As the most abundant component in extracellular matrices (ECM), collagen is widely used as the scaffold material in tissue engineering (Wang Y. et al., 2023). Collagen contains arginine-glycine-aspartic acid (RGD)-motifs, which capable of mediate cell adhesion (Wu et al., 2021). Collagen is not only the main component of dental pulp and periodontium, but also the biomineralization matrix of dentin and bone. Thus, collagen-based bioink have been used for the reconstruction of dental pulp, periodontal ligament, and alveolar bone (Duarte Campos et al., 2020; Lee U.-L. et al., 2021; Li et al., 2022). Despite good biocompatibility, flexibility, and low immunogenicity, the poor mechanical property limit collagen’s use as bioinks. Incorporation with other hydrogel or organic/inorganic materials may be a feasible approach to improve mechanical stability and broaden the application boundaries of collagen-based bioink (Lee J. M. et al., 2021).

Derived from exoskeletons and shells of crustaceans, chitosan is abundant in nature and known as a widely used scaffold material in tissue engineering. Chitosan possesses high biocompatibility, hydrophilicity, and controllable biodegradability (Szulc and Lewandowska, 2022). Moreover, a broad spectrum of antibacterial properties makes it unique advantage for the dental application (Li Y. et al., 2020). Numerous studies have proven that 3D-printed chitosan-based scaffold can be employed for dental tissue regeneration due to its tunable physiochemical properties and favorable biological response (Suo et al., 2023). EzEldeen et al. (2021) explored the effects of chitosan source (animal vs. fungal), co-polymerization with gelatine, and crosslinking agent (3-glycidyloxyproply trimethoxysilane, GPTMS or genipin) on scaffold properties and biological response. However, the low mechanical property and sterilization strict the application of chitosan-based hydrogel in the bioprinting field (Lazaridou et al., 2022). Therefore, many attempts have been made to enhance the mechanical strength of chitosan by functional groups modification and co-crosslinking with other molecules (Liu et al., 2021; Salar Amoli et al., 2022).

As a natural biopolymer, alginate attracted scientists’ focus for its water solubility and rapidly cross-linked by calcium ions at room temperature. Besides, alginate possesses proper mechanical property, tunable viscosity and acceptable printability, which make it suitable for bioprinting technique (Gao et al., 2021). However, the pure alginate lacks RGD motifs for cell attachment, and the enzyme that cleave alginate chain is absent in human body, leading to the uncontrollable biodegradation in vivo. Given that, alginate is often used with other materials to form composites for bioinks (Rastogi and Kandasubramanian, 2019; Yu et al., 2019).

Bioceramic materials, including β-tricalcium phosphate (β-TCP), hydroxyapatite (HA), bioglass, calcium silicate (CS) and so on, have been well investigated as scaffold materials in traditional tissue engineering manufacturing for their excellent biocompatibility, favorable bioactivity and easy tailored characters (Baino et al., 2015). Owing to the intrinsic similar to the inorganic composition of bone and tooth, bioceramics are often used for the regeneration of hard tissues. But they also have disadvantages of low fracture resistance, low flexural resistance and wettability (Raveau and Jordana, 2020).

Typically, bioceramics often added as fillers to the polymer matrix to obtain ideal physicochemical and mechanical properties. A study conducted by Ahlfeld et al. (2023) indicated that varieties of mineral fillers, including CaCO₃, SrCO₃, strontium-modified hydroxyapatite (SrHAp) or tricalcium phosphates, integrated into a PLGA matrix can remarkably modify the degradation behavior of printed scaffold and an increase of the specific alkaline phosphatase activity were observed. Besides, mesoporous calcium silicate is also used in hard tissue regeneration as a component of biomaterial inks because of its ability to sustained release Si ions and other bioactive agents (Huang et al., 2018; Yeh et al., 2022). A bioactive strontium-doped calcium silicate (SrCS) scaffold released Sr and Si ions even after 6 months and enhanced secretion of osteogenic-related proteins (Wang et al., 2021).

