Evidence map›Paper›PMID 39041616›Full record

ReviewTissue engineering. Part B, Reviews2025

An Exploration of the Role of Osteoclast Lineage Cells in Bone Tissue Engineering.

Eoin J Devoy, Erfan Jabari, George Kotsanos, Robert H Choe, John P Fisher

Abstract readReview
In one paragraph

Review in Tissue engineering. Part B, Reviews, 2025. 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

5 authors.

Eoin J DevoyFischell Department of Bioengineering, University of Maryland, College Park, Maryland, USA.
Erfan JabariFischell Department of Bioengineering, University of Maryland, College Park, Maryland, USA.
George KotsanosFischell Department of Bioengineering, University of Maryland, College Park, Maryland, USA.
Robert H ChoeFischell Department of Bioengineering, University of Maryland, College Park, Maryland, USA.ORCID 0000-0002-4834-4529
John P FisherFischell Department of Bioengineering, University of Maryland, College Park, Maryland, USA.

Funding

Training and Dissemination CoreP41EB023833 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI FISHER, JOHN P, MIKOS, ANTONIOS G. · 2017 to 2021
$6.2M
3D Bioprinted Nipple-Areolar Complex ImplantsR01HD112031 · NICHD · UNIV OF MARYLAND, COLLEGE PARK · PI John P Fisher · 2023 to 2026
$2.2M
Multiscale hydrogel biomaterials-enabled 3D modeling of cancer drug resistanceR01CA279815 · NCI · UNIV OF MARYLAND, COLLEGE PARK · PI Wenquan Ou · 2023 to 2026
$1.7M
NCI NIH HHS R01 CA279815NIBIB NIH HHS P41 EB023833NICHD NIH HHS R01 HD112031
6 · The paper itself

Abstract

Bone defects because of age, trauma, and surgery, which are exacerbated by medication side effects and common diseases such as osteoporosis, diabetes, and rheumatoid arthritis, are a problem of epidemic scale. The present clinical standard for treating these defects includes autografts and allografts. Although both treatments can promote robust regenerative outcomes, they fail to strike a desirable balance of availability, side effect profile, consistent regenerative efficacy, and affordability. This difficulty has contributed to the rise of bone tissue engineering (BTE) as a potential avenue through which enhanced bone regeneration could be delivered. BTE is founded upon a paradigm of using biomaterials, bioactive factors, osteoblast lineage cells (ObLCs), and vascularization to cue deficient bone tissue into a state of regeneration. Despite promising preclinical results, BTE has had modest success in being translated into the clinical setting. One barrier has been the simplicity of its paradigm relative to the complexity of biological bone. Therefore, this paradigm must be critically examined and expanded to better account for this complexity. One potential avenue for this is a more detailed consideration of osteoclast lineage cells (OcLCs). Although these cells ostensibly oppose ObLCs and bone regeneration through their resorptive functions, a myriad of investigations have shed light on their potential to influence bone equilibrium in more complex ways through their interactions with both ObLCs and bone matrix. Most BTE research has not systematically evaluated their influence. Yet contrary to expectations associated with the paradigm, a selection of BTE investigations has demonstrated that this influence can enhance bone regeneration in certain contexts. In addition, much work has elucidated the role of many controllable scaffold parameters in both inhibiting and stimulating the activity of OcLCs in parallel to bone regeneration. Therefore, this review aims to detail and explore the implications of OcLCs in BTE and how they can be leveraged to improve upon the existing BTE paradigm.

Indexed as

Bone and BonesBone RegenerationCell LineageOsteoclastsTissue EngineeringAnimalsHumansbone tissue engineeringco-culturehydrogelosteoblastosteoclast

Identifiers

PMID39041616
PMCPMC13625628

What OpenQuestion holds

Textmetadata
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.