Evidence map›Paper›PMID 42756670›Full record

ArticleBone reports2026

Unidirectional porous beta-tricalcium phosphate supports three-dimensional osteogenic differentiation of human iPS cells without surface coating.

Akihito Kawai, Yusuke Inagaki, Kensuke Okamura, Yoshinobu Hyakuda, Masakazu Okamoto, Munehiro Ogawa, Akira Kido, Yasuhito Tanaka, Kenji Kawamura

Abstract read
In one paragraph

Article in Bone reports, 2026. 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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0citing papers in PubMed
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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

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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.

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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

9 authors.

Akihito KawaiDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara, Japan.
Yusuke InagakiDepartment of Rehabilitation Medicine, Nara Medical University, Kashihara, Nara, Japan.
Kensuke OkamuraDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara, Japan.
Yoshinobu HyakudaDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara, Japan.
Masakazu OkamotoDepartment of Rehabilitation Medicine, Nara Medical University, Kashihara, Nara, Japan.
Munehiro OgawaDepartment of Sports Medicine, Nara Medical University, Kashihara, Nara, Japan.
Akira KidoDepartment of Rehabilitation Medicine, Nara Medical University, Kashihara, Nara, Japan.
Yasuhito TanakaDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara, Japan.
Kenji KawamuraDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beta-tricalcium phosphate (βTCP) is widely used as a bone graft substitute, but it lacks intrinsic osteogenic cells. Human induced pluripotent stem cells (iPSCs) are a promising cell source for bone regeneration; however, the suitability of clinically available, uncoated βTCP as a scaffold for iPSC osteogenic differentiation remains unclear. We compared interconnected porous and unidirectional porous βTCP combined with either negative-pressure or atmospheric-pressure seeding. Metabolic activity was assessed using a CCK-8 assay, and the selected condition was further evaluated by RT-qPCR, scanning electron microscopy, and immunofluorescence staining during osteogenic induction. In vivo osteogenic progression was examined after subcutaneous transplantation into immunodeficient rodents. Negative-pressure seeding was associated with lower metabolic activity, whereas atmospheric-pressure seeding onto unidirectional porous βTCP yielded the highest values among the tested conditions. Under this condition, undifferentiated markers decreased after osteogenic induction, while osteoblast- and osteocyte-related genes showed time-dependent changes consistent with osteogenic lineage progression. Scanning electron microscopy demonstrated cell attachment and three-dimensional extension within the oriented pores, and immunofluorescence staining showed increasing type I collagen deposition during culture. After transplantation, human cell-derived RNA remained detectable, and several osteogenic markers increased over time. These findings indicate that clinically available, uncoated unidirectional porous βTCP can support the survival and osteogenic differentiation of human iPSCs in the absence of additional scaffold coating. This system may provide a simple platform for further studies of iPSC-based bone regenerative strategies.

Indexed as

Bone regenerationHuman induced pluripotent stem cellsOsteogenic differentiationUnidirectional porous scaffoldβ-Tricalcium phosphate

Identifiers

PMID42756670
PMCPMC13584143

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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.