Evidence map›Paper›PMID 29214530›Full record

ReviewAnalytical and bioanalytical chemistry2018

Microfluidic systems for studying dynamic function of adipocytes and adipose tissue.

Xiangpeng Li, Christopher J Easley

Abstract readReview
In one paragraph

Review in Analytical and bioanalytical chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Novel Role of the SIRT1 in Endocrine and Metabolic Diseases.International journal of biological sciences · 2023
    Review
  4. Signaling pathways in obesity: mechanisms and therapeutic interventions.Signal transduction and targeted therapy · 2022
    Review
  5. Article
  6. Autologous Human Immunocompetent White Adipose Tissue-on-Chip.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  7. Review
  8. Towards an Insulin Resistant Adipose Model on a Chip.Cellular and molecular bioengineering · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Microfluidics for interrogating live intact tissues.Microsystems & nanoengineering · 2020
    Review
  14. 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

2 authors.

Xiangpeng LiDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL, 36849, USA.
Christopher J EasleyDepartment of Chemistry and Biochemistry, Auburn University, Auburn, AL, 36849, USA. chris.easley@auburn.edu.

Funding

Unmasking mechanisms of lipolytic dynamics in adipose tissue using high-resolution microfluidic samplingR01DK093810 · NIDDK · AUBURN UNIVERSITY AT AUBURN · PI EASLEY, CHRISTOPHER J · 2012 to 2023
$3.8M
National Institute of Diabetes and Digestive and Kidney Diseases DK093810NIDDK NIH HHS R01 DK093810
6 · The paper itself

Abstract

Recent breakthroughs in organ-on-a-chip and related technologies have highlighted the extraordinary potential for microfluidics to not only make lasting impacts in the understanding of biological systems but also to create new and important in vitro culture platforms. Adipose tissue (fat), in particular, is one that should be amenable to microfluidic mimics of its microenvironment. While the tissue was traditionally considered important only for energy storage, it is now understood to be an integral part of the endocrine system that secretes hormones and responds to various stimuli. As such, adipocyte function is central to the understanding of pathological conditions such as obesity, diabetes, and metabolic syndrome. Despite the importance of the tissue, only recently have significant strides been made in studying dynamic function of adipocytes or adipose tissues on microfluidic devices. In this critical review, we highlight new developments in the special class of microfluidic systems aimed at culture and interrogation of adipose tissue, a sub-field of microfluidics that we contend is only in its infancy. We close by reflecting on these studies as we forecast a promising future, where microfluidic technologies should be capable of mimicking the adipose tissue microenvironment and provide novel insights into its physiological roles in the normal and diseased states. Graphical abstract This critical review focuses on recent developments and challenges in applying microfluidic systems to the culture and analysis of adipocytes and adipose tissue.

Indexed as

AdipocytesAdipokinesAdipose TissueAnimalsCell Culture TechniquesEquipment DesignFatty AcidsGlucoseHormonesHumansInsulinMicrofluidic Analytical TechniquesTissue Culture TechniquesAdipokinesFatty AcidsGlucoseHormonesInsulinAdipocyteAdipokineBatokineBioanalytical methodsHormoneMicrofluidics microfabrication

Identifiers

PMID29214530
PMCPMC5789454

What OpenQuestion holds

Textmetadata
LicenceTDM
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.