Commonly, hydrogels are mixed with bioceramics particles for enhanced mechanical stability and adjustable biological properties. Tian et al. explored a novel bioink composed of sodium alginate (SA), gelatin (Gel), and nano-hydroxyapatite (na-HA). The SA/Gel/na-HA hydrogel exhibited shear-thinning behavior, optimized equilibrium swelling rate and compression modulus, as well as significantly improved the osteogenic differentiation of human periodontal ligament stem cells (hDPLSCs) (Tian et al., 2021).

Gelatin methacryloyl (GelMA) is a gelatin derivative modified by methacrylamide and methacrylate groups. Resembling the native ECM, GelMA contains many RGD-sequences for cell attachment as well as matrix metalloproteinase (MMP)- degradable motifs for cell remolding (Yue et al., 2015). As a photo-crosslinked hydrogel, GelMA undergoes photoinitiated radical polymerization without chemical crosslinkers that may be detrimental to cells (Klotz et al., 2016). For its tunable mechanical characteristics and suitable biological properties, GelMA is a versatile matrix that can be vastly used in biomedical application (Sakr et al., 2022). Numerous studies have proven that GelMA-based scaffolds can promote cell viability and osteo/odontogenetic differentiation of dental stem cells, including DPSCs, PDLSCs and SCAPs (Ha et al., 2020; Buyuksungur et al., 2021; Zhu et al., 2023).

Not only served as cell delivery vehicles in bioprinting, GelMA also plays a key role in drug and growth factor delivery due to its biodegradable properties. Park et al. (2020) developed bone morphogenetic protein (BMP) peptide-tethering bioink by conjugating peptides to GelMA. The results showed that BMP-mimicking peptide remained in bioprinted construct for more than 50% after 3 weeks and robustly increased the expression of odontogenic-related genes of hDPSCs.

A study conducted by Choi et al. (2022) used two different types of MTA (ProRoot MTA and Endosem Zr) combined with GelMA and evaluated the biological effects on hDPSCs. Although 3D-printed MTA/GelMA scaffolds showed more calcium deposition, elevated expression of odontogenetic-related genes was not statistically significant. Lin et al. fabricated the composite scaffold with CS reinforced-GelMA bioink. The CS/GelMA bioink is capable of inducing odontogenic differentiation of hDPSCs. Another study showed that the addition of mesoporous bioactive glass nanoparticles significantly enhanced shape fidelity, surface roughness, and bioactivity (Mei et al., 2022).

Synthetic polymers are another kind of vastly used materials in tissue engineering. They have the advantages of adjustable physical and chemical properties, which makes it suitable candidates for the dental tissue regeneration.

Polylactic acid (PLA) and poly(L-lactic-co-glycolic) acid (PLGA) are well-established polymers for their biosecurity approved by Food and Drug Administration (FDA) and excellent manufacturing ability. Moreover, PLGA possesses tunable degradation rate by different the ratio of lactic acid to glycolic acid, which can be employed as carries of biomedical substance (Danhier et al., 2012). However, both PLA and PLGA undergo hydrolytic degradation and generates acid degradation products that may trigger local inflammation in vivo, thus confine their application (Ramot et al., 2016; Li et al., 2017). Polycaprolactone (PCL) is also conventional scaffold material routinely used in 3D-printing and has desired biocompatibility and biodegradability. Nevertheless, the lack of cell-anchoring site and hydrophobic surface lead to the low bioactivity of synthetic polymers (Place et al., 2009). Various attempts have been made for the optimization of biological properties, including surface modification, biomaterial coating, introduction of functional groups and so on (Bow et al., 2021; Feng et al., 2021; Park et al., 2021).

Given that these traditional polymers often require organic solvent for dissolving in 3D printing process and cause solvent residue in the final construct, in recent years, waterborne biodegradable polyurethane (wPU) have shown great potential as 3D-printing materials (Hung et al., 2016). However, very few studies are found about PU application in the dental tissue regeneration. A study published recently employed PU scaffolds coated with boric acid. The wPU/boric acid scaffold can trigger the osteogenic differentiation of DPSCs without significantly reducing cell viability and proliferation (Çelebi-Saltik et al., 2023).

dECM refers to the natural tissue with the removal of immunogenic cellular components while three-dimensional network of ECM and biological molecules were remained, including various proteins and polysaccharides. Compared with other hydrogels, dECM provides not only mechanical support and adhesion cites for cells, but also biological cues to impact cell behavior by cell-ECM interactions (Zhang et al., 2022).

