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Study 6 of 13GHK-Cu literatureeuropepmc · Observational2026

Hierarchical regulation and mechanism of "open-hollow-fibrous network" structures: Osteogenic-angiogenic coupling responses of poly(γ-benzyl-L-glutamate) microspheres.

The study suggests that GHK-Cu functionalized microspheres could enhance bone tissue engineering efforts, but further research is needed to confirm these findings in vivo.

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Where it sits

this study against the rest of the ghk-cu corpus
6
Preclinical
7
Observational · this one
0
Open-label
0
Randomised
0
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Summary and findings

This study investigated the fabrication and biofunctionality of polypeptide microspheres (PBLG-GCu HNMs) for bone tissue engineering. The microspheres were designed to enhance osteogenic and angiogenic responses in bone marrow mesenchymal stem cells (BMSCs). Key findings included significant increases in osteogenic gene expression compared to non-functionalized microspheres.

How much of this paper we could read: full text read (0.70). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Runx2 expression increased by 1.61-fold, OPN by 3.53-fold, and OCN by 2.29-fold compared to non-functionalized PBLG HNMs.2026

Abstract

The authors’ words, as europepmc supplied them

Biomimetic fibrous microspheres with a high specific surface area hold substantial promise for bone tissue engineering. In this study, asymmetric open-hollow nanofibrous microspheres (HNMs) were fabricated from polypeptide poly(γ-benzyl-L-glutamate) (PBLG) via a combination of emulsion and thermally induced phase separation, yielding PBLG HNMs. To further impart biofunctionality, the copper peptide (GHK-Cu) was covalently grafted onto the microspheres to obtain osteoinductive and pro-angiogenic PBLG-GCu HNMs. The optimized microspheres exhibited an average diameter of 372 ± 102 μm, which is suitable for injectability, and an opening size of 219 ± 53 μm, enabling efficient cellular infiltration. The internal surface featured an interconnected nanofibrous network with a fiber diameter of 417 ± 78 nm, mimicking the extracellular matrix (ECM) microenvironment and providing abundant cell-interactive sites. Live/Dead staining and CCK-8 assays confirmed the cytocompatibility of the PBLG-GCu HNMs. Compared with non-functionalized PBLG HNMs, PBLG-GCu HNMs enhanced bone marrow mesenchymal stem cell (BMSC) mineralization and upregulated osteogenic gene expression, with Runx2, OPN, and OCN expression increased by 1.61-, 3.53-, and 2.29-fold, respectively. In addition, the tube formation assay verified robust angiogenic stimulation. Overall, the PBLG-GCu HNMs integrated hierarchical structural biomimicry with dual osteogenic-angiogenic bioactivity, exhibiting great potential as injectable scaffolds for repairing irregular bone defects.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Key findings

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Limitations

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Elsewhere in the GHK-Cu corpus

DMining triggers extensive additional deforestation in sub-Saharan Africa.Nature · 2026DOrbital magnetoresistance in the antiferromagnet CoO driven by dynamic orbital angular momentum.Science (New York, N.Y.) · 2026DSurface-dominant transport in Weyl semimetal NbAs nanowires for next-generation interconnects.Science (New York, N.Y.) · 2026CThe GHK-Cu delays aging in Caenorhabditis elegans via coordinated regulation of mitochondrial function and activation of DAF-16/SKN-1 pathways.Biogerontology · 2026 · n=200 · Not reported in abstract.AnimalCHierarchical regulation and mechanism of "open-hollow-fibrous network" structures: Osteogenic-angiogenic coupling responses of poly(γ-benzyl-L-glutamate) microspheres.PubMed · 2026 · Runx2 expression increased by 1.61-fold, OPN by 3.53-fold, and OCN by 2.29-fold compared to non-functionalized PBLG HNMs.In vitroCMiddle-aged mice treated with GHK-Cu peptide administered intraperitoneally or intranasally show behavioral rescue but divergent hippocampal aging programsbiorxiv-preprint · 2026 · IN treatment increased synaptophysin in females (P < 0.001).Animal