Evidence map›Paper›PMID 31183683›Full record

ArticleIn vitro cellular & developmental biology. Animal2019

Development and characterization of a stable bovine intestinal sub-epithelial myofibroblast cell line from ileum of a young calf.

Tirth Uprety, Brionna B Spurlin, Linto Antony, Chithra Sreenivasan, Alan Young, Feng Li, Michael B Hildreth, Radhey S Kaushik

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Tirth UpretyDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Brionna B SpurlinDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Linto AntonyDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, 57007, USA.
Chithra SreenivasanDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Alan YoungDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, 57007, USA.
Feng LiDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Michael B HildrethDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Radhey S KaushikDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA. radhey.kaushik@sdstate.edu.ORCID http://orcid.org/0000-0003-4204-9323
South Dakota State University · US

Funding

Cooperative State Research, Education, and Extension Service 2004-35605-14243National Institute of Food and Agriculture SD00H547-15
6 · The paper itself

Abstract

Intestinal sub-epithelial myofibroblasts (ISEMFs) are mesenchymal cells that do not express cytokeratin but express α-smooth muscle actin and vimentin. Despite being cells with diverse functions, there is a paucity of knowledge about their origin and functions primarily due to the absence of a stable cell line. Although myofibroblast in vitro models for human, mouse, and pig are available, there is no ISEMF cell line available from young calves. We isolated and developed an ileal ISEMF cell line from a 2-d-old calf that expressed α-smooth muscle actin and vimentin but no cytokeratin indicating true myofibroblast cells. To overcome replicative senescence, we immortalized primary cells with SV40 large T antigen. We characterized and compared both primary and immortalized ileal ISEMF cells for surface glycan and Toll-like-receptor (TLR) expression by lectin-binding assay and real-time quantitative PCR (RT-qPCR) assay respectively. SV40 immortalization significantly decreased surface lectin binding for lectins GSL-I, PHA-L, ECL, Jacalin, Con-A, LCA, and LEL. Both cell types expressed TLRs 1-9 and showed no significant differences in TLR expression. Thus, these cells can be useful in vitro model to study ISEMF's origin, physiology, and functions.

Indexed as

ActinsAnimalsAntigens, Polyomavirus TransformingAntigens, Viral, TumorCattleCell Culture TechniquesCell Line, TransformedIleumIntestinal MucosaKeratinsMyofibroblastsToll-Like ReceptorsVimentinActinsAntigens, Polyomavirus TransformingAntigens, Viral, TumorKeratinsToll-Like ReceptorsVimentinBovineIntestinal sub-epithelial myofibroblastLectinToll-like receptors

Identifiers

PMID31183683
OpenAlexW2949390515

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.