Several studies have proven that dECM derived from dental tissue/cells hold the capacities of recruiting stem cells, promoting osteogenesis, and forming pulp-like tissue (Smith et al., 2012; Heng et al., 2016; Nowwarote et al., 2021; Tan et al., 2021). Due to the rising demand for biomimetic microenvironments of 3D printed constructs, dECM is gradually becoming a promising bioink material (Kim et al., 2022; Yang et al., 2023).

Treated dentin matrix (TDM), also termed as “demineralized dentin matrix” (DDM), is a kind of specific dECM that referred to dentin matrix after a certain degree of demineralization treatment. With exposed dentin tubules and collagen fibrils, TDM released abundant dentinogenetic-related biomolecules including COL-1, DSPP, DMP-1, TGF-β1, decorin, biglycan, and created an inductive microenvironment for dentin regeneration (Guo et al., 2009; Li et al., 2011). Athirasala et al. (2018) mixed the insoluble components of the DDM with alginate in 1:1 ratio, and then added extracted soluble dentin molecules, dramatically promoting hydrogel-encapsuled SCAPs differentiate into dentin. Besides, TDM particles are also used to form particle-based bioink and regenerate specific dental tissue or whole tooth (Huang et al., 2023).

Surrounded by rigid dentin walls, dental pulp is a loose connective tissue composed of cells (odontoblasts, fibroblasts, DPSCs), collagen, nerves and blood vessels. Retaining vital pulp is of great importance for tooth nutrient, repairment, and sensory, especially for immature permanent teeth. When dental pulp infected, root canal therapy (RCT) remains the first-option in clinical practice. However, tooth after RCT is faced with problems such as persistent inflammation, discoloration, and increased fragility (Ricketts, 2001). While pulp revascularisation presents a promising clinical approach, it fails to reconstruct functional pulp-like tissue and leads to unexpected calcification (Chen et al., 2012). Therefore, stem cell-based regenerative endodontic therapy has attracted the worldwide attention.

To achieve cellular pulp regeneration, it is essential to create a microenvironment conducive to stem cell proliferation and differentiation. Hydrogel proves to be a fitting candidate owing to its resemblance to the natural ECM. Various hydrogel have been evaluated for pulp bioprinting, encompassing fibrin, hyaluronic acid, GelMA and so on (Han et al., 2019; Nejad et al., 2021; Cunha et al., 2023).

Pulp vascularization is one of the key objectives as well as challenges in functional pulp regeneration. Several strategies have been utilized including the sacrificial material method and co-culture with endothelial cells (Athirasala et al., 2017). Duarte Campos et al. (2020) injected collagen based bioink into prepared root canal via a handheld bioprinter. The results of immunofluorescence showed successful vascularization in the root canal without the shrink of bioink. However, these strategies have yet to demonstrate their feasibility in vivo.

Remarkably, in a recently published work, Qian et al. successfully fabricated DPSC-loaded GelMA microspheres via a DLP printer. These cell-loaded microspheres have improved stemness and higher multi-directional differentiation potential, including angiogenic, neurogenic, and odontogenic differentiation. The regeneration of vascularized and neutralized pulp-like tissue was demonstrated by subcutaneous transplantation in nude mice and in situ experiment in swine (Qian et al., 2023).

Periodontal ligament (PDL) is a connective tissue that is mainly composed of collagen type I fibers and proteoglycans. Owing to the firm attachment between cementum and alveolar bone and specific oriented collagen fibers, it provides mechanical stability and attenuate the masticatory stress to protect tooth. Furthermore, PDL contains an abundance of blood vessels and nerve endings that provide nourishment to the cementum and alveolar bone. Utilizing mesenchymal stem cells present in the periodontium, repairment and remodeling of periodontal tissue are possible (Hurng et al., 2011). Hence, the PDL regeneration is an essential part of periodontal regeneration.

