Evidence map›Paper›PMID 28592272›Full record

ArticleJournal of translational medicine2017

Betaine promotes cell differentiation of human osteoblasts in primary culture.

Isabella Villa, Pamela Senesi, Anna Montesano, Anita Ferraretto, Fernanda Vacante, Alice Spinello, Michela Bottani, Simona Bolamperti, Alessandro Rubinacci, Livio Luzi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Isabella VillaBone Metabolism Unit, San Raffaele Scientific Institute, Milan, Italy.
Pamela SenesiMetabolism Research Center, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.
Anna MontesanoDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Anita FerrarettoMetabolism Research Center, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.
Fernanda VacanteMetabolism Research Center, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.
Alice SpinelloBone Metabolism Unit, San Raffaele Scientific Institute, Milan, Italy.
Michela BottaniDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Simona BolampertiBone Metabolism Unit, San Raffaele Scientific Institute, Milan, Italy.
Alessandro RubinacciBone Metabolism Unit, San Raffaele Scientific Institute, Milan, Italy.
Livio LuziMetabolism Research Center, IRCCS Policlinico San Donato, San Donato Milanese, Milan, Italy.
Ileana TerruzziDiabetes Research Institute, Metabolism, Nutrigenomics and Cellular Differentiation Unit, San Raffaele Scientific Institute, 60 Olgettina street, 20132, Milan, Italy. terruzzi.ileana@hsr.it.
University of Milan · ITIRCCS Policlinico San Donato · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBetaine (BET), a component of many foods, is an essential osmolyte and a source of methyl groups; it also shows an antioxidant activity. Moreover, BET stimulates muscle differentiation via insulin like growth factor I (IGF-I). The processes of myogenesis and osteogenesis involve common mechanisms with skeletal muscle cells and osteoblasts sharing the same precursor. Therefore, we have hypothesized that BET might be effective on osteoblast cell differentiation.

methodsThe effect of BET was tested in human osteoblasts (hObs) derived from trabecular bone samples obtained from waste material of orthopedic surgery. Cells were treated with 10 mM BET at 5, 15, 60 min and 3, 6 and 24 h. The possible effects of BET on hObs differentiation were evaluated by real time PCR, western blot and immunofluorescence analysis. Calcium imaging was used to monitor intracellular calcium changes.

resultsReal time PCR results showed that BET stimulated significantly the expression of RUNX2, osterix, bone sialoprotein and osteopontin. Western blot and immunofluorescence confirmed BET stimulation of osteopontin protein synthesis. BET stimulated ERK signaling, key pathway involved in osteoblastogenesis and calcium signaling. BET induced a rise of intracellular calcium by means of the calcium ions influx from the extracellular milieu through the L-type calcium channels and CaMKII signaling activation. A significant rise in IGF-I mRNA at 3 and 6 h and a significant increase of IGF-I protein at 6 and 24 h after BET stimulus was detected. Furthermore, BET was able to increase significantly both SOD2 gene expression and protein content.

conclusionsOur study showed that three signaling pathways, i.e. cytosolic calcium influx, ERK activation and IGF-I production, are enhanced by BET in human osteoblasts. These pathways could have synergistic effects on osteogenic gene expression and protein synthesis, thus potentially leading to enhanced bone formation. Taken together, these results suggest that BET could be a promising nutraceutical therapeutic agent in the strategy to counteract the concomitant and interacting impact of sarcopenia and osteoporosis, i.e. the major determinants of senile frailty and related mortality.

Indexed as

AgedAged, 80 and overBetaineCalciumCell DifferentiationCells, CulturedGene Expression RegulationHumansMembrane PotentialsModels, BiologicalOsteoblastsOsteogenesisSignal TransductionSuperoxide DismutaseBetaineCalciumSuperoxide DismutaseAgingBoneCalcium signalingIGF-INutraceutical

Identifiers

PMID28592272
PMCPMC5463390
OpenAlexW2623454131

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.