# Identification of Novel Growth Factor Conjugated Nanofibers for Stimulation of Neuronal Growth

**Authors:** Yu‐Liang Tsai, Karla K. Rivera, Nayeong Jeon, Bernd Knöll, Christopher V. Synatschke

PMC · DOI: 10.1002/mabi.202500585 · Macromolecular Bioscience · 2026-01-23

## TL;DR

Researchers created nanofibers with growth factors that boost neuron growth, which could help in tissue regeneration.

## Contribution

Novel hybrid nanofibers combining growth factors with self-assembling peptides were developed to enhance neuronal growth.

## Key findings

- FGF2-SAP and IGF1-SAP nanofibers stimulated mouse neuron growth better than individual growth factors or SAPs alone.
- Combinations of FGF2-SAP and IGF1-SAP nanofibers increased neuron survival compared to single GF-SAP treatments.
- The hybrid nanofibers stably present multiple growth factors, offering potential for in vivo tissue regeneration.

## Abstract

Growth factors (GF) fulfil essential functions during organ development and regeneration. In tissue regeneration, evidence suggests that the combined application of several GFs is more efficient compared to their individual application. Single or multiple GFs are often applied to animal models of organ regeneration through release by hydrogels. Such hydrogels are often formed by self‐assembling peptides (SAPs) spontaneously polymerizing into peptide nanofiber (PNF) networks. In this study, we established PNFs by conjugating an SAP backbone (KIKIQIN) with bioactive peptide sequences derived from two GFs, FGF2 and IGF1. This resulted in the GF‐mimicking fusion peptides FGF2‐SAP and IGF1‐SAP, respectively. In these PNFs, both GFs were stably incorporated rather than released as in the case of PNF‐derived hydrogels. When individually added to culture medium, FGF1‐SAP and IGF1‐SAP stimulated the growth of mouse primary hippocampal neurons. Notably, their growth‐stimulating potential exceeded neuronal growth achieved with the SAP backbone or the GF peptides alone. Finally, combinations of FGF2‐SAP, IGF1‐SAP, and the SAP backbone were tested, which formed FGF2 and IGF1 presenting PNFs. Indeed, specific GF‐SAP combinations resulted in elevated numbers of surviving neurons compared to individual application. In summary, in this study, we identified novel GF‐SAP hybrid nanofibers capable of stimulating cellular growth. Such nanofibers, enabling stable and simultaneous presentation of multiple GFs, might be well suited for tissue regeneration in vivo.

In this study, novel hybrid nanofibers composed of self‐assembling peptides (SAPs) conjugated with peptides derived from two growth factors (GFs), FGF2 and IGF1, were produced (FGF2‐SAP and IGF1‐SAP). Those hybrid nanofibers stimulated cellular growth of primary mouse neurons. In addition, nanofibers simultaneously presenting both GFs also enhanced neuronal growth. Such nanofibers might be well suited for tissue regeneration in vivo.

## Linked entities

- **Proteins:** FGF2 (fibroblast growth factor 2), IGF1 (insulin like growth factor 1)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Sh2d1a (SH2 domain containing 1A) [NCBI Gene 20400] {aka Gm686, SAP}, Fgf2 (fibroblast growth factor 2) [NCBI Gene 14173] {aka Fgf-2, Fgf2a, Fgfb, bFGF}, Fgf1 (fibroblast growth factor 1) [NCBI Gene 14164] {aka Dffrx, Fam, Fgf-1, Fgf2b, Fgfa}, Ngf (nerve growth factor) [NCBI Gene 18049] {aka Ngfb, beta-NGF}, Tubb3 (tubulin, beta 3 class III) [NCBI Gene 22152] {aka 3200002H15Rik, M(beta)3, M(beta)6}, Stag2 (STAG2 cohesin complex component) [NCBI Gene 20843] {aka 9230105L23Rik, B230112I07Rik, SA-2, SAP2}, Pphln1 (periphilin 1) [NCBI Gene 223828] {aka CR, HSPC206, HSPC232}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], FGFR1 (fibroblast growth factor receptor 1) [NCBI Gene 2260] {aka BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, Skap2 (src family associated phosphoprotein 2) [NCBI Gene 54353] {aka 2610021A10Rik, RA70, SKAP-HOM, Saps, Scap2, mSKAP55R}, Lsamp (limbic system-associated membrane protein) [NCBI Gene 268890] {aka 5430428I19, B130007O04Rik, D930023J12Rik, Gm29907, Lam, Lamp}, Ptprh (protein tyrosine phosphatase receptor type H) [NCBI Gene 545902] {aka R-PTP-H, sap-1}, Igf1 (insulin-like growth factor 1) [NCBI Gene 16000] {aka C730016P09Rik, Igf-1, Igf-I}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, Gm2a (GM2 ganglioside activator protein) [NCBI Gene 14667] {aka GM2-AP, SAP-3}
- **Diseases:** PNF (MESH:C565529), traumatic brain injury (MESH:D000070642), nerve or skin injury (MESH:D000080902), DIC (MESH:C536108), amyloid (MESH:C000718787), spinal cord injury (MESH:D013119), ischemia (MESH:D007511)
- **Chemicals:** magnesium chloride (MESH:D015636), acetonitrile (MESH:C032159), DMF (MESH:D004126), CHCA (-), ACN (MESH:C084683), Phalloidin (MESH:D010590), alpha-cyano-4-hydroxycinnamic acid (MESH:C007175), Peptides (MESH:D010455), Congo Red (MESH:D003224), Diethyl ether (MESH:D004986), TFA (MESH:D014269), heparin (MESH:D006493), Alexa Fluor 488 (MESH:C000711379), imidazole (MESH:C029899), DIC (MESH:C081611), amino acid (MESH:D000596), DAPI (MESH:C007293), glucose (MESH:D005947), CO2 (MESH:D002245), DIPEA (MESH:C027070), PBS (MESH:D007854), water (MESH:D014867), KCl (MESH:D011189), His (MESH:D006639), hydrogen (MESH:D006859), fluorescamine (MESH:D005450), Piperidine (MESH:C032727), calcium chloride (MESH:D002122), DMSO (MESH:D004121), EDTA (MESH:D004492), carbon (MESH:D002244), DCM (MESH:D008752), Triton-X-100 (MESH:D017830), amine (MESH:D000588), ThT (MESH:C009462), uranyl acetate (MESH:C005460), copper (MESH:D003300), sucrose (MESH:D013395), Resin (MESH:D012116), Lys (MESH:D008239), DPBS (MESH:C012939)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rodentia (rodent, order) [taxon 9989], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12829522/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829522/full.md

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Source: https://tomesphere.com/paper/PMC12829522