3D printing holds its intrinsic advantage to form highly-arranged collagen fibers because of the exist of micro-strands and precise control of cell position in the 3D network. It has been proven that compared with cell-seeding bulk collagen, the cell-laden collagen by bioprinting showed significantly more lang periodontal ligament-like soft tissue on the surface of titanium implants (Lee U.-L. et al., 2021).

To physically control the orientations of fiber bundles, so called “fiber-guiding scaffold,” has emerged and attracted increasing focus. Lin H.-H. et al. (2021) fabricated a collagen-based waveform microfibers and evaluated the microcrimped scaffold under shear load (6 dyne/cm²). Compared with straight microfibers, waveform microfibers exhibited enhanced cell spreading and adhesion, as well as upregulated expression of periostin (a key molecule for extracellular matrix assembly).

Kim and Park (2020) created microgroove patterns on the scaffold surfaces with different slice intervals. After 7 days culture, the μG-25 (25.40 µm intervals) showed the ability to organize aligned PDL cells while the μG-6 (6.35 µm intervals) leaded random organization. Similarly, Pilipchuk et al. (2016) employed 3D-printed scaffold combined with micropatterned film to achieve regeneration and integration of alveolar bone and PDL. Their conclusions support that optimized surface tomography induce specific orientations of PDL fibers in a more predictable manner.

Gingiva is another key component of oral soft tissue, which is essential for oral structural integrity and dental aesthetics. Although autogenous gingival grafts have been widely used to reverse gingival recession and augment periodontal soft tissue, the lack of donor tissue sources, the complexity of the surgical procedures, and the postoperative pain and numbness still hamper a good prognosis (Yang M. et al., 2019). Therefore, the tissue engineering strategy seems to be a new option for regenerative oral soft tissue augmentation. Tang along with his team developed a kind of bioink composed of alginate, gelatin and injectable platelet-rich fibrin (i-PRF), which can release various repair-related growth factors. In vivo experiments, 3D-printed constructs with 50% i-PRF showed more collagen formation and host tissue infiltration compared to the group without. In their latest study, they bioprinted acellular dermal matrix (ADM)-based hydrogel composite and performed in vivo implantation in beagles, demonstrating that GF-loaded ADM scaffolds significantly promote keratinised gingival regeneration (Yi et al., 2022; Liu et al., 2023).

Dental enamel is the hardest tissue in the human body, providing external protection for the tooth against masticatory forces. As a kind of non-vascular, acellular, highly mineralized hard tissue, enamel is composed of substituted hydroxyapatite and organic macromolecules (Nanci, 2013). Since the enamel organ disappears at the end of the tooth germ development, there are no enamel epithelial cells in a mature tooth, resulting in the lack of enamel regeneration ability. Thus, development of alternative approaches to repair and regenerate enamel defects is much needed but remains challenging due to the highly-ordered hydroxyapatite structure. Zhao et al. (2022) used supergravity preparation technology and hydrothermal treatment to disperse the Hap nanorods in the hybrid resin-based composites (RBCs), developing a new bioactive ink. The printed tooth crown possesses multi-scale highly ordered structure and strong mechanical strength. Mohabatpour et al. (2022) combined carboxymethylcellulose (CMC) and alginate to create a new bioink that induced the differentiation of dental epithelial cells (HAT-7) to enamel-forming cells and promoted Ca and P deposition as well as matrix mineralization in vitro.

Human dentin is composed of hydroxyapatite (70% by weight) and an organic matrix (35% by weight) of collagenous and noncollagenous proteins, such as dentin sialophosphoprotein (DSPP), dentin matrix protein-1 (DMP-1), osteopontin, and osteocalcin (Zhang et al., 2014). Dentin regeneration is one of the most explored parts in the field of dental tissue engineering. 3D printing is capable of forming customed macro structures and intricated interconnections. Compared with conventional cast-molded hydrogel, 3D-printed alginate/gelatin scaffold can better promote the cell adhesion, viability, and osteogenic/odontoblastic differentiation of hDPSCs (Yu et al., 2019). Besides, 3D printed Biodentine/PCL scaffold exhibited a good apatite-forming ability and induced hDPCs proliferation and differentiation (Ho et al., 2018).

