Evidence map›Paper›PMID 28670447›Full record

ArticleRSC advances2017

Short-term hypoxic preconditioning promotes prevascularization in 3D bioprinted bone constructs with stromal vascular fraction derived cells.

Mitchell A Kuss, Robert Harms, Shaohua Wu, Ying Wang, Jason B Untrauer, Mark A Carlson, Bin Duan

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
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

34 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  10. Up-to-date progress in bioprinting of bone tissue.International journal of bioprinting · 2023
    Review
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  13. Article
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  16. State of the field: cellular and exosomal therapeutic approaches in vascular regeneration.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  17. Article
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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 at 3 institutions in 2 countries.

Mitchell A KussMary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE, USA. Email: bin.duan@unmc.edu; Tel: +1 402 559 9637.
Robert HarmsMary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE, USA. Email: bin.duan@unmc.edu; Tel: +1 402 559 9637.
Shaohua WuMary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE, USA. Email: bin.duan@unmc.edu; Tel: +1 402 559 9637.
Ying WangMary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE, USA. Email: bin.duan@unmc.edu; Tel: +1 402 559 9637.
Jason B UntrauerDivision of Oral & Maxillofacial Surgery, Department of Surgery, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Mark A CarlsonMary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE, USA. Email: bin.duan@unmc.edu; Tel: +1 402 559 9637.ORCID 0000-0002-8113-9199
Bin DuanMary & Dick Holland Regenerative Medicine Program, University of Nebraska Medical Center, Omaha, NE, USA. Email: bin.duan@unmc.edu; Tel: +1 402 559 9637.ORCID 0000-0002-5647-3793
University of Nebraska Medical Center · USNational Medical Research Center of Dentistry and Maxillofacial Surgery · RUVA Nebraska Western Iowa Health Care System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reconstruction of complex, craniofacial bone defects often requires autogenous vascularized bone grafts, and still remains a challenge today. In order to address this issue, we isolated the stromal vascular fraction (SVF) from adipose tissues and maintained the phenotypes and the growth of endothelial lineage cells within SVF derived cells (SVFC) by incorporating an endothelial cell medium. We 3D bioprinted SVFC within our hydrogel bioinks and conditioned the constructs in either normoxia or hypoxia. We found that short-term hypoxic conditioning promoted vascularization-related gene expression, whereas long-term hypoxia impaired cell viability and vascularization. 3D bioprinted bone constructs composed of polycaprolactone/hydroxyapatite (PCL/HAp) and SVFC-laden hydrogel bioinks were then implanted into athymic mice, after conditioning in normoxic or short-term hypoxic environments, in order to determine the

Identifiers

PMID28670447
PMCPMC5472052
OpenAlexW2622683133

What OpenQuestion holds

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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.