Evidence map›Paper›PMID 39567419›Full record

ArticleGenes & genomics2025

The facilitated osteogenic differentiation by extracellular proline treatment in in vitro cell cultivation using MC3T3E1 and hPDLF.

Sung-Ho Son, Anna Kim, Je-Hee Jang, Elina Pokharel, Bandana Rana, Tae-Young Kim, Jae-Hee Lee, Seo-Young An, Chang-Hyeon An, Kwang-Kyun Park and 3 more

Abstract read
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In one paragraph

Article in Genes & genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Sung-Ho Son *Department of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Anna Kim *Department of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Je-Hee JangDepartment of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Elina PokharelDepartment of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Bandana RanaDepartment of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Tae-Young KimDepartment of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Jae-Hee LeeDepartment of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Seo-Young AnDepartment of Oral and Maxillofacial Radiology, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Chang-Hyeon AnDepartment of Oral and Maxillofacial Radiology, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Kwang-Kyun ParkProfessor Emeritus Department of Oral Biology, College of Dentistry, Yonsei University, Seoul, Korea.
Tae-Yub KwonDepartment of Dental Biomaterials, School of Dentistry, Kyungpook National University, Daegu, Korea.
Jae-Young KimDepartment of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea. jykim91@knu.ac.kr.ORCID 0000-0002-6752-5683
Wern-Joo SohnCollege of K-Biohealth, Daegu Haany University, Gyeongsan, Korea. wjsohn@dhu.ac.kr.

Funding

National Research Foundation of Korea NRF-2018R1D1A1A02086098
6 · The paper itself

Abstract

Proline is a major substrate in collagen biosynthesis and is required for collagen molecule formations. However, detailed explanations of the molecular basis through which proline functions in collagen biosynthesis have yet to be provided. Thus, genome-wide screening was employed to elucidate these in the pre-osteoblastic MC3T3-E1 and human periodontal ligament fibroblast (hPDLF) cell lines. Indeed, both cell lines represent important sources for collagen biosynthesis and tissue regeneration in the dental region, specifically treating extracellular proline during cultivations. The altered gene expression patterns were identified, and the precise expression patterns were confirmed by microarray. Cell viability and osteogenic differentiation patterns were examined using a range of experimental methods, such as the MTS assay, ALP staining, ARS staining, and collagen (COL)-type1A ELISA. Overall, we revealed a cell line-specific function of exogenous proline in collagen biosynthesis during osteogenic differentiation conditions with the candidate signaling pathways. These putative signaling networks could represent plausible answers to understanding collagen biosynthesis for regenerating connective tissues such as skin, muscle, and bone.

Indexed as

Cell DifferentiationFibroblastsOsteoblastsOsteogenesisPeriodontal LigamentProlineAnimalsCell LineCollagenHumansMiceCollagenProlineCollagen biosynthesisGenome-wide screeningOsteogenic differentiationProlineTCA cycle

Identifiers

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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.