Incorporation of biological cues also helps to induce the odontogenic differentiation of stem/progenitor cells, and then promote the secreting and mineralization of dentin matrix. The extracts of dentin matrix, both soluble and insoluble molecules, significantly enhanced odontogenic differentiation of SCAPs encapsulated in bioprinted hydrogels (Athirasala et al., 2018). Similarly, Han et al. (2021) mixed DDM particles with fibrinogen-gelatin to produce a DDM particle-based bio-ink, which enhanced the dentin-oriented differentiation of DPSCs. Besides, the study by Kim et al. indicated that supplemented with bone-derived dECM can accelerate the odontogenic differentiation of hDPSCs (Kim et al., 2022).

In addition to bioactive molecules, Yeh et al. (2022) fabricated a mesoporous calcium silicate/calcium sulfate (MSCS) scaffold and added quercetin, a novel bioactive molecule which can reduce inflammatory mediator and inhibit osteoclast activity, into the printed scaffold. The composite scaffold not only possessed better physicochemical and biological properties but also enhanced odontogenic and immuno-suppressive properties. Feng et al. (2021) coated a 5 nm thick titania layer via atomic layer deposition on the 3D printed PLA scaffold, and higher DPSCs plating efficiency and upregulated expression of osteocalcin compared with uncoated PLA scaffolds were observed.

Alveolar bone loss is often caused by periodontitis or peri-implant inflammation. Regeneration of alveolar bone is one of the goals of periodontal therapy, and it is also a prerequisite for implant restoration. Compared with other craniomaxillofacial bone constructs, alveolar bone scaffold design and manufacture as a tooth-supporting tissue remains a challenge due to the structural complexity and geometric adaptability of tooth-root surface.

Bioceramics play a crucial role in the bone tissue engineering. Qin et al. explored the effect of different pore dimensions (Ø 480, 600, and 720 μm) on mechanical properties, bioactive ion release, and bio-dissolution of bioceramic scaffolds. The 600 μm group exhibited maximal new bone formation in the rabbits’ mandibular bone defects model (Qin et al., 2022). In another study, Osteoink™, composed of hydroxyapatite and α-TCP, was utilized to develop calcium phosphate (CaP)-based bioceramic scaffolds for alveolar bone reconstruction. The printed scaffolds had a high degree of accuracy to fit the respective clinical defects for which they were designed (Anderson et al., 2022). A newly developed bioceramic material, ∼10% Mg-substituted wollastonite (Ca90%Mg10%SiO3; CSi-Mg10) was also used to fabricated customed scaffolds for reconstruction of alveolar bone defect, exhibited desired osteoconduction, osteoinductivity and adequate biodegradation (Shao et al., 2018).

GelMA is another well-established material for alveolar bone reconstruction by virtue of its analogue to extracellular matrix and adjustable physicochemical properties. 3D-printed PCL/GelMA hybrid scaffolds yielded cell viability, osteogenic differentiation of DPSCs and mineralization in vitro (Buyuksungur et al., 2021). Tang et al. (2022) combined HERS cells and dental papilla cells (DPCs) to mimic the micro-environment of cell-cell interaction. Plenty of mineralization texture were observed when transplanted into the rat’s alveolar sockets. GelMA/PEGDA hybrid hydrogel were fabricated by controlling the volume ratio of GelMA-to-PEGDA. The results indicated that the 4/1 GelMA/PEGDA composite hydrogel exhibited best performance in osteogenic differentiation and formed new bone tissue in vivo (Ma et al., 2017). Luo et al. (2022) developed GelMA/β-TCP hybrid scaffolds which showed good biocompatibility and mechanical properties, and stimulated osteogenesis of BMSCs.

