Evidence map›Paper›PMID 40682140›Full record

ArticleBMC research notes2025

Efficient and simple protocol for mechanical isolation of foreskin-derived primary human dermal fibroblasts for replicative senescence studies.

Astrid Feinisa Khairani, Nayla Majeda Alfarafisa, Yoan Chou, Widad Aghnia Shalannandia, Maiko Ikezawa, Achadiyani Achadiyani, Nur Atik

Abstract read
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Article in BMC research notes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Astrid Feinisa KhairaniDepartment of Biomedical Sciences, Faculty of Medicine, Universitas Padjadjaran, Bandung, West Java, Indonesia. astrid.khairani@unpad.ac.id.
Nayla Majeda AlfarafisaDepartment of Biomedical Sciences, Faculty of Medicine, Universitas Padjadjaran, Bandung, West Java, Indonesia.
Yoan ChouGraduate School of Master Program in Anti Aging and Aesthetic Medicine, Faculty of Medicine, Universitas Padjadjaran, Bandung, West Java, Indonesia.
Widad Aghnia ShalannandiaBiomedical Science Master Program, Faculty of Medicine, Universitas Padjadjaran, Bandung, West Java, Indonesia.
Maiko IkezawaDepartment of Anatomy and Cell Biology, Graduate School of Medicine, Gunma University, Gunma, Japan.
Achadiyani AchadiyaniDepartment of Biomedical Sciences, Faculty of Medicine, Universitas Padjadjaran, Bandung, West Java, Indonesia.
Nur AtikDepartment of Biomedical Sciences, Faculty of Medicine, Universitas Padjadjaran, Bandung, West Java, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn efficient and reproducible protocol was developed for the mechanical isolation of human dermal fibroblasts (HDFs) from the foreskin, providing a practical alternative to enzymatic methods. This protocol could be easily performed with limited resources by reducing the need for expensive reagents and complex procedures. Viable cells were successfully subcultured repeatedly for cellular senescence studies, with reproducibility ensured through a detailed description.

resultsThis mechanical isolation method successfully generated HDFs with elongated spindle-shaped morphological characteristics that expressed the ACTIN protein, VIMENTIN protein, and SERPINH1 gene. HDFs survived through passage 8 (P8) during repeated subculturing.

conclusionsThe mechanical isolation protocol efficiently yields primary HDFs from the foreskin and supports replicative senescence up to passage 8 (P8). It can be applied to intrinsic skin aging studies, particularly in resource-limited settings.

Indexed as

Cell SeparationCellular SenescenceDermisFibroblastsForeskinActinsCells, CulturedHumansMaleVimentinActinsVimentinDermal fibroblastFibroblast-derived humanMechanical isolationPrimary cell cultureReplicative senescence

Identifiers

PMID40682140
PMCPMC12275237

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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.