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Salivary glands are the principal organs responsible for secreting saliva in the oral cavity. Tumors, trauma, inflammation, and other factors can cause functional or structural damage to the glands, leading to reduced saliva secretion. In this study, we innovatively prepared a acinar-mimetic silk fibroin-collagen-astragalus polysaccharide (SCA) scaffold using low-temperature three-dimensional (3D) printing and freeze-drying techniques. We evaluated the material properties and cell compatibility of the scaffold in vitro and implanted it into the damaged parotid glands (PG) of rats to assess its efficacy in tissue reconstruction and functional repair. The results demonstrated that the SCA scaffold featured a porous structure resembling natural acini, providing an environment conducive to cell growth and orderly aggregation. It exhibited excellent porosity, water absorption, mechanical properties, and biocompatibility, fulfilling the requirements for tissue engineering scaffolds. In vitro , the scaffold facilitated adhesion, proliferation, orderly polarization, and spherical aggregation of PG cells. In vivo , the SCA scaffold effectively recruited GECs locally, forming gland-like acinar structures that matured gradually, promoting the regeneration of damaged PGs. The SCA scaffold developed in this study supports tissue reconstruction and functional repair of damaged PGs, making it a promising implant material for salivary gland regeneration. [ABSTRACT FROM AUTHOR]

• A high accuracy deformation measurement method for semi-continuous materials is proposed. • The deformation field of 3D printed scaffolds is accurately measured. • The first visualization of cell differentiation on scaffolds was achieved by experimental measurements. • The effects of loading in vitro and water content on cell differentiation were investigated. • This work corroborates that in vitro loading culture and modulation of scaffold pore structure can be exploited to design scaffolds with regions that guide specific tissue development. Three-dimensional (3D) mechanical microenvironments, such as 3D strain fields in tissue engineering scaffolds have a crucial impact on the interactions between scaffold architecture, mechanical stimuli, and tissue differentiation. However, the discontinuity induced by the pores poses a challenge to the measurement of the 3D strains of the scaffolds. Herein, we present a tissue engineering scaffold optical coherence elastography (TES-OCE) method to visualize the full-field 3D strain fields of the tissue engineering scaffolds when cells are cultured on them and to explore the relationship between mechanical stimulation and cell differentiation. A semi-continuous digital volume correlation (SC-DVC) method based on a material component identification algorithm was proposed to automatically extract the scaffold architecture information and obtain the 3D strain fields with high accuracy. The non-uniform deformation field of a 3D printed tissue engineering scaffold with various water contents under loading in vitro was measured by the TES-OCE method, based on the tissue shear strain field obtained above, the area of cell differentiation phenotype on tissue engineering scaffolds was accurately predicted. Experimental results show that the loads and water absorption of the scaffold significantly affects the 3D tissue shear strain field in the tissue engineering scaffold. Thus, the cell differentiation fate can be modulated by loading culture and scaffold pore structure. The TES-OCE provides a new experimental method to delineate the interrelationship between tissue engineering scaffolds, the mechanical microenvironment, and cell proliferation and differentiation. It may be further developed as an effective tool to guide the design and development of superior tissue engineering scaffolds. [ABSTRACT FROM AUTHOR]

A biomaterial that can remove remaining oral squamous cell carcinoma (OSCC) cells and repair oral mucosal damage is urgently needed. This graphical abstract described a composite scaffold that would simultaneously kill OSCC cells and promote the regeneration of the oral mucosa. [Display omitted] • Quercetin acts as an inhibitor when heat shock proteins make tumor cells more resistant to photothermal therapy. • Ti 3 C 2 MXene and quercetin are effectively carried by scaffold made of collagen and silk fibroin. • The composite scaffold successfully limits tumor cells migration and promotes oral mucosal defects regeneration. The most prevalent oral and maxillofacial cancer is oral squamous cell carcinoma (OSCC). Patient survival is compromised by relapse due to post-operative tumor remnants and significant mucosal defects. Photothermal therapy (PTT) is used to ablate local malignancies, but the capacity of tumor cells to resist it is correlated with the overexpression of heat shock protein 70 (HSP70). In this work, PTT and tissue engineering scaffold were rationally integrated to construct a Ti 3 C 2 MXene, collagen, silk fibroin and quercetin composite scaffold (M-CSQ scaffold), a 3D printed biomaterial that simultaneously kill OSCC cells and promote the regeneration of the mucosal defects. The M-CSQ scaffolds were prepared by cryogenic 3D printing and freeze-drying techniques with sufficient pores that allow an abundant cell migration and provide a proliferation space. Ti 3 C 2 MXene has excellent photothermal conversion ability and stability. Quercetin targeted HSP70 to decrease its expression in OSCC cells, consequently weakening their resistance to high temperature and enhancing the effect of PTT. The M-CSQ scaffold effectively killed OSCC cells in vitro and inhibited tumor growth in vivo. In addition, the M-CSQ scaffold provided adhesion sites for Sprague-Dawley rat (SD rat) buccal mucosal fibroblasts and promoted the repair of buccal mucosal wounds. [ABSTRACT FROM AUTHOR]