Evidence map›Paper›PMID 20001822›Full record

ArticleTissue engineering. Part C, Methods2010

Bioengineered three-dimensional physiological model of colonic longitudinal smooth muscle in vitro.

Shreya Raghavan, Mai T Lam, Lesley L Foster, Robert R Gilmont, Sita Somara, Shuichi Takayama, Khalil N Bitar

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 2010. 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
0.5field-weighted citation impact, top 31% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Tissue Engineering for Gastrointestinal and Genitourinary Tracts.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Review
  8. Bioengineering the gut: future prospects of regenerative medicine.Nature reviews. Gastroenterology & hepatology · 2016
    Review
  9. Article
  10. Review
  11. Article
  12. Design strategies of biodegradable scaffolds for tissue regeneration.Biomedical engineering and computational biology · 2014
    Review
  13. Review
  14. Review
  15. Article
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 1 institution in 1 country.

Shreya RaghavanDepartment of Pediatrics-Gastroenterology, University of Michigan Medical School, Ann Arbor, Michigan 48109-0658, USA.
Mai T Lam
Lesley L Foster
Robert R Gilmont
Sita Somara
Shuichi Takayama
Khalil N Bitar
University of Michigan · US

Funding

HSP27 Association with Thin Filaments in Colonic MuscleR01DK057020 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BITAR, KHALIL N · 2001 to 2009
$2.6M
NIDDK NIH HHS R01 DK-057020
6 · The paper itself

Abstract

backgroundThe objective of this study was to develop a physiological model of longitudinal smooth muscle tissue from isolated longitudinal smooth muscle cells arranged in the longitudinal axis.

methodsLongitudinal smooth muscle cells from rabbit sigmoid colon were isolated and expanded in culture. Cells were seeded at high densities onto laminin-coated Sylgard surfaces with defined wavy microtopographies. A highly aligned cell sheet was formed, to which addition of fibrin resulted in delamination.

results(1) Acetylcholine (ACh) induced a dose-dependent, rapid, and sustained force generation. (2) Absence of extracellular calcium attenuated the magnitude and sustainability of ACh-induced force by 50% and 60%, respectively. (3) Vasoactive intestinal peptide also attenuated the magnitude and sustainability of ACh-induced force by 40% and 60%, respectively. These data were similar to force generated by longitudinal tissue. (4) Bioengineered constructs also maintained smooth muscle phenotype and calcium-dependence characteristics. SUMMARY: This is a novel physiologically relevant in vitro three-dimensional model of colonic longitudinal smooth muscle tissue. Bioengineered three-dimensional longitudinal smooth muscle presents the ability to generate force, and respond to contractile agonists and relaxant peptides similar to native longitudinal tissue. This model has potential applications to investigate the underlying pathophysiology of dysfunctional colonic motility. It also presents as a readily implantable band-aid colonic longitudinal muscle tissue.

Indexed as

Tissue EngineeringAnimalsCalciumCells, CulturedColonCulture MediaFluorescent Antibody TechniqueMuscle, SmoothRabbitsCalciumCulture Media

Identifiers

PMID20001822
PMCPMC2943406
OpenAlexW2171834683

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.