Evidence map›Paper›PMID 39359127›Full record

ArticleBiomaterials science2024

LAPONITE® nano-silicates potentiate the angiogenic effects of FG-4592 and osteogenic effects of BMP-2.

Bipin Gaihre, Emily Camilleri, Maryam Tilton, Maria D Astudillo Potes, Xifeng Liu, Fabrice Lucien, Lichun Lu

Abstract read
In one paragraph

Article in Biomaterials science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Bipin GaihreDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA. Lu.Lichun@mayo.edu.ORCID http://orcid.org/0009-0000-2596-7427
Emily CamilleriDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA. Lu.Lichun@mayo.edu.
Maryam TiltonDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA. Lu.Lichun@mayo.edu.
Maria D Astudillo PotesDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA. Lu.Lichun@mayo.edu.
Xifeng LiuDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA. Lu.Lichun@mayo.edu.ORCID http://orcid.org/0000-0002-2684-6309
Fabrice LucienDepartment of Urology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID http://orcid.org/0000-0001-6149-345X
Lichun LuDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA. Lu.Lichun@mayo.edu.

Funding

Metastatic Spine Tumors: Minimally Invasive Fracture Risk Analysis and Treatment - MasterR01AR056212 · NIAMS · MAYO CLINIC ROCHESTER · PI Benjamin D Elder, Lichun Lu · 2008 to 2026
$6.2M
Injectable and Moldable Composite Bone Scaffolds for Spinal FusionR01AR075037 · NIAMS · MAYO CLINIC ROCHESTER · PI ELDER, BENJAMIN D, LU, LICHUN · 2019 to 2023
$2.5M
NIAMS NIH HHS R01 AR056212NIAMS NIH HHS R01 AR075037
6 · The paper itself

Abstract

LAPONITE®-based drug delivery systems offer many advantages due to the unique ionic and physical properties of LAPONITE®. The high ionicity and large surface area of LAPONITE® nanoparticles enable the intercalation and dissolution of biomolecules. In this study, we explored the potential of LAPONITE® as a carrier for FG-4592 to support angiogenesis and as a carrier for bone morphogenic protein-2 (BMP-2) to support osteogenesis. Interestingly, we found that LAPONITE® promoted the FG-4592 induced upregulation of vascular endothelial growth factor (VEGF) gene expression of human umbilical cord endothelial cells (HUVECs). Additionally, we observed that LAPONITE® could provide a sustained release of BMP-2 and significantly potentiate the osteogenic effects of BMP-2 on adipose derived mesenchymal stem cells (AMSCs). Overall, current findings on the LAPONITE®-drug/protein model system provide a unique way to potentiate the angiogenic activities of FG-4592 on HUVECs and osteogenic effects of BMP-2 on AMSCs for tissue engineering application. Future studies will be directed towards gaining a deeper understanding of these effects on a co-culture system of HUVECs and AMSCs.

Indexed as

Bone Morphogenetic Protein 2Mesenchymal Stem CellsNeovascularization, PhysiologicOsteogenesisSilicatesCell DifferentiationCells, CulturedHumansHuman Umbilical Vein Endothelial CellsNanoparticlesVascular Endothelial Growth Factor ABMP2 protein, humanBone Morphogenetic Protein 2laponiteSilicatesVascular Endothelial Growth Factor A

Identifiers

PMID39359127
PMCPMC11822916

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Registered trials

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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.