
, Zhong, Liying
, Ru, Wenjuan
, Liu, Runzhi
, Zhong, Aimin
, Xiong, Ting
, Li, Shundong
, Sun, Yehai
, Dai, Wei
in
Animals
/ Cell Differentiation - genetics
/ Cell Differentiation - physiology
/ Cells, Cultured
/ Disease Models, Animal
/ Male
/ Medicine
/ Medicine & Public Health
/ Mesenchymal Stem Cells - metabolism
/ Mice
/ Mice, Inbred BALB C
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Mitogen-Activated Protein Kinase 3 - genetics
/ Mitogen-Activated Protein Kinase 3 - metabolism
/ Orthopedics
/ Osteogenesis - genetics
/ Osteogenesis - physiology
/ Osteoporosis - genetics
/ Osteoporosis - metabolism
/ Osteoporosis - pathology
/ Research Article
/ Sp1 Transcription Factor - genetics
/ Sp1 Transcription Factor - metabolism
/ Surgical Orthopedics
2024
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SP1 regulates BMSC osteogenic differentiation through the miR-133a-3p/MAPK3 axis
by
Wang, Cong
, Zhong, Liying
, Ru, Wenjuan
, Liu, Runzhi
, Zhong, Aimin
, Xiong, Ting
, Li, Shundong
, Sun, Yehai
, Dai, Wei
in
Animals
/ Cell Differentiation - genetics
/ Cell Differentiation - physiology
/ Cells, Cultured
/ Disease Models, Animal
/ Male
/ Medicine
/ Medicine & Public Health
/ Mesenchymal Stem Cells - metabolism
/ Mice
/ Mice, Inbred BALB C
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Mitogen-Activated Protein Kinase 3 - genetics
/ Mitogen-Activated Protein Kinase 3 - metabolism
/ Orthopedics
/ Osteogenesis - genetics
/ Osteogenesis - physiology
/ Osteoporosis - genetics
/ Osteoporosis - metabolism
/ Osteoporosis - pathology
/ Research Article
/ Sp1 Transcription Factor - genetics
/ Sp1 Transcription Factor - metabolism
/ Surgical Orthopedics
2024
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SP1 regulates BMSC osteogenic differentiation through the miR-133a-3p/MAPK3 axis
by
Wang, Cong
, Zhong, Liying
, Ru, Wenjuan
, Liu, Runzhi
, Zhong, Aimin
, Xiong, Ting
, Li, Shundong
, Sun, Yehai
, Dai, Wei
in
Animals
/ Cell Differentiation - genetics
/ Cell Differentiation - physiology
/ Cells, Cultured
/ Disease Models, Animal
/ Male
/ Medicine
/ Medicine & Public Health
/ Mesenchymal Stem Cells - metabolism
/ Mice
/ Mice, Inbred BALB C
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ Mitogen-Activated Protein Kinase 3 - genetics
/ Mitogen-Activated Protein Kinase 3 - metabolism
/ Orthopedics
/ Osteogenesis - genetics
/ Osteogenesis - physiology
/ Osteoporosis - genetics
/ Osteoporosis - metabolism
/ Osteoporosis - pathology
/ Research Article
/ Sp1 Transcription Factor - genetics
/ Sp1 Transcription Factor - metabolism
/ Surgical Orthopedics
2024
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SP1 regulates BMSC osteogenic differentiation through the miR-133a-3p/MAPK3 axis
Journal Article
SP1 regulates BMSC osteogenic differentiation through the miR-133a-3p/MAPK3 axis
2024
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Overview
Background
The progression of osteoporosis (OP) can dramatically increase the risk of fractures, which seriously disturb the life of elderly individuals. Specific protein 1 (SP1) is involved in OP progression. However, the mechanism by which SP1 regulates OP progression remains unclear.
Objective
This study investigated the mechanism underlying the function of SP1 in OP.
Methods
SAMP6 mice were used to establish an in vivo model of age-dependent OP, and BALB/c mice were used as controls. BMSCs were extracted from two subtypes of mice. Hematoxylin and eosin staining were performed to mark the intramedullary trabecular bone structure to evaluate histological changes. ChIP assay was used to assess the targeted regulation between SP1 and miR-133a-3p. The binding sites between MAPK3 and miR-133a-3p were verified using a dual-luciferase reporter assay. The mRNA levels of miR-133a-3p and MAPK3 were detected using quantitative reverse transcription polymerase chain reaction (RT-qPCR). The protein expression of SP1, MAPK3, Colla1, OCN, and Runx2 was examined using Western blotting. Alkaline phosphatase (ALP) kit and Alizarin Red S staining were used to investigate ALP activity and mineralized nodules, respectively.
Results
The levels of SP1 and miR-133a-3p were upregulated, whereas the expression of MAPK3 was downregulated in BMSCs from SAMP6 mice, and miR-133a-3p inhibitor accelerated osteogenic differentiation in BMSCs. SP1 directly targeted miR-133a-3p, and MAPK3 was the downstream mRNA of miR-133a-3p. Mechanically, SP1 accelerated osteogenic differentiation in BMSCs via transcriptional mediation of the miR-133a-3p/MAPK3 axis.
Conclusion
SP1 regulates osteogenic differentiation by mediating the miR-133a-3p/MAPK3 axis, which would shed new light on strategies for treating senile OP.
Publisher
BioMed Central
Subject
/ Cell Differentiation - genetics
/ Cell Differentiation - physiology
/ Male
/ Medicine
/ Mesenchymal Stem Cells - metabolism
/ Mice
/ Mitogen-Activated Protein Kinase 3 - genetics
/ Mitogen-Activated Protein Kinase 3 - metabolism
/ Sp1 Transcription Factor - genetics
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