Evidence map›Paper›PMID 30284537›Full record

ArticleBiofabrication2018

Engineering of microscale vascularized fat that responds to perfusion with lipoactive hormones.

Xuanyue Li, Jingyi Xia, Calin T Nicolescu, Miles W Massidda, Tyler J Ryan, Joe Tien

Abstract readEvaluation Study
In one paragraph

Article in Biofabrication, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Biofabrication of engineered blood vessels for biomedical applications.Science and technology of advanced materials · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Microfluidic Biomaterials.Advanced healthcare materials · 2021
    Review
  14. Article
  15. Tissue Engineering of the Microvasculature.Comprehensive Physiology · 2019
    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

6 authors.

Xuanyue LiDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, United States of America.
Jingyi XiaDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, United States of America.
Calin T NicolescuDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, United States of America.
Miles W MassiddaDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, United States of America.
Tyler J RyanDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, United States of America.ORCID 0000-0003-2506-8901
Joe TienDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, United States of America.ORCID 0000-0003-4283-3986

Funding

Translational Research in BiomaterialsT32EB006359 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MARK W. GRINSTAFF, Michelle H Teplensky · 2009 to 2026
$4.2M
Engineered Invasive Human Breast Tumors with Integrated Capillaries and LymphaticsU01CA214292 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NELSON, CELESTE M, TIEN, JOE Y · 2017 to 2021
$3.2M
In Vivo Microsurgical Anastomosis of Prevascularized TissuesR03EB018851 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI TIEN, JOE Y · 2014 to 2015
$164k
NCI NIH HHS U01 CA214292NIBIB NIH HHS R03 EB018851NIBIB NIH HHS T32 EB006359
6 · The paper itself

Abstract

Current methods to treat large soft-tissue defects mainly rely on autologous transfer of adipocutaneous flaps, a method that is often limited by donor site availability. Engineered vascularized adipose tissues can potentially be a viable and readily accessible substitute to autologous flaps. In this study, we engineered a small-scale adipose tissue with pre-patterned vasculature that enables immediate perfusion. Vessels formed after one day of perfusion and displayed barrier function after three days of perfusion. Under constant perfusion, adipose tissues remained viable and responded to lipoactive hormones insulin and epinephrine with lipid accumulation and loss, respectively. Adipocyte growth correlated inversely with distance away from the feeding vessel, as predicted by a Krogh-type model.

Indexed as

AdipocytesAdipose TissueAnimalsCell ProliferationEpinephrineHormonesHumansInsulinLipid MetabolismMiceMicrovesselsNIH 3T3 CellsPerfusionTissue EngineeringEpinephrineHormonesInsulin

Identifiers

PMID30284537
PMCPMC6252090

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.