Evidence map›Paper›PMID 27494521›Full record

ArticlePloS one2016

Characterization of Cells Isolated from Genetic and Trauma-Induced Heterotopic Ossification.

Shailesh Agarwal, James Drake, Ammar T Qureshi, Shawn Loder, Shuli Li, Kay Shigemori, Jonathan Peterson, David Cholok, Jonathan A Forsberg, Yuji Mishina and 2 more

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Methods for the reliable induction of heterotopic ossification in the conditionalJournal of musculoskeletal & neuronal interactions · 2020
    Article
  8. Elevated BMP and Mechanical Signaling Through YAP1/RhoA Poises FOP Mesenchymal Progenitors for Osteogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  9. Review
  10. Review
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

12 authors.

Shailesh AgarwalDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
James DrakeDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
Ammar T QureshiDepartment of Regenerative Medicine, Naval Medical Research Center, Silver Spring, MD, 20910, United States of America.
Shawn LoderDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
Shuli LiDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
Kay ShigemoriDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
Jonathan PetersonDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
David CholokDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
Jonathan A ForsbergDepartment of Regenerative Medicine, Naval Medical Research Center, Silver Spring, MD, 20910, United States of America.
Yuji MishinaDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.
Thomas A DavisDepartment of Regenerative Medicine, Naval Medical Research Center, Silver Spring, MD, 20910, United States of America.
Benjamin LeviDepartment of Surgery, University of Michigan Health Systems, Ann Arbor, MI, 48109, United States of America.

Funding

Molecular pathogenesis of craniosynostosis caused by enhanced BMP signalingR01DE020843 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MISHINA, YUJI · 2010 to 2019
$4.9M
Novel Pathway and Prevention Strategy for Heterotopic OssificationK08GM109105 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEVI, BENJAMIN · 2014 to 2017
$785k
Targeting Inflammation and BMP Signaling in Osteoprogenitor Cells of Heterotopic OssificationF32AR066499 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AGARWAL, SHAILESH · 2015 to 2015
$54k
NIAMS NIH HHS F32 AR066499NIDCR NIH HHS R01 DE020843NIGMS NIH HHS K08 GM109105
6 · The paper itself

Abstract

Heterotopic ossification (HO) is the pathologic formation of bone separate from the normal skeleton. Although several models exist for studying HO, an understanding of the common in vitro properties of cells isolated from these models is lacking. We studied three separate animal models of HO including two models of trauma-induced HO and one model of genetic HO, and human HO specimens, to characterize the properties of cells derived from tissue containing pre-and mature ectopic bone in relation to analogous mesenchymal cell populations or osteoblasts obtained from normal muscle tissue. We found that when cultured in vitro, cells isolated from the trauma sites in two distinct models exhibited increased osteogenic differentiation when compared to cells isolated from uninjured controls. Furthermore, osteoblasts isolated from heterotopic bone in a genetic model of HO also exhibited increased osteogenic differentiation when compared with normal osteoblasts. Finally, osteoblasts derived from mature heterotopic bone obtained from human patients exhibited increased osteogenic differentiation when compared with normal bone from the same patients. These findings demonstrate that across models, cells derived from tissues forming heterotopic ossification exhibit increased osteogenic differentiation when compared with either normal tissues or osteoblasts. These cell types can be used in the future for in vitro investigations for drug screening purposes.

Indexed as

AdultAnimalsBone and BonesBurnsCell DifferentiationCell ProliferationCells, CulturedCore Binding Factor Alpha 1 SubunitDisease Models, AnimalHumansMaleMesenchymal Stem CellsMiceMice, Inbred C57BLMice, TransgenicMusclesCore Binding Factor Alpha 1 SubunitOsteocalcinSmad1 ProteinSmad5 ProteinSp7 protein, mouseSp7 Transcription FactorTranscription Factors

Identifiers

PMID27494521
PMCPMC4975503

What OpenQuestion holds

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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.