Evidence map›Paper›PMID 42409877›Full record

ArticleScientific reports2026

Evaluating the impact of PBM wavelengths on CTGF-driven tenogenic differentiation of ADMSCs through multi-level analyses.

Amarachi Albert, Heidi Abrahamse, Anine Crous

Abstract read
In one paragraph

Article in Scientific 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.

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

3 authors.

Amarachi AlbertLaser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein, 2028, South Africa.
Heidi AbrahamseLaser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein, 2028, South Africa.
Anine CrousLaser Research Centre, Faculty of Health Sciences, University of Johannesburg, P.O. Box 17011, Doornfontein, 2028, South Africa. acrous@uj.ac.za.

Funding

National Research Foundation 98337National Research Foundation TTK2205035996South African Medical Research Council 57050University Research Council 2024URC00813
6 · The paper itself

Abstract

Evaluating the Impact of PBM Wavelengths on CTGF-Driven Tenogenic Differentiation of ADMSCs Through Multi-Level Analyses" studied the effects of photobiomodulation (PBM) on the tenogenic differentiation of adipose-derived mesenchymal stem cells (ADMSCs) stimulated with connective tissue growth factor (CTGF) using a range of wavelengths (525 nm, 825 nm, and their combination) and fluences (5 and 10 J/cm²). Gene expression (qPCR for COL1A1, COL3A1, TNMD, TNC, BGN, and SMAD3), morphological alterations (Giemsa staining), metabolic activity (ATP test), and cytotoxicity (LDH release) were all evaluated using a multi-level experimental design. On Day 5, ATP production was significantly enhanced without cytotoxicity by using dual-wavelength PBM at 5 J/cm². On the other hand, metabolic activity was decreased but membrane integrity was preserved at a higher fluence of 10 J/cm². By Day 10, the spindle-shaped morphology and cellular alignment were more apparent in Giemsa-stained cells that had been exposed to dual-wavelength PBM. A synergistic impact in promoting tendon-specific lineage commitment was shown by gene expression analysis, which showed substantial elevation of critical tenogenic markers under dual-wavelength PBM at 5 J/cm². Taken together, these results show that PBM works best when the wavelength and dosage are optimized, and they provide credence to the idea that PBM might be a non-invasive way to boost tendon regeneration procedures that use stem cells.

Indexed as

Adipose-derived mesenchymal stem cells (ADMSCs)ATP assayConnective tissue growth factor (CTGF)Extracellular matrix (ECM)LDH assayPhotobiomodulation (PBM)QPCRStem cell therapyTendon regenerationTenogenic differentiation

Identifiers

PMID42409877
PMCPMC13638455

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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.