Evidence map›Paper›PMID 30144353›Full record

ArticleBiotechnology and bioengineering2018

Neonatal testis growth recreated in vitro by two-dimensional organ spreading.

Kazuaki Kojima, Hiroko Nakamura, Mitsuru Komeya, Hiroyuki Yamanaka, Yoshinori Makino, Yuki Okada, Haruhiko Akiyama, Nobuhito Torikai, Takuya Sato, Teruo Fujii and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 53 citations in OpenAlex.

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  17. Frontiers in cell and developmental biology · 2023
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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

12 authors at 5 institutions in 1 country.

Kazuaki KojimaLaboratory of Biopharmaceutical and Regenerative Sciences, Institute of Molecular Medicine and Life Science, Association of Medical Science, Yokohama City University, Yokohama, Japan.
Hiroko NakamuraDepartment of Mechanical Engineering, Tokai University, Hiratsuka, Japan.
Mitsuru KomeyaDepartment of Urology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Hiroyuki YamanakaDepartment of Urology, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Yoshinori MakinoLaboratory of Pathology and Development, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan.
Yuki OkadaLaboratory of Pathology and Development, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan.
Haruhiko AkiyamaDepartment of Orthopaedic Surgery, Graduate School of Medicine, Gifu University, Gifu, Japan.
Nobuhito TorikaiLaboratory of Biopharmaceutical and Regenerative Sciences, Institute of Molecular Medicine and Life Science, Association of Medical Science, Yokohama City University, Yokohama, Japan.
Takuya SatoLaboratory of Biopharmaceutical and Regenerative Sciences, Institute of Molecular Medicine and Life Science, Association of Medical Science, Yokohama City University, Yokohama, Japan.
Teruo FujiiInstitute of Industrial Science, University of Tokyo, Tokyo, Japan.
Hiroshi KimuraDepartment of Mechanical Engineering, Tokai University, Hiratsuka, Japan.
Takehiko OgawaLaboratory of Biopharmaceutical and Regenerative Sciences, Institute of Molecular Medicine and Life Science, Association of Medical Science, Yokohama City University, Yokohama, Japan.ORCID 0000-0002-1422-0317
Yokohama City University · JPThe University of Tokyo · JPTokai University · JPGifu University · JPTokyo University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ culture experiments can be hampered by central degeneration or necrosis due to the inadequate permeation of oxygen and nutrients, which deteriorates the function and growth of cultured tissues. In the current study, we aimed to overcome this limitation of organ culture through spreading the tissue two dimensionally on an agarose gel stand and molding into a disc shape by placing a ceiling of polydimethylsiloxane (PDMS) chip, which is highly oxygen permeable. By this, every part of the tissue can receive a sufficient supply of oxygen through PDMS as well as nutrients through the agarose gel below. This method not only prevented central necrosis of tissues, but also supported the tissue growth over time. In addition, such growth, as volume enlargement, could be easily measured. Under these conditions, we examined the effect of several factors on the growth of neonatal mouse testis, and found that follicle stimulating hormone (FSH) and insulin significantly promoted the growth. These results are in good agreement with previous in vivo reports. Notably, the growth achieved over 7 days in our in vitro system is almost comparable to, about 80% of, that observed in vivo. Thus, we successfully monitored the promotion of tissue growth beyond the limits of the conventional organ culture method. This extremely simple method could offer a unique platform to evaluate the growth as well as functional properties of organs, not only the testis but also others as well.

Indexed as

AnimalsAnimals, NewbornCells, CulturedDimethylpolysiloxanesLab-On-A-Chip DevicesMaleMiceMice, Inbred C57BLMice, Inbred ICRNylonsOrgan Culture TechniquesSertoli CellsTestisDimethylpolysiloxanesNylonspoly(dimethylsiloxane)-polyamide copolymerorgan culturePDMSSertoli cellstestistissue growth

Identifiers

PMID30144353
PMCPMC6283240
OpenAlexW2888225088

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.