Furthermore, the supplement of growth factors, peptides, and other bioactive substances undoubtedly endows 3D printed constructs with superior biological properties, such as antimicrobial peptide KSL-W (Li et al., 2022), recombinant human erythropoietin (rh-EPO) (Liu H. et al., 2022) and graphene oxide (Park et al., 2021).

The dentin and dental pulp derived from dental papilla, which is formed during tooth germ development and participate in tooth activities together as the dentin–pulp complex (Abbass et al., 2020). Dentin offers durable shielding for the pulp, whereas the pulp supplies essential nutrients for the dentin and generates tertiary dentin as a response to caries, mechanical injury, or acid erosion. Therefore, the regeneration of vital dentin-pulp complex is the ideal target for endodontic medical treatment.

It has been widely studied that the fate of stem cells is closely associated with ECM characteristics (Liu et al., 2018). In this regard, Han et al. (2019) developed hDPSCs loaded bioink with different fibrinogen content to print dentin and pulp tissues (F20 for dentin, F5 for dental pulp) respectively. Bilayer scaffolds with region-specific induced soft and hard tissues are likewise seen as one of the viable strategies. Nejad et al. (2021) constructed PCL/45S5 bioglass (BG)-PCL/hyaluronic acid (HyA) scaffold and evaluated the physicochemical properties of the hybrid scaffold. The results showed that PCL/BG scaffolds had superior mechanical strength and surface roughness, and the PCL/HyA scaffolds possessed increased hydrophilicity for cell adhesion. Recently, Cunha et al. (2023) utilized 3D-printed microgels doped with dentin matrix molecules for direct dental pulp capping. Although both the microgel group supplemented with DMM particles and the MTA group showed the formation of organized pulp tissue, dentin-like tissue and new blood vessels, the presence of DMM helped to promote dentin bridge formation and exhibited more tertiary dentin deposition and attenuate less pulp necrosis.

Periodontitis is one of the most prevalent oral diseases in the world, resulting in periodontal attachment loss, alveolar bone resorption, even tooth loss (Kwon et al., 2021). The goal of periodontal treatment is to control the infection and reconstruct the functional tooth-supporting tissue. Guided tissue regeneration (GTR) is currently gold standard of periodontal tissue reestablishment by a barrier membrane to allow selective repopulation of PDL cells and bone, yet it still suffers from various limitations as well as clinical variability (Karring et al., 1993). The periodontal complex comprises multiple tissues, including periodontal ligament, cementum and alveolar bone, forming a “sandwich-like” structure. Herein, multiphasic scaffolds to mimic the cementum-PDL-alveolar bone complex has increasingly attracted the attention of researchers (Ivanovski et al., 2014).

In previous studies, Lee CH and his colleagues developed various growth factor-releasing scaffolds by loaded PLGA microspheres for periodontal tissue regeneration. They initially achieved integrated cementum-like tissue on the surface of dentin with high expression of cementum matrix protein 1 (CEMP1), an important marker of cementogenesis (Cho et al., 2016). Their another study used multiphase scaffolds for periodontium complex regeneration via spatiotemporal delivery of multiple bioactive cues, involving recombinant human amelogenin, CTGF and BMP-2. They also demonstrated the different microstrands spacing have an effect on the generation of integrated multiple tissues (Lee et al., 2014). Consistent with Lee’s studies, Daghrery et al. engineered PCL scaffold with F/Ca coating and revealed that aligned fibers strongly support ligamentogenesis and scaffold architecture with 500 μm strands spacing supports osteogenesis. The results of Masson’s trichrome staining indicated that the tissue-specific scaffold induced the regeneration of both soft and hard tissue in vivo (Daghrery et al., 2021; Daghrery et al., 2023). Furthermore, a novel composite hydrogel was designed as cell-laden bio-ink, encapsulating BMP-2 and PDGF that effectively facilitate alveolar bone regeneration and promote gingival healing respectively in the periodontal defect model of beagles (Miao et al., 2023). Ma et al. (2023) reported biomimetic periodontium patches (BPPs) by DLP technology. The BPPs featuring correctly oriented fibers and the assessment of clinically functional properties proved the regenerative periodontium can stand orthodontic migration force to achieve stable tooth movement.

