Evidence map›Paper›PMID 31998133›Full record

ArticleFrontiers in pharmacology2019

Using Recombinant Human Collagen With Basic Fibroblast Growth Factor to Provide a Simulated Extracellular Matrix Microenvironment for the Revascularization and Attachment of Islets to the Transplantation Region.

Qunyan Zhu, Cuitao Lu, Xuan Jiang, Qing Yao, Xue Jiang, Zhiwei Huang, Yina Jiang, Lei Peng, Hongxing Fu, Yingzheng Zhao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
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  6. An Overview of Engineered Hydrogel-Based Biomaterials for ImprovedFrontiers in bioengineering and biotechnology · 2021
    Review
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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 at 2 institutions in 1 country.

Qunyan ZhuCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Cuitao LuCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Xuan JiangCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Qing YaoCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Xue JiangCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Zhiwei HuangCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Yina JiangCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Lei PengCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Hongxing FuCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Yingzheng ZhaoCollege of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Wenzhou Medical University · CNHainan Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Islet transplantation is considered a potential therapeutic option to reverse diabetes. The pancreatic basement membrane contains a variety of extracellular matrix (ECM) proteins. The abundant ECM is essential for the survival of transplanted islets. However, the ECM proteins necessary for maintaining islet vascularization and innervation are impaired by enzymatic digestion in the isolation process before islet transplantation, leading to destruction of islet microvessels. These are the primary concern and major barrier for long-term islet survival and function. Thus, it is crucial to create an appropriate microenvironment for improving revascularization and islet function to achieve better transplantation outcome. Given the importance of the presence of ECM proteins for islets, we introduce recombinant human collagen (RHC) to construct a simulated ECM microenvironment. To accelerate revascularization and reduce islet injury, we add basic fibroblast growth factor (bFGF) to RHC, a growth factor that has been shown to promote angiogenesis. In order to verify the outcome, islets were treated with RHC combination containing bFGF and then implanted into kidney capsule in type 1 diabetic mouse models. After transplantation, 30-day-long monitoring displayed that 16 mg-60 ng RHC-bFGF group could serve as superior transplantation outcome. It reversed the hyperglycemia condition in host rapidly, and the OGTT (oral glucose tolerance test) showed a similar pattern with the control group. Histological assessment showed that 16 mg-60 ng RHC-bFGF group attenuated apoptosis, promoted cellular proliferation, triggered vascularization, and inhibited inflammation reaction. In summary, this work demonstrates that application of 16 mg-60 ng RHC-bFGF and islets composite enhance the islet survival, function, and long-term transplantation efficiency.

Indexed as

basic fibroblast growth factor (bFGF)diabetesislet–matrix attachmentsislet transplantationrecombinant human collagen (RHC)

Identifiers

PMID31998133
PMCPMC6965329
OpenAlexW2998876028

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.