Evidence map›Paper›PMID 25818411›Full record

ReviewBiomaterials2015

On human pluripotent stem cell control: The rise of 3D bioengineering and mechanobiology.

Yue Shao, Jianming Sang, Jianping Fu

Abstract readReview
In one paragraph

Review in Biomaterials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
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  4. Cell-extracellular matrix mechanotransduction in 3D.Nature reviews. Molecular cell biology · 2023
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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

3 authors at 1 institution in 1 country.

Yue ShaoDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Jianming SangDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Jianping FuDepartment of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: jpfu@umich.edu.
University of Michigan · US

Funding

Microfluidic Functional Immunophenotyping of Pediatric Patients Following CardiopR01HL119542 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CORNELL, TIMOTHY T, FU, JIANPING · 2014 to 2017
$2.7M
Acoustic tweezing cytometry: technology development and stem cell applicationsR01EB019436 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DENG, CHERI X, FU, JIANPING · 2015 to 2018
$1.9M
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
NHLBI NIH HHS R01 HL119542NHLBI NIH HHS R21 HL114011NIBIB NIH HHS R01 EB019436NIBIB NIH HHS R21 EB017078
6 · The paper itself

Abstract

Human pluripotent stem cells (hPSCs) provide promising resources for regenerating tissues and organs and modeling development and diseases in vitro. To fulfill their promise, the fate, function, and organization of hPSCs need to be precisely regulated in a three-dimensional (3D) environment to mimic cellular structures and functions of native tissues and organs. In the past decade, innovations in 3D culture systems with functional biomaterials have enabled efficient and versatile control of hPSC fate at the cellular level. However, we are just at the beginning of bringing hPSC-based regeneration and development and disease modeling to the tissue and organ levels. In this review, we summarize existing bioengineered culture platforms for controlling hPSC fate and function by regulating inductive mechanical and biochemical cues coexisting in the synthetic cell microenvironment. We highlight recent excitements in developing 3D hPSC-based in vitro tissue and organ models with in vivo-like cellular structures, interactions, and functions. We further discuss an emerging multifaceted mechanotransductive signaling network--with transcriptional coactivators YAP and TAZ at the center stage--that regulate fates and behaviors of mammalian cells, including hPSCs. Future development of 3D biomaterial systems should incorporate dynamically modulated mechanical and chemical properties targeting specific intracellular signaling events leading to desirable hPSC fate patterning and functional tissue formation in 3D.

Indexed as

Biocompatible MaterialsBiomechanical PhenomenaBiomedical EngineeringCell Culture TechniquesCell DifferentiationEquipment DesignHumansPluripotent Stem CellsTissue EngineeringBiocompatible MaterialsBioengineeringDevelopmentHuman disease modelingHuman pluripotent stem cellsMechanobiologyRegenerative medicine

Identifiers

PMID25818411
PMCPMC4379448
OpenAlexW2123079531

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.