Evidence map›Paper›PMID 28456657›Full record

ArticleActa biomaterialia2017

Topography of calcium phosphate ceramics regulates primary cilia length and TGF receptor recruitment associated with osteogenesis.

Jingwei Zhang, Melis T Dalbay, Xiaoman Luo, Erik Vrij, Davide Barbieri, Lorenzo Moroni, Joost D de Bruijn, Clemens A van Blitterswijk, J Paul Chapple, Martin M Knight and 1 more

Abstract read
In one paragraph

Article in Acta biomaterialia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Calcium Phosphate-Based Biomaterials for Bone Repair.Journal of functional biomaterials · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
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.

Jingwei ZhangComplex Tissue Regeneration Department, MERLN Institute for Technology Inspired Regenerative Medicine, Maastricht University, Universiteitsingel 40, 6229 ER, The Netherlands; Institute for Translational Medicine, Zhejiang University, Hangzhou, Zhejiang Province 310029, China.
Melis T DalbayInstitute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, Mile End Rd, London E1 4NS, UK.
Xiaoman LuoXpand Biotechnology BV, Bilthoven, The Netherlands.
Erik VrijComplex Tissue Regeneration Department, MERLN Institute for Technology Inspired Regenerative Medicine, Maastricht University, Universiteitsingel 40, 6229 ER, The Netherlands.
Davide BarbieriXpand Biotechnology BV, Bilthoven, The Netherlands.
Lorenzo MoroniComplex Tissue Regeneration Department, MERLN Institute for Technology Inspired Regenerative Medicine, Maastricht University, Universiteitsingel 40, 6229 ER, The Netherlands.
Joost D de BruijnInstitute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, Mile End Rd, London E1 4NS, UK; Xpand Biotechnology BV, Bilthoven, The Netherlands; Department of Biomaterials Science and Technology, MIRA Institute for Biomedical Technology and Technical Medicine, University of Twente, P.O. Box 217, 7500AE Enschede, The Netherlands.
Clemens A van BlitterswijkComplex Tissue Regeneration Department, MERLN Institute for Technology Inspired Regenerative Medicine, Maastricht University, Universiteitsingel 40, 6229 ER, The Netherlands.
J Paul ChappleWilliam Harvey Research Institute, Queen Mary University of London, Charterhouse Square, London E1 4NS, UK.
Martin M KnightInstitute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, Mile End Rd, London E1 4NS, UK. Electronic address: m.m.knight@qmul.ac.uk.
Huipin YuanComplex Tissue Regeneration Department, MERLN Institute for Technology Inspired Regenerative Medicine, Maastricht University, Universiteitsingel 40, 6229 ER, The Netherlands; Xpand Biotechnology BV, Bilthoven, The Netherlands; National Engineering Research Center for Biomaterials, Sichuan University, 610064 Chengdu, China. Electronic address: h.yuan@maastrichtuniversity.nl.

Funding

Medical Research Council MR/L002876/1
6 · The paper itself

Abstract

The surface topography of synthetic biomaterials is known to play a role in material-driven osteogenesis. Recent studies show that TGFβ signalling also initiates osteogenic differentiation. TGFβ signalling requires the recruitment of TGFβ receptors (TGFβR) to the primary cilia. In this study, we hypothesize that the surface topography of calcium phosphate ceramics regulates stem cell morphology, primary cilia structure and TGFβR recruitment to the cilium associated with osteogenic differentiation. We developed a 2D system using two types of tricalcium phosphate (TCP) ceramic discs with identical chemistry. One sample had a surface topography at micron-scale (TCP-B, with a bigger surface structure dimension) whilst the other had a surface topography at submicron scale (TCP-S, with a smaller surface structure dimension). In the absence of osteogenic differentiation factors, human bone marrow stromal cells (hBMSCs) were more spread on TCP-S than on TCP-B with alterations in actin organization and increased primary cilia prevalence and length. The cilia elongation on TCP-S was similar to that observed on glass in the presence of osteogenic media and was followed by recruitment of transforming growth factor-β RII (p-TGFβ RII) to the cilia axoneme. This was associated with enhanced osteogenic differentiation of hBMSCs on TCP-S, as shown by alkaline phosphatase activity and gene expression for key osteogenic markers in the absence of additional osteogenic growth factors. Similarly, in vivo after a 12-week intramuscular implantation in dogs, TCP-S induced bone formation while TCP-B did not. It is most likely that the surface topography of calcium phosphate ceramics regulates primary cilia length and ciliary recruitment of p-TGFβ RII associated with osteogenesis and bone formation. This bioengineering control of osteogenesis via primary cilia modulation may represent a new type of biomaterial-based ciliotherapy for orthopedic, dental and maxillofacial surgery applications. STATEMENT OF SIGNIFICANCE: The surface topography of synthetic biomaterials plays important roles in material-driven osteogenesis. The data presented herein have shown that the surface topography of calcium phosphate ceramics regulates mesenchymal stromal cells (e.g., human bone marrow mesenchymal stromal cells, hBMSCs) with respect to morphology, primary cilia structure and TGFβR recruitment to the cilium associated with osteogenic differentiation in vitro. Together with bone formation in vivo, our results suggested a new type of biomaterial-based ciliotherapy for orthopedic, dental and maxillofacial surgery by the bioengineering control of osteogenesis via primary cilia modulation.

Indexed as

Calcium PhosphatesCeramicsAnimalsBone Marrow CellsCiliaDogsHumansOsteogenesisReceptors, Transforming Growth Factor betaStromal Cellsbeta-tricalcium phosphateCalcium PhosphatesReceptors, Transforming Growth Factor betaBoneCalcium phosphate ceramicMesenchymal stromal cellPrimary ciliaTGFβTopography

Identifiers

PMID28456657
PMCPMC5489417

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.