Evidence map›Paper›PMID 26626176›Full record

ArticleStem cell reports2015

Lumen Formation Is an Intrinsic Property of Isolated Human Pluripotent Stem Cells.

Kenichiro Taniguchi, Yue Shao, Ryan F Townshend, Yu-Hwai Tsai, Cynthia J DeLong, Shawn A Lopez, Srimonta Gayen, Andrew M Freddo, Deming J Chue, Dennis J Thomas and 6 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

70 citing papers in PubMed, 121 citations in OpenAlex.

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  13. Primate amnion development.Development (Cambridge, England) · 2024
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10 more citing papers are in PubMed but not listed here.

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

16 authors at 1 institution in 1 country.

Kenichiro TaniguchiDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA. Electronic address: taniguch@med.umich.edu.
Yue ShaoDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Ryan F TownshendDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Yu-Hwai TsaiDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Cynthia J DeLongDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Shawn A LopezDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Srimonta GayenDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Andrew M FreddoDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Deming J ChueDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Dennis J ThomasDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Jason R SpenceDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Benjamin MargolisDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Sundeep KalantryDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Jianping FuDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
K Sue O'SheaDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Deborah L GumucioDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA. Electronic address: dgumucio@med.umich.edu.
University of Michigan–Ann Arbor · US

Funding

MICHIGAN MEDICAL SCIENTIST TRAINING PROGRAMT32GM007863 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, KATHLEEN L. · 1985 to 2024
$38.3M
University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
TRAINING PROGRAM IN ORGANOGENESIST32HD007505 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PASCA DI MAGLIANO, MARINA, SPENCE, JASON · 1997 to 2021
$6.9M
Morphogenesis of the fetal intestinal epitheliumR01DK089933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUMUCIO, DEBORAH L. · 2011 to 2019
$3.6M
Crumbs3 in epithelial polarity and ciliogenesisR01DK069605 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARGOLIS, BENJAMIN L · 2005 to 2013
$2.9M
Initiation of Epigenetic Transcriptional RegulationDP2OD008646 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KALANTRY, SUNDEEP · 2011 to 2011
$2.3M
Mechanisms of intestine developmentK01DK091415 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPENCE, JASON · 2011 to 2015
$700k
2012-Directed Differentiation of Stem Cells to Cardiomyocytes Using Optically ActR21HL114011 · NHLBI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HART, ANASTASIOS JOHN · 2013 to 2014
$429k
Ultrasound-mediated Directed Osteogenic Differentiation of Mesenchymal Stem CellsR21EB017078 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DENG, CHERI X, FU, JIANPING · 2014 to 2015
$428k
A novel Ezrin-dependent cell division drives villus formationF30DK100125 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FREDDO, ANDREW MICHAEL · 2013 to 2017
$103k
NHLBI NIH HHS R21 HL114011NHLBI NIH HHS R21-HL114011NIBIB NIH HHS R21 EB017078NIBIB NIH HHS R21-EB017078NICHD NIH HHS T32 HD007505NICHD NIH HHS T32-HD007505NIDDK NIH HHS F30 DK100125NIDDK NIH HHS F30-DK100125NIDDK NIH HHS K01 DK091415NIDDK NIH HHS K01-DK091415NIDDK NIH HHS P30 DK034933NIDDK NIH HHS R01 DK069605NIDDK NIH HHS R01 DK089933NIDDK NIH HHS R01-DK089933NIDDK NIH HHS R01-DK69605NIGMS NIH HHS T32 GM007863NIH HHS DP2 OD008646NIH HHS DP2-OD-008646-01
6 · The paper itself

Abstract

We demonstrate that dissociated human pluripotent stem cells (PSCs) are intrinsically programmed to form lumens. PSCs form two-cell cysts with a shared apical domain within 20 hr of plating; these cysts collapse to form monolayers after 5 days. Expression of pluripotency markers is maintained throughout this time. In two-cell cysts, an apical domain, marked by EZRIN and atypical PKCζ, is surrounded by apically targeted organelles (early endosomes and Golgi). Molecularly, actin polymerization, regulated by ARP2/3 and mammalian diaphanous-related formin 1 (MDIA), promotes lumen formation, whereas actin contraction, mediated by MYOSIN-II, inhibits this process. Finally, we show that lumenal shape can be manipulated in bioengineered micro-wells. Since lumen formation is an indispensable step in early mammalian development, this system can provide a powerful model for investigation of this process in a controlled environment. Overall, our data establish that lumenogenesis is a fundamental cell biological property of human PSCs.

Indexed as

ActinsAnimalsCell Culture TechniquesCell LineCell SeparationCell ShapeDogsHumansMicePluripotent Stem CellsActins

Identifiers

PMID26626176
PMCPMC4682207
OpenAlexW2178737443

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.