Evidence map›Paper›PMID 35163236›Full record

ArticleInternational journal of molecular sciences2022

Toward Xeno-Free Differentiation of Human Induced Pluripotent Stem Cell-Derived Small Intestinal Epithelial Cells.

Jaakko Saari, Fatima Siddique, Sanna Korpela, Elina Mäntylä, Teemu O Ihalainen, Katri Kaukinen, Katriina Aalto-Setälä, Katri Lindfors, Kati Juuti-Uusitalo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. NF2 is Essential for Human Endoderm Development.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. iPSC-derived cells for whole liver bioengineering.Frontiers in bioengineering and biotechnology · 2024
    Review
  5. 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

9 authors at 1 institution in 1 country.

Jaakko SaariFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Fatima SiddiqueFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Sanna KorpelaFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Elina MäntyläFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.ORCID 0000-0002-8681-8772
Teemu O IhalainenFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Katri KaukinenFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Katriina Aalto-SetäläFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Katri LindforsFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.ORCID 0000-0001-7417-5151
Kati Juuti-UusitaloFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.ORCID 0000-0003-2275-5562
Tampere University · FI

Funding

Mary and George C. Ehrnrooth foundation year 2021
6 · The paper itself

Abstract

The small intestinal epithelium has an important role in nutrition, but also in drug absorption and metabolism. There are a few two-dimensional (2D) patient-derived induced pluripotent stem cell (iPSC)-based intestinal models enabling easy evaluation of transcellular transport. It is known that animal-derived components induce variation in the experimental outcomes. Therefore, we aimed to refine the differentiation protocol by using animal-free components. More specifically, we compared maturation of 2D-cultured iPCSs toward small intestinal epithelial cells when cultured either with or without serum, and either on Geltrex or on animal-free, recombinant laminin-based substrata. Differentiation status was characterized by qPCR, immunofluorescence imaging, and functionality assays. Our data suggest that differentiation toward definitive endoderm is more efficient without serum. Both collagen- and recombinant laminin-based coating supported differentiation of definitive endoderm, posterior definitive endoderm, and small intestinal epithelial cells from iPS-cells equally well. Small intestinal epithelial cells differentiated on recombinant laminin exhibited slightly more enterocyte specific cellular functionality than cells differentiated on Geltrex. Our data suggest that functional small intestinal epithelial cells can be generated from iPSCs in serum-free method on xeno-free substrata. This method is easily converted to an entirely xeno-free method.

Indexed as

AnimalsCell Culture TechniquesCell DifferentiationCell LineCells, CulturedEpithelial CellsHumansInduced Pluripotent Stem CellsIntestinal Mucosa2D iPSC-SIECinduced pluripotent stem celliPSCiPSC-SIECKO-SRrecombinant lamininserum-free culturesmall intestinal epithelial cell

Identifiers

PMID35163236
PMCPMC8835723
OpenAlexW4210324724

What OpenQuestion holds

Textmetadata
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.