# Nanoperlite Particles Enhance Fibrogenesis in Thyroid Orbital Fibroblasts: A Potential Activated Cell Source for Ocular Tissue Engineering

**Authors:** Fatemeh Sanie-Jahromi, Razi Sahraeian, Behzad Khademi

PMC · DOI: 10.1155/bmri/1795961 · BioMed Research International · 2026-03-08

## TL;DR

Nanoperlite particles at 1 μg/mL boost fibroblast activity in thyroid eye disease cells, offering potential for ocular tissue repair.

## Contribution

Demonstrates nanoperlite's concentration-dependent enhancement of fibrogenesis in thyroid orbital fibroblasts.

## Key findings

- Nanoperlite at 1 μg/mL significantly upregulated fibrogenesis-related genes in orbital fibroblasts.
- Higher nanoperlite concentration (10 μg/mL) did not show similar gene expression enhancement.
- Nanoperlite shows potential for ocular tissue engineering at specific low concentrations.

## Abstract

Fibroblasts are crucial in tissue engineering because of their ability to synthesize the extracellular matrix (ECM) and secrete growth factors. Orbital fibroblasts (OFs) from patients with thyroid eye disease (TED) exhibit enhanced fibroblastic properties, making them ideal candidates for regenerative medicine in ocular tissue. In the present study, we investigated the effect of nanoperlite on TED OFs. Nanoperlite, with its unique properties including high silica (SiO2) content, holds promise for enhancing fibroblast functions. Nanoperlite was prepared and characterized in terms of particle size and chemical composition. A sample of orbital adipose tissue was taken from a TED patient during orbital decompression surgery and OFs were expanded in vitro. The cells were then treated with nanoperlite at concentrations of 1 and 10 μg/mL for 24 h, and gene expression related to the fibrogenesis process was assessed using real‐time PCR. Nanoperlite at 1 μg/mL significantly increased the expression of TGF‐β, CD90, α‐SMA, ZEB1, β‐Catenin, and Snail genes in OFs. However, at 10 μg/mL, this effect was not observed. This study highlights nanoperlite′s potential to enhance fibroblast activity specifically at the concentration of 1 μg/mL. This effect can potentially aid tissue engineering strategy for periorbital tissue repair and eyelid reconstruction. However, further research is needed to fully elucidate its therapeutic potential and safety profile.

## Linked entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], THY1 (Thy-1 cell surface antigen) [NCBI Gene 7070], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58], ZEB1 (zinc finger E-box binding homeobox 1) [NCBI Gene 6935], ctnnb1.S (catenin beta 1 S homeolog) [NCBI Gene 380441], SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615]
- **Chemicals:** SiO2 (PubChem CID 24261)
- **Diseases:** thyroid eye disease (MONDO:0001509)

## Full-text entities

- **Genes:** PIK3CG (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma) [NCBI Gene 5294] {aka IMD97, PI3CG, PI3K, PI3Kgamma, PIK3, p110gamma}, PIK3R2 (phosphoinositide-3-kinase regulatory subunit 2) [NCBI Gene 5296] {aka MPPH, MPPH1, P85B, p85, p85-BETA, p85beta}, THY1 (Thy-1 cell surface antigen) [NCBI Gene 7070] {aka CD90, CDw90}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, SNAI1 (snail family transcriptional repressor 1) [NCBI Gene 6615] {aka SLUGH2, SNA, SNAH, SNAIL, SNAIL1, dJ710H13.1}, PIK3R3 (phosphoinositide-3-kinase regulatory subunit 3) [NCBI Gene 8503] {aka p55, p55-GAMMA, p55PIK}, PIK3CD (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta) [NCBI Gene 5293] {aka APDS, IMD14, IMD14A, IMD14B, P110DELTA, PI3K}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, ZEB1 (zinc finger E-box binding homeobox 1) [NCBI Gene 6935] {aka AREB6, BZP, DELTAEF1, FECD6, NIL2A, PPCD3}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}
- **Diseases:** eyelid injuries (MESH:D005141), cytotoxicity (MESH:D064420), TED (MESH:D049970), vision impairment (MESH:D014786), fibrosis (MESH:D005355), wounds (MESH:D014947), optic nerve damage (MESH:D020221), inflammation (MESH:D007249)
- **Chemicals:** hyaluronic acid (MESH:D006820), K2O (MESH:C068440), PBS (MESH:D007854), Perlite (MESH:C003076), Al2O3 (MESH:D000537), iron (MESH:D007501), CO2 (MESH:D002245), water (MESH:D014867), streptomycin (MESH:D013307), polymer (MESH:D011108), nitrogen (MESH:D009584), zinc (MESH:D015032), penicillin (MESH:D010406), SiO2 (MESH:D012822), P (MESH:D010758), Si (MESH:D012825), DMEM (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** fibroblasts — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594), TED — Epinephelus awoara (Yellow grouper), Spontaneously immortalized cell line (CVCL_S930)

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968326/full.md

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Source: https://tomesphere.com/paper/PMC12968326