Evidence map›Paper›PMID 35481104›Full record

ArticleRSC advances2022

The restricted adhesion of bone marrow mesenchymal stem cells by stepped structures on surfaces of hydroxyapatite.

Jin Chen, Zhuo Huang, Fang Wang, Min Gong, Xueli Zhang, Yajing Wang, Zuquan Hu, Zhu Zeng, Yun Wang

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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

9 authors at 1 institution in 1 country.

Jin ChenKey Laboratory of Biology and Medical Engineering/Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Biology and Engineering, Guizhou Medical University Guiyang 550025 P. R. China huzuquan@gmc.edu.cn zengzhu@gmc.edu.cn wangyun@gmc.edu.cn.ORCID https://orcid.org/0000-0003-4757-512X
Zhuo HuangKey Laboratory of Biology and Medical Engineering/Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Biology and Engineering, Guizhou Medical University Guiyang 550025 P. R. China huzuquan@gmc.edu.cn zengzhu@gmc.edu.cn wangyun@gmc.edu.cn.
Fang WangKey Laboratory of Infectious Immune and Antibody Engineering of Guizhou Province, School of Basic Medical Sciences, Guizhou Medical University Guiyang 550025 P. R. China.
Min GongKey Laboratory of Biology and Medical Engineering/Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Biology and Engineering, Guizhou Medical University Guiyang 550025 P. R. China huzuquan@gmc.edu.cn zengzhu@gmc.edu.cn wangyun@gmc.edu.cn.
Xueli ZhangKey Laboratory of Infectious Immune and Antibody Engineering of Guizhou Province, School of Basic Medical Sciences, Guizhou Medical University Guiyang 550025 P. R. China.
Yajing WangThe Affiliated Stomatological Hospital of Guizhou Medical University, Guizhou Medical University Guiyang 550025 P. R. China.
Zuquan HuKey Laboratory of Biology and Medical Engineering/Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Biology and Engineering, Guizhou Medical University Guiyang 550025 P. R. China huzuquan@gmc.edu.cn zengzhu@gmc.edu.cn wangyun@gmc.edu.cn.
Zhu ZengKey Laboratory of Biology and Medical Engineering/Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Biology and Engineering, Guizhou Medical University Guiyang 550025 P. R. China huzuquan@gmc.edu.cn zengzhu@gmc.edu.cn wangyun@gmc.edu.cn.
Yun WangKey Laboratory of Biology and Medical Engineering/Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Biology and Engineering, Guizhou Medical University Guiyang 550025 P. R. China huzuquan@gmc.edu.cn zengzhu@gmc.edu.cn wangyun@gmc.edu.cn.ORCID https://orcid.org/0000-0002-0745-1723
Guiyang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, many researches have developed several strategies to design the surface structures of hydroxyapatite (HA), and have proved that the surface structures are pivotal in guiding the adhesion of bone marrow mesenchymal stem cells (BMSCs) as well as subsequent cellular behaviours. Most of these strategies, such as altering roughness and constructing surface patterning of HA, involve the construction of geometric topographies at the micro/nanoscale. However, besides geometric topographies, crystal defects are also important characteristics of surface structures and would alter many local physicochemical properties, which is critical for contact between cells and bioceramic surfaces. For the practical applications of crystal defects, a major hindrance is that crystal defects are usually unstable and easily eliminated during crystallization, which limits the large-scale fabrication of materials with crystal defects. In this work, given that stepped structures contain massive stable crystal defects on their step edges and kinks, we proposed a feasible and efficient method to fabricate HA dishes with stepped structures on their surfaces. First, plate-like HA mesocrystals were prepared from CaHPO

Identifiers

PMID35481104
PMCPMC9019829
OpenAlexW4225081543

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.