Evidence map›Paper›PMID 28852702›Full record

ArticleACS central science2017

A Nano-In-Micro System for Enhanced Stem Cell Therapy of Ischemic Diseases.

Hai Wang, Pranay Agarwal, Yichao Xiao, Hao Peng, Shuting Zhao, Xuanyou Liu, Shenghua Zhou, Jianrong Li, Zhenguo Liu, Xiaoming He

Abstract read
In one paragraph

Article in ACS central science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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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

10 authors.

Hai WangDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Pranay AgarwalDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Yichao XiaoDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Hao PengDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Shuting ZhaoDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Xuanyou LiuDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Shenghua ZhouDepartment of Burns and Plastic Surgery, The Third Xiangya Hospital and Department of Cardiology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410013, P.R. China.
Jianrong LiDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Zhenguo LiuDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.
Xiaoming HeDepartment of Biomedical Engineering, Comprehensive Cancer Center, Davis Heart and Lung Research Institute, and Division of Cardiovascular Medicine, and Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio 43210, United States.

Funding

A novel lactic acid bacteria-based norovirus vaccineR01AI123661 · NIAID · OHIO STATE UNIVERSITY · PI BOYAKA, PROSPER N, HE, XIAOMING · 2016 to 2020
$3.0M
Oxidized Low-density Lipoprotein Impairs Bone Marrow Stem Cell SurvivalR01HL124122 · NHLBI · OHIO STATE UNIVERSITY · PI LIU, ZHENGUO, ZHU, HUA · 2015 to 2018
$2.1M
Ambient fine particulate matter and bone marrow stem cellsR01ES026200 · NIEHS · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, ZHENGUO · 2016 to 2020
$1.7M
Microfluidic encapsulation of ovarian follicles for biomimetic 3D culture andcryopreservationR01EB023632 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI HE, XIAOMING · 2017 to 2020
$1.6M
NHLBI NIH HHS R01 HL124122NIAID NIH HHS R01 AI123661NIBIB NIH HHS R01 EB023632NIEHS NIH HHS R01 ES026200
6 · The paper itself

Abstract

Stem cell therapy holds great potential for treating ischemic diseases. However, contemporary methods for local stem cell delivery suffer from poor cell survival/retention after injection. We developed a unique multiscale delivery system by encapsulating therapeutic agent-laden nanoparticles in alginate hydrogel microcapsules and further coentrapping the nano-in-micro capsules with stem cells in collagen hydrogel. The multiscale system exhibits significantly higher mechanical strength and stability than pure collagen hydrogel. Moreover, unlike nanoparticles, the nano-in-micro capsules do not move with surrounding body fluid and are not taken up by the cells. This allows a sustained and localized release of extracellular epidermal growth factor (EGF), a substance that could significantly enhance the proliferation of mesenchymal stem cells while maintaining their multilineage differentiation potential via binding with its receptors on the stem cell surface. As a result, the multiscale system significantly improves the stem cell survival at 8 days after implantation to ∼70% from ∼4-7% for the conventional system with nanoparticle-encapsulated EGF or free EGF in collagen hydrogel. After injecting into the ischemic limbs of mice, stem cells in the multiscale system facilitate tissue regeneration to effectively restore ∼100% blood perfusion in 4 weeks without evident side effects.

Identifiers

PMID28852702
PMCPMC5571461

What OpenQuestion holds

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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.