# The influence of different surface texture parameters on the cell proliferation and adhesion early behaviors on the surface of titanium alloy

**Authors:** Fuqiang Lai, Changsheng Cao, Linfeng Xie, Mingxuan Shang, Wenge Liu, Yumei Li, Zhihuang Qiu, Liangwan Chen

PMC · DOI: 10.3389/fbioe.2026.1679515 · 2026-02-03

## TL;DR

This study shows how laser-processed titanium surfaces with specific textures can improve cell adhesion and growth, which is important for heart devices like LVADs.

## Contribution

The study introduces a method using femtosecond laser processing to optimize titanium alloy surfaces for better biocompatibility in medical devices.

## Key findings

- Surface texturing significantly enhances cardiac fibroblast adhesion and modifies growth patterns on titanium substrates.
- A texture depth of 20 μm was found to be optimal for cellular proliferation and adhesion.
- Square patterns showed the strongest pro-proliferative effects among tested geometries.

## Abstract

Current clinical practice has extensively validated the efficacy of left ventricular assist devices (LVADs) in managing end-stage heart failure. A persistent challenge across all ventricular assist systems involves achieving optimal biocompatibility at the critical interface between the LVAD outlet and myocardial tissue. In this study, femtosecond laser processing (FLP) technology was utilized to engineer microtextured surfaces with controlled geometric parameters on the titanium alloy surface. The experimental design systematically assessed surface morphology and compositional variations for four distinct patterns (circular, triangular, square, hexagonal) and three texture depths (10, 20, 40 μm). FLP demonstrated favourable microstructural fabrication quality, producing defined pattern boundaries with minimal thermal impact on adjacent regions. While all textured surfaces exhibited characteristic periodic processing marks at their bases, increased texture depth correlated with progressive roughness amplification in these basal regions. Elemental analysis revealed that oxygen enrichment specifically along texture peripheries compared to untextured surfaces. Cellular early response studies demonstrated that surface texturing significantly enhanced cardiac fibroblasts adhesion on titanium substrates while concurrently modifying fibroblast growth patterns. Quantitative analysis identified 20 μm as the optimal texture depth for cellular proliferation and adhesion, outperforming both shallower (10 μm) and deeper (40 μm) configurations. Geometric comparisons indicated that square patterns induced the best pronounced pro-proliferative effects, followed by hexagonal patterns. Mechanistic observations suggest that surface micro-roughness facilitates initial cell adhesion, with subsequent proliferation biodynamics being governed by topographical guidance effects. These findings establish clear structure-function relationships between engineered surface parameters and biological responses, providing significant insights for LVAD surface treatment and optimization.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** Ptk2 (PTK2 protein tyrosine kinase 2) [NCBI Gene 14083] {aka FADK 1, FAK, FRNK, Fadk, p125FAK}, ACTE1 (actin epsilon 1) [NCBI Gene 528168], ALB (albumin) [NCBI Gene 280717]
- **Diseases:** osteosarcoma (MESH:D012516), infection (MESH:D007239), end-stage heart failure (MESH:D007676), cytotoxicity (MESH:D064420), thrombotic (MESH:D013927), heart failure (MESH:D006333), thromboembolic complications (MESH:D013923), RCF (MESH:D006331)
- **Chemicals:** Ni (MESH:D009532), FITC (MESH:D016650), N (MESH:D009584), EDTA (MESH:D004492), Triton X-100 (MESH:D017830), polymers (MESH:D011108), carbon (MESH:D002244), O (MESH:D010100), diamond- (MESH:D018130), gentamicin (MESH:D005839), ethanol (MESH:D000431), water (MESH:D014867), Fe (MESH:D007501), V (MESH:D014639), MTT (MESH:C070243), Ti (MESH:D014025), Ti-6Al-4V (MESH:C031462), Al (MESH:D000535), MEM medium (-), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), PBS (MESH:D007854), heparin (MESH:D006493), H (MESH:D006859), TiN (MESH:C041500), 4', 6-diamidino-2-phenylindole (MESH:C007293), DMSO (MESH:D004121), oxide (MESH:D010087), CO2 (MESH:D002245), TiO2 (MESH:C009495), paraformaldehyde (MESH:C003043)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Enterovirus C (no rank) [taxon 138950]
- **Cell lines:** L cell L-929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58), MG-63 — Homo sapiens (Human), Osteosarcoma, Cancer cell line (CVCL_0426), RCF — Homo sapiens (Human), Transformed cell line (CVCL_YJ37), fibroblasts — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594)

## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909512/full.md

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Source: https://tomesphere.com/paper/PMC12909512