Evidence map›Paper›PMID 28841424›Full record

ArticleStem cell research2017

Mechanical induction of dentin-like differentiation by adult mouse bone marrow stromal cells using compressive scaffolds.

Basma Hashmi, Tadanori Mammoto, James Weaver, Thomas Ferrante, Amanda Jiang, Elisabeth Jiang, Juani Feliz, Donald E Ingber

Abstract read
In one paragraph

Article in Stem cell research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Mechanical control in dental and jaw morphogenesis and remodeling.International journal of oral science · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. From mechanobiology to developmentally inspired engineering.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  9. 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

8 authors.

Basma HashmiVascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Tadanori MammotoVascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.
James WeaverWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
Thomas FerranteWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
Amanda JiangVascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Elisabeth JiangVascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Juani FelizWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
Donald E IngberVascular Biology Program and Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA; Harvard John A. Paulson School of Engineering and Applied Sciences, Cambridge, MA 02138, USA. Electronic address: don.ingber@wyss.harvard.edu.

Funding

Micromechanical Determinants of Organ Design and Engineering (SysCODE 6 of 10)RL1DE019023 · NIDCR · BOSTON CHILDREN'S HOSPITAL · PI INGBER, DONALD E · 2007 to 2011
$2.9M
NIDCR NIH HHS RL1 DE019023
6 · The paper itself

Abstract

Tooth formation during embryogenesis is controlled through a complex interplay between mechanical and chemical cues. We have previously shown that physical cell compaction of dental mesenchyme cells during mesenchymal condensation is responsible for triggering odontogenic differentiation during embryogenesis, and that expression of Collagen VI stabilizes this induction. In addition, we have shown that synthetic polymer scaffolds that artificially induce cell compaction can induce embryonic mandible mesenchymal cells to initiate tooth differentiation both in vitro and in vivo. As embryonic cells would be difficult to use for regenerative medicine applications, here we explored whether compressive scaffolds coated with Collagen VI can be used to induce adult bone marrow stromal cells (BMSCs) to undergo an odontogenic lineage switch. These studies revealed that when mouse BMSCs are compressed using these scaffolds they increase expression of critical markers of tooth differentiation in vitro, including the key transcription factors Pax9 and Msx1. Implantation under the kidney capsule of contracting scaffolds bearing these cells in mice also resulted in local mineralization, calcification and production of dentin-like tissue. These findings show that these chemically-primed compressive scaffolds can be used to induce adult BMSCs to undergo a lineage switch and begin to form dentin-like tissue, thus raising the possibility of using adult BMSCs for future tooth regeneration applications.

Indexed as

Cell DifferentiationStress, MechanicalAgingAnimalsDentinMesenchymal Stem CellsMiceMicroscopy, FluorescenceRNA, MessengerTissue ScaffoldsTranscription FactorsRNA, MessengerTranscription FactorsBone marrow stromal cellsCollagen VIDentinOdontogenesisPNIPAAmTissue engineering

Identifiers

PMID28841424
PMCPMC5796538

What OpenQuestion holds

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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.