Evidence map›Paper›PMID 26053044›Full record

ArticleScientific reports2015

Cell proliferation by silk gut incorporating FGF-2 protein microcrystals.

Eiji Kotani, Naoto Yamamoto, Isao Kobayashi, Keiro Uchino, Sayaka Muto, Hiroshi Ijiri, Junji Shimabukuro, Toshiki Tamura, Hideki Sezutsu, Hajime Mori

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. 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
0.9field-weighted citation impact, top 26% 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.

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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.

Eiji Kotani1] Department of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan [2] Insect Biomedical Centre, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.
Naoto YamamotoDepartment of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.
Isao KobayashiTransgenic Silkworm Research Unit, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Keiro UchinoTransgenic Silkworm Research Unit, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Sayaka MutoDepartment of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.
Hiroshi IjiriDepartment of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.
Junji ShimabukuroDepartment of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.
Toshiki TamuraTransgenic Silkworm Research Unit, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Hideki SezutsuTransgenic Silkworm Research Unit, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Hajime Mori1] Department of Applied Biology, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan [2] Insect Biomedical Centre, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.
Kyoto Institute of Technology · JPInstitute of Agrobiological Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silk gut processed from the silk glands of the silkworm could be an ideal biodegradable carrier for cell growth factors. We previously demonstrated that polyhedra, microcrystals of Cypovirus 1 polyhedrin, can serve as versatile carrier proteins. Here, we report the generation of a transgenic silkworm that expresses polyhedrin together with human basic fibroblast growth factor (FGF-2) in its posterior silk glands to utilize silk gut as a proteinaceous carrier to protect and slowly release active cell growth factors. In the posterior silk glands, polyhedrin formed polyhedral microcrystals, and FGF-2 became encapsulated within the polyhedra due to a polyhedron-immobilization signal. Silk gut powder prepared from posterior silk glands containing polyhedron-encapsulated FGF-2 stimulated the phosphorylation of p44/p42 MAP kinase and induced the proliferation of serum-starved NIH3T3 cells by releasing bioactive FGF-2. Even after a one-week incubation at 25 °C, significantly higher biological activity of FGF-2 was observed for silk gut powder incorporating polyhedron-encapsulated FGF-2 relative to silk gut powder with non-encapsulated FGF-2. Our results demonstrate that posterior silk glands incorporating polyhedron-encapsulated FGF-2 are applicable to the preparation of biodegradable silk gut, which can protect and release FGF-2 that is produced in a virus- and serum-free expression system with significant application potential.

Indexed as

AnimalsAnimals, Genetically ModifiedBombyxCell LineCell ProliferationDrug CarriersFibroblast Growth Factor 2Gene ExpressionMiceMitogen-Activated Protein Kinase 1NIH 3T3 CellsPeptide FragmentsPhosphorylationReoviridaeSilkTranscription FactorsDrug CarriersFibroblast Growth Factor 2Mitogen-Activated Protein Kinase 1Peptide FragmentsSilkTranscription FactorsTumor Suppressor Protein p53WDR77 protein, mouse

Identifiers

PMID26053044
PMCPMC4459171
OpenAlexW2270232845

What OpenQuestion holds

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LicenceCC BY
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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.