Evidence map›Paper›PMID 36294410›Full record

ArticleJournal of clinical medicine2022

The Role of Genetically Modified Human Feeder Cells in Maintaining the Integrity of Primary Cultured Human Deciduous Dental Pulp Cells.

Natsumi Ibano, Emi Inada, Shinji Otake, Yuki Kiyokawa, Kensuke Sakata, Masahiro Sato, Naoko Kubota, Hirofumi Noguchi, Yoko Iwase, Tomoya Murakami and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 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 48% 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, 1 citations in OpenAlex.

  1. Review
  2. Review
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

16 authors at 5 institutions in 1 country.

Natsumi IbanoDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.
Emi InadaDepartment of Pediatric Dentistry, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.
Shinji OtakeDivision of Pediatric Dentistry, Department of Oral Health and Development Sciences, Tohoku University Graduate School of Dentistry, Sendai 980-8575, Japan.
Yuki KiyokawaDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.ORCID 0000-0001-8406-130X
Kensuke SakataDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.
Masahiro SatoDepartment of Genome Medicine, National Center for Child Health and Development, Tokyo 157-8535, Japan.ORCID 0000-0003-1334-2950
Naoko KubotaDepartment of Pediatric Dentistry, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.
Hirofumi NoguchiDepartment of Regenerative Medicine, Graduate School of Medicine, University of the Ryukyus, Nishihara 903-0215, Japan.ORCID 0000-0002-0880-6805
Yoko IwaseDepartment of Dentistry for the Disabled, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.
Tomoya MurakamiDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.
Tadashi SawamiDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.
Yoshito KakiharaDivision of Dental Pharmacology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.
Takeyasu MaedaCenter for Advanced Oral Science, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.ORCID 0000-0001-5317-7510
Miho TerunumaDivision of Oral Biochemistry, Faculty of Dentistry, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.ORCID 0000-0003-1876-9726
Yutaka TeraoDivision of Microbiology and Infectious Diseases, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.ORCID 0000-0002-4450-5583
Issei SaitohDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho-shi 501-0296, Japan.ORCID 0000-0002-7451-0666
Asahi University · JPNiigata University · JPKagoshima University · JPTohoku University · JPUniversity of the Ryukyus · JP

Funding

Grants-in-Aid for Scientific Research 15K07695Grants-in-Aid for Scientific Research 21K10165Grants-in-Aid for Scientific Research 22H03277Grants-in-Aid for Scientific Research 22K17081Grants-in-Aid for Scientific Research 26670883
6 · The paper itself

Abstract

Tissue-specific stem cells exist in tissues and organs, such as skin and bone marrow. However, their pluripotency is limited compared to embryonic stem cells. Culturing primary cells on plastic tissue culture dishes can result in the loss of multipotency, because of the inability of tissue-specific stem cells to survive in feeder-less dishes. Recent findings suggest that culturing primary cells in medium containing feeder cells, particularly genetically modified feeder cells expressing growth factors, may be beneficial for their survival and proliferation. Therefore, the aim of this study was to elucidate the role of genetically modified human feeder cells expressing growth factors in maintaining the integrity of primary cultured human deciduous dental pulp cells. Feeder cells expressing leukemia inhibitory factor, bone morphogenetic protein 4, and basic fibroblast growth factor were successfully engineered, as evidenced by PCR. Co-culturing with mitomycin-C-treated feeder cells enhanced the proliferation of newly isolated human deciduous dental pulp cells, promoted their differentiation into adipocytes and neurons, and maintained their stemness properties. Our findings suggest that genetically modified human feeder cells may be used to maintain the integrity of primary cultured human deciduous dental pulp cells.

Indexed as

dental pulp cellsfeeder cellsgenetic engineeringhuman deciduous teethstem cells

Identifiers

PMID36294410
PMCPMC9605397
OpenAlexW4306385956

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.