Evidence map›Paper›PMID 39329311›Full record

ArticleJournal of peptide science : an official publication of the European Peptide Society2025

RGD-functionalised self-assembling peptide hydrogel induces a proliferative profile in human osteoblasts in vitro.

Luis A Castillo-Díaz, Julie E Gough, Aline F Miller, Alberto Saiani

Abstract read
In one paragraph

Article in Journal of peptide science : an official publication of the European Peptide Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. RGD-functionalised self-assembling peptide hydrogel induces a proliferative profile in human osteoblasts in vitro.Journal of peptide science : an official publication of the European Peptide Society · 2025
    Article
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

4 authors.

Luis A Castillo-DíazSchool of Chemical Engineering & Manchester Institute of Biotechnology, The University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0001-9944-9040
Julie E GoughSchool of Materials & Henry Royce Institute, The University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0002-1270-0616
Aline F MillerSchool of Chemical Engineering & Manchester Institute of Biotechnology, The University of Manchester, Manchester, UK.
Alberto SaianiDivision of Pharmacy and Optometry & Manchester Institute of Biotechnology, The University of Manchester, Manchester, UK.ORCID https://orcid.org/0000-0002-5504-8306

Funding

CONAHCYT MéxicoEPSRC Early Career Research Fellowship EP/K016210/1MRC Acellular/Smart Materials -3D Architecture: UK RMP Hub MR/R015651/1
6 · The paper itself

Abstract

Self-assembling peptide hydrogels (SAPHs) have been used in the past decade as reliable three-dimensional (3D) synthetic scaffolds for the culture of a variety of mammalian cells in vitro. Thanks to their versatile physicochemical properties, they allow researchers to tailor the hydrogel properties, including stiffness and functionality to the targeted cells and cells' behaviour. One of the advantages of using SAPH scaffolds is the ease of functionalisation. In the present work, we discuss the effect that functionalising the FEFEFKFK (F, phenylalanine; K, lysine; and E, glutamic acid) hydrogel scaffold using the cell-binding RGDS (fibronectin - R, arginine; G, glycine; D, aspartic acid; S, serine) epitope affects the material properties as well as the function of encapsulated human osteoblast cells. RGDS functionalisation resulted in cells adopting an elongated morphology, suggesting attachment and increased proliferation. While this led to higher cell viability, it also resulted in a decrease in extra-cellular matrix (ECM) protein production as well as a decrease in calcium ion deposition, suggesting lower mineralisation capabilities. The work clearly shows that SAPHs are a flexible platform that allow the modification of scaffolds in a controlled manner to investigate cell-material interactions.

Indexed as

Cell ProliferationHydrogelsOligopeptidesOsteoblastsCells, CulturedCell SurvivalHumansPeptidesTissue Scaffoldsarginyl-glycyl-aspartic acidHydrogelsOligopeptidesPeptidescalcium depositionhuman osteoblastshydrogelsRGDself‐assembling peptides

Identifiers

PMID39329311
PMCPMC11669940

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.