# Step‐Ladder Bioprinting to Align Collagen Fibers for Anisotropic Tissue Fabrication

**Authors:** Ilayda Namli, Yogendra Pratap Singh, Deepak Gupta, Syed Hasan Askari Rizvi, Yasar Ozer Yilmaz, Joao Vitor Silva Robazzi, Medine Dogan Sarikaya, Mehmet Baykara, Ibrahim T. Ozbolat

PMC · DOI: 10.1002/smll.202510498 · Small (Weinheim an Der Bergstrasse, Germany) · 2026-01-08

## TL;DR

A new bioprinting method aligns collagen fibers to create tissues with better structure and function, such as corneas and cartilage.

## Contribution

A novel step-ladder printing approach that enhances collagen fiber alignment and cellular guidance in 3D bioprinting.

## Key findings

- SLP 3D-printed constructs showed improved collagen fiber anisotropy and narrower angle distributions.
- SLP guided seeded cells to align with collagen fibers, enhancing tissue organization.
- Corneal and cartilage constructs demonstrated high transparency, shape fidelity, and native-like mechanical properties.

## Abstract

Aligned collagen microstructure is essential for the mechanical and biological function of anisotropic tissues. However, conventional engineering methods often fail to achieve consistent and tunable fiber alignment within complex geometries. In this study, we developed a step‐ladder printing (SLP) approach by incorporating successive segments of channels of variable widths into a custom barrel design, combining controlled extensional flows with 3D bioprinting to enhance collagen fiber alignment. The results revealed that constructs 3D‐printed via SLP demonstrated improved anisotropy of collagen fibers and narrower fiber angle distributions compared to both extrusion‐based bioprinting with a conventional straight nozzle and drop casting methods. Furthermore, SLP effectively guided the directionality of seeded cells, aligning them consistently with underlying collagen fibers. To exemplify the utility of SLP, we built corneal constructs, achieving high transparency and shape fidelity, and articular cartilage constructs, showing mechanical properties within the range of native tissue and supported extracellular matrix production. These results suggest that the SLP approach offers a strategy for fabricating complex anisotropic tissues with integrated fiber alignment and cellular guidance.

The step‐ladder printing platform includes successive segments of channels with varying widths in a custom barrel design. This design allows for improved anisotropy of collagen fibers during extrusion. To demonstrate its effectiveness, corneal constructs with high transparency and shape fidelity, as well as articular cartilage constructs, displaying mechanical properties within the range of native tissue and supported extracellular matrix production, were successfully shown.

## Full-text entities

- **Genes:** FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, ACAN (aggrecan) [NCBI Gene 176] {aka AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK}, ALCAM (activated leukocyte cell adhesion molecule) [NCBI Gene 214] {aka CD166, MEMD}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, EPCAM (epithelial cell adhesion molecule) [NCBI Gene 4072] {aka Ber-Ep4, BerEp4, DIAR5, EGP-2, EGP314, EGP40}, SYTL1 (synaptotagmin like 1) [NCBI Gene 84958] {aka JFC1, SLP1}
- **Diseases:** corneal injury (MESH:D065306), breast cancer (MESH:D001943), cancer metastasis (MESH:D009369), fatigue (MESH:D005221)
- **Chemicals:** Hoechst 33342 (MESH:C017807), 1,9-dimethylmethylene blue (MESH:C016401), Riboflavin (MESH:D012256), Fast Green (MESH:C035906), H&amp;E (MESH:D006371), Safranin O (MESH:C009195), Masson's Trichrome (-), silicon (MESH:D012825), Alexa Fluor 647 (MESH:C569686), Hematoxylin (MESH:D006416), hydroxyproline (MESH:D006909), Nuclear Fast Red (MESH:C523186), penicillin (MESH:D010406), EthD-1 (MESH:C018533), GAG (MESH:D006025), PBS (MESH:D007854), eosin (MESH:D004801), glutaraldehyde (MESH:D005976), sodium acetate (MESH:D019346), 4',6-diamidino-2-phenylindole (MESH:C007293), CO2 (MESH:D002245), sucrose (MESH:D013395), cysteine (MESH:D003545), paraformaldehyde (MESH:C003043), EDTA (MESH:D004492), FITC (MESH:D016650), xylene (MESH:D014992), streptomycin (MESH:D013307), Triton X-100 (MESH:D017830), chondroitin sulfate (MESH:D002809), Calcein-AM (MESH:C085925), OCT (MESH:C051883), phalloidin (MESH:D010590), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (MESH:C410687), HCl (MESH:D006851), Acetic acid (MESH:D019342), ascorbic acid (MESH:D001205), silicone (MESH:D012828), Alcian Blue (MESH:D000423), NaOH (MESH:D012972), ethanol (MESH:D000431), xanthan gum (MESH:C002563), Fast Red (MESH:C005215), water (MESH:D014867), iridium (MESH:D007495)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** A 23G, C for 20-30, S1500A
- **Cell lines:** MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062), HT15-1KT — Mus musculus (Mouse), Hybridoma (CVCL_A3CL)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12954373/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954373/full.md

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Source: https://tomesphere.com/paper/PMC12954373