Another important challenge to be solved is the interface integration. Soft-to-hard tissue interfaces have always been a tricky problem in tissue engineering for the difficulty to reproduce interface enthesis (Calejo et al., 2019). To overcome the lack of adhesion between newly formed PDL and bone, Blaudez et al. (2023) designed a decellularized construct consisting of consisting of PDL cell sheet and PCL scaffold for tissue-specific periodontal regeneration. Before decellularization, the biphasic construct was cultured for 24 h to allow cell sheet adhesion and enhance the cohesion between periodontium and bone part. Yao et al. (2022) introduced a transition region with 500-µm filament spacing, while the bone region was 250-μm filament spacing and the PDL region was consisted of aligned PCL filaments. The transition region separated the tissue-specific regeneration in the other two parts at the early time and promoted cellular cross-communication later between two regions. The insertion of ligamentous fibers towards the bone and calcium gradient were observed in the transition space. Similarly, Golafshan et al. (2023) fabricated a tri-layer scaffold in which PCL matrix with MgP was for bone, highly aligned PCL fibers were presented for PDL and random PCL fibers were printed to mimic the bone-to-PDL interface. The tri-layer scaffold showed enhanced mechanical stability and achieved coordinated periodontal tissue regeneration in the rodent model. Moreover, a recent study reported a biomimetic periodontal module with high architectural integrity. The module provided high-precision topographical cues and biochemical environment conducive to regulating cell behavior and achieving periodontal regeneration with the enthesis of the bone-ligament interface and well-aligned fibers in a beagle model (Yang et al., 2023).

Whole tooth regeneration with natural tooth morphology and function is the ultimate goal of dental regenerative medicine. Back in 2010, Kim et al. fabricated anatomically shaped human molar scaffolds and rat mandibular incisor scaffolds by 3D printing and performed orthotopic implantation of rat incisor scaffolds, combined with the delivery of SDF1 and BMP7. After 9 weeks, the histological results revealed regeneration of the PDL-like tissue and new bone at the interface between the scaffolds and native alveolar bone (Kim et al., 2010). While it is possible to replicate the morphology of natural teeth, grafts often struggle to form a strong enough periodontal bond with the host jawbone in a short period of time, which can compromise their ability to withstand substantial occlusal forces.

Tooth germ recombination appears to be another viable path to achieving whole tooth regeneration (Zhang and Yelick, 2021). Studies have been conducted to generate bioengineered tooth germs by the reconstruction of dental epithelial and mesenchymal cells (Ono et al., 2017). However, it is still tough to regenerate eruption-competent tooth germs hence the epithelial-mesenchymal transition during tooth development is yet to be completely unveiled and replicating spatiotemporal interactions between different cells remains challenging. 3D bioprinting technology is thought to offer new possibilities for bioengineered tooth germ due to its ability to precisely control microstructures at the cellular level.

Therefore, fabricating bioengineered roots, also known as “bio-root,” and then restoring with artificial crown seem to be a much more feasible approach. Bio-root, referred to the bioengineered tooth root, was firstly proposed by Sonoyama in 2006 and has demonstrated the ability to regenerate dentinal tubule-like and periodontal ligament-like structures in swine model (Wei et al., 2013). Up to recently, Huang et al. developed a personalized 3D-printed scaffold with PCL and TDM. Notably, the TDM scaffolds combined with DFSC sheets served as an analogue to natural tooth root and with satisfied angiogenic capacity in orthotopic transplantation in beagles (Huang et al., 2023).

Besides, a study by Chen et al. fabricated personalized bio-root by DLP printing of hydroxyapatite bioceramic. Bioceramic sintered at 1,250°C exhibited almost twice elastic modulus than natural decellularized dentine, which significantly enhanced the physicochemical properties of Hap. The nano-HAw (nano-hydroxyapatite whiskers) coating improved both mechanical property and surface hydrophilicity, and periodontal ligament-like enthesis formation in-situ transplantation in rat alveolar fossa (Chen et al., 2023).