MicroRNA-100 inhibits bone morphogenetic protein-induced osteoblast differentiation by targeting Smad1
OBJECTIVE: MicroRNAs (miRNAs) act as key regulators of diverse cellular activities by regulating the expression of protein-coding genes. Osteoblast differentiation, a fundamental step in skeletal development, involves the activation of several signaling pathways, including transforming growth factor β (TGF-β), bone morphogenetic protein (BMP), and Wnt signaling pathways.
MATERIALS AND METHODS: miRNA expression was measured using TaqManRT-PCR. Western blot was used to detect the protein expression of Smad1. Luciferase reporter assay was used to measure the luciferase activity.
RESULTS: In this study, we found that miR-100 was expressed in mesenchymal progenitor cell lines; furthermore, its expression was reduced during osteoblast differentiation. Retroviral overexpression of miR-100 decreased Smad1 protein levels, whereas miR-100 inhibition had the opposite effect, suggesting that miR-100 acts as an endogenous attenuator of Smad1 in osteoblast differentiation.
CONCLUSIONS: Together, our data demonstrate that miR-100 acts as an important endogenous negative regulator of BMP-induced osteoblast differentiation.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2016 |
---|---|
Erschienen: |
2016 |
Enthalten in: |
Zur Gesamtaufnahme - volume:20 |
---|---|
Enthalten in: |
European review for medical and pharmacological sciences - 20(2016), 18 vom: 01. Sept., Seite 3911-3919 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Fu, H-L [VerfasserIn] |
---|
Themen: |
Bone Morphogenetic Proteins |
---|
Anmerkungen: |
Date Completed 07.08.2017 Date Revised 18.03.2018 published: Print Citation Status MEDLINE |
---|
Förderinstitution / Projekttitel: |
|
---|
PPN (Katalog-ID): |
NLM265259061 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM265259061 | ||
003 | DE-627 | ||
005 | 20231224211905.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2016 xx |||||o 00| ||eng c | ||
028 | 5 | 2 | |a pubmed24n0884.xml |
035 | |a (DE-627)NLM265259061 | ||
035 | |a (NLM)27735023 | ||
035 | |a (PII)11467 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Fu, H-L |e verfasserin |4 aut | |
245 | 1 | 0 | |a MicroRNA-100 inhibits bone morphogenetic protein-induced osteoblast differentiation by targeting Smad1 |
264 | 1 | |c 2016 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 07.08.2017 | ||
500 | |a Date Revised 18.03.2018 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a OBJECTIVE: MicroRNAs (miRNAs) act as key regulators of diverse cellular activities by regulating the expression of protein-coding genes. Osteoblast differentiation, a fundamental step in skeletal development, involves the activation of several signaling pathways, including transforming growth factor β (TGF-β), bone morphogenetic protein (BMP), and Wnt signaling pathways | ||
520 | |a MATERIALS AND METHODS: miRNA expression was measured using TaqManRT-PCR. Western blot was used to detect the protein expression of Smad1. Luciferase reporter assay was used to measure the luciferase activity | ||
520 | |a RESULTS: In this study, we found that miR-100 was expressed in mesenchymal progenitor cell lines; furthermore, its expression was reduced during osteoblast differentiation. Retroviral overexpression of miR-100 decreased Smad1 protein levels, whereas miR-100 inhibition had the opposite effect, suggesting that miR-100 acts as an endogenous attenuator of Smad1 in osteoblast differentiation | ||
520 | |a CONCLUSIONS: Together, our data demonstrate that miR-100 acts as an important endogenous negative regulator of BMP-induced osteoblast differentiation | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Bone Morphogenetic Proteins |2 NLM | |
650 | 7 | |a MIRN100 microRNA, human |2 NLM | |
650 | 7 | |a MicroRNAs |2 NLM | |
700 | 1 | |a Pan, H-X |e verfasserin |4 aut | |
700 | 1 | |a Zhao, B |e verfasserin |4 aut | |
700 | 1 | |a Dong, B-C |e verfasserin |4 aut | |
700 | 1 | |a Shao, L |e verfasserin |4 aut | |
700 | 1 | |a Fu, G-S |e verfasserin |4 aut | |
700 | 1 | |a Wang, Q |e verfasserin |4 aut | |
700 | 1 | |a Li, M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t European review for medical and pharmacological sciences |d 1997 |g 20(2016), 18 vom: 01. Sept., Seite 3911-3919 |w (DE-627)NLM09387944X |x 2284-0729 |7 nnns |
773 | 1 | 8 | |g volume:20 |g year:2016 |g number:18 |g day:01 |g month:09 |g pages:3911-3919 |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 20 |j 2016 |e 18 |b 01 |c 09 |h 3911-3919 |