Evidence map›Paper›PMID 37999192›Full record

ArticleBiomimetics (Basel, Switzerland)2023

Detergent-Based Decellularization for Anisotropic Cardiac-Specific Extracellular Matrix Scaffold Generation.

Te-An Chen, Dhavan Sharma, Wenkai Jia, Donggi Ha, Kun Man, Jianhua Zhang, Yong Yang, Yuxiao Zhou, Timothy J Kamp, Feng Zhao

Abstract read
In one paragraph

Article in Biomimetics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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. Review
  2. Article
  3. Review
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  5. 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

10 authors.

Te-An ChenDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0009-0007-1198-8068
Dhavan SharmaDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Wenkai JiaDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Donggi HaDepartment of Mechanical Engineering, Texas A&M University, College Station, TX 77843, USA.
Kun ManDepartment of Biomedical Engineering, University of North Texas, Denton, TX 76203, USA.
Jianhua ZhangStem Cell and Regenerative Medicine Center, University of Wisconsin-Madison, Madison, WI 53705, USA.
Yong YangDepartment of Biomedical Engineering, University of North Texas, Denton, TX 76203, USA.ORCID 0000-0003-4305-8029
Yuxiao ZhouDepartment of Mechanical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0001-5143-8967
Timothy J KampStem Cell and Regenerative Medicine Center, University of Wisconsin-Madison, Madison, WI 53705, USA.ORCID 0000-0003-2103-7876
Feng ZhaoDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0003-4138-9027

Funding

Integrated Cellular and Tissue Engineering for Ischemic Heart DiseaseU01HL134764 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BURSAC, NENAD, KAMP, TIMOTHY J. · 2016 to 2022
$7.7M
Engineered Anisotropic and Vascularized Human Cardiac PatchR01HL146652 · NHLBI · TEXAS ENGINEERING EXPERIMENT STATION · PI ZHAO, FENG · 2020 to 2023
$1.4M
Optic-nerve-head (ONH) Chips for Glaucomatous NeurodegenerationR15EY033967 · NEI · UNIVERSITY OF NORTH TEXAS · PI YANG, YONG · 2022 to 2022
$463k
NEI NIH HHS R15 EY033967NHLBI NIH HHS R01 HL146652NHLBI NIH HHS U01 HL134764
6 · The paper itself

Abstract

Cell-derived extracellular matrix (ECM) has become increasingly popular in tissue engineering applications due to its ability to provide tailored signals for desirable cellular responses. Anisotropic cardiac-specific ECM scaffold decellularized from human induced pluripotent stem cell (hiPSC)-derived cardiac fibroblasts (hiPSC-CFs) mimics the native cardiac microenvironment and provides essential biochemical and signaling cues to hiPSC-derived cardiomyocytes (hiPSC-CMs). The objective of this study was to assess the efficacy of two detergent-based decellularization methods: (1) a combination of ethylenediaminetetraacetic acid and sodium dodecyl sulfate (EDTA + SDS) and (2) a combination of sodium deoxycholate and deoxyribonuclease (SD + DNase), in preserving the composition and bioactive substances within the aligned ECM scaffold while maximumly removing cellular components. The decellularization effects were evaluated by characterizing the ECM morphology, quantifying key structural biomacromolecules, and measuring preserved growth factors. Results showed that both treatments met the standard of cell removal (less than 50 ng/mg ECM dry weight) and substantially preserved major ECM biomacromolecules and growth factors. The EDTA + SDS treatment was more time-efficient and has been determined to be a more efficient method for generating an anisotropic ECM scaffold from aligned hiPSC-CFs. Moreover, this cardiac-specific ECM has demonstrated effectiveness in supporting the alignment of hiPSC-CMs and their expression of mature structural and functional proteins in in vitro cultures, which is crucial for cardiac tissue engineering.

Indexed as

cardiac-specific scaffoldcardiac tissue engineeringdecellularizationextracellular matrix

Identifiers

PMID37999192
PMCPMC10669368

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Registered trials

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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.