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Developing Bioinspired Multi-Functional Tendon-Mimetic Hydrogels for Tissue Engineering


Design and processing of tendon-mimetic anisotropic composite hydrogels (ACHs). (A) Chemical structures of ANF and PVA and their intermolecular hydrogen bonding. (B) Schematics of the processing steps for ACH involving stretching and confined drying for the orientation of nanofiber assembly. (C) SEM images of isotropic ANF-PVA hydrogel (top) and ACH-80 (bottom). Scale bars, 1 μm. (D) Schematics of the multifunctional tendon-mimetic ACHs. Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973
Design and processing of tendon-mimetic anisotropic composite hydrogels (ACHs). (A) Chemical structures of ANF and PVA and their intermolecular hydrogen bonding. (B) Schematics of the processing steps for ACH involving stretching and confined drying for the orientation of nanofiber assembly. (C) SEM images of isotropic ANF-PVA hydrogel (top) and ACH-80 (bottom). Scale bars, 1 μm. (D) Schematics of the multifunctional tendon-mimetic ACHs. Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973

A research team from Hong Kong, China, has developed a new approach to creating biomimetic materials that emulate the architecture of natural biological tissues. In a report published in Science Advances, the team, comprising experts in physics, mechanical engineering, and electrical and electronic engineering, described the development of multifunctional tendon-mimetic hydrogels, which offer a high elastic modulus, strength, and fracture toughness. These materials are bioinspired by natural tendons and are designed to provide biophysical cues that mimic the interactions between collagen fibers and proteoglycans in tendons. The team has biofunctionalized the surface of these materials with bioactive molecules to present biophysical cues that impart behavioral similarities to those of cell attachment. Additionally, they have integrated soft bioelectronic components onto the hydrogels to facilitate a range of physiological benefits.


Materials engineering a biomimetic tendon


Materials scientists have been working for years to develop advanced biological materials for medical devices and tissue engineering platforms that emulate natural biological tissue architectures via materials engineering. However, the natural tissue architecture has a variety of characteristics that are difficult to synthetically replicate. The architecture of tendons, in particular, relies on the load-bearing capacities of the musculoskeletal system to provide biophysical cues that translate into cellular behaviors via interfacial interactions. In the past decade, researchers have devoted extensive research efforts to engineer tendon-mimetic materials with high structural anisotropy.


Creating an advanced polymer material in the lab


The research team developed anisotropic composite hydrogels by stretching and confining the material consisting of stiff and flexible polymer constituents. The resulting material demonstrated branched microstructures that mimicked collagen-like building blocks. They conducted extensive hydrogen bonding between the two polymer constituents to create a three-dimensional network with high toughness, where the fibrillar network did not undergo structural disintegration even under high levels of strain, leading to their consistent alignment. They then observed the characteristic fibrillar network of isotropic hydrogels that resembled hierarchical structures as seen in natural tendons—such efforts weren't as feasible with pre-existing synthetic hydrogels.

Mechanics of ACHs. (A and B) Tensile stress-strain curves of ACHs in the directions parallel (A) and perpendicular (B) to the fiber orientation, respectively, as compared with the responses of isotropic ANF-PVA hydrogels. The sample denoted as ACH-x corresponds to x% of imposed elongation during the prestretching-drying process. (C) Stiffness anisotropy of ACHs, as characterized by the ratio between initial tensile moduli parallel (Ep) and perpendicular/normal (En) to the fiber alignment. (D) Moduli and strengths of ACH-80 and ACH-60 as compared with those of natural tendons, ligaments, and other anisotropic hydrogels with tendon-mimetic characteristics. (E) Fracture energies of ACHs measured in the directions parallel and perpendicular to the fiber alignment, as compared with those of isotropic ANF-PVA hydrogels. (F) Cyclic tensile tests on ACH-80 in the direction parallel to the fiber alignment, with 7.5% of maximum imposed strain. Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973
Mechanics of ACHs. (A and B) Tensile stress-strain curves of ACHs in the directions parallel (A) and perpendicular (B) to the fiber orientation, respectively, as compared with the responses of isotropic ANF-PVA hydrogels. The sample denoted as ACH-x corresponds to x% of imposed elongation during the prestretching-drying process. (C) Stiffness anisotropy of ACHs, as characterized by the ratio between initial tensile moduli parallel (Ep) and perpendicular/normal (En) to the fiber alignment. (D) Moduli and strengths of ACH-80 and ACH-60 as compared with those of natural tendons, ligaments, and other anisotropic hydrogels with tendon-mimetic characteristics. (E) Fracture energies of ACHs measured in the directions parallel and perpendicular to the fiber alignment, as compared with those of isotropic ANF-PVA hydrogels. (F) Cyclic tensile tests on ACH-80 in the direction parallel to the fiber alignment, with 7.5% of maximum imposed strain. Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973

Biofunctionalization of the advanced polymers


The scientists next studied the structural characterization of the new polymer and its influence on cell behavior via interfacial interactions. They adopted chemical functionalization to present a cell adhesion motif such as the arginylglycylaspartic acid motifs to bind with integrins on the cell membrane. The researchers noted the successful biofunctionalization of the advanced materials by observing the adhesion of fibroblast cells on the material surfaces, while samples without surface functionalization did not demonstrate similar cell attachment. The Rho-associated protein kinase (ROCK) molecules played a significant role by regulating the contractile machinery of cells during cell morphological responses to surface topography and substrate mechanics. The material constructs additionally regulated the macrophage cell differentiation between the pro-inflammatory M1 variants and the pro-healing M2 variants to establish bio-favorable implantable devices.


Advanced materials applications as bioelectronics


The research team ultimately demonstrated multimodal physiological sensing by integrating the advanced materials into soft bioelectronics. Among these iterations, they adopted a serpentine design to create wafer-based electronics with high stretchability to withstand the prewashing-drying process of the materials. They used finite element analysis to assess stress distribution across the device and enhanced the stretchability of the electronic component by modifying its geometrical design for improved mechanical integrity.


Outlook

Mingze Sun and colleagues have engineered tendon-mimetic hydrogels with outstanding mechanics and functionality that predominantly originated from the assembly of nanofibers. They used biophysical cues presented by the materials constituents to regulate the cell tissue engineering is a rapidly advancing field that seeks to develop biological materials and devices that can be used in medical applications such as tissue engineering and implantable prosthetics. In a recent report published in Science Advances, researchers in Hong Kong China led by Mingze Sun announced the development of multifunctional tendon-mimetic hydrogels.

Regulating cell morphology and phenotypes with biofunctionalized ACHs. (A) Fluorescence images of F-actin in NIH-3T3 fibroblasts cultured on various substrates (top) and the corresponding angular distribution of cell orientation (bottom) (n ≥ 30). Zero angle (0°) represents the direction parallel to the fiber alignment. Scale bars, 100 μm. (B) AFM images showing the surface topography of biofunctionalized ACH-80 (bottom) and isotropic ANF-PVA hydrogel (top). Scale bars, 1 μm. (C) Fluorescence images of RAW 264.7 macrophages cultured on isotropic ANF-PVA hydrogel (left) and ACH-80 (middle), immunostained for M2 biomarker Arg1, and statistics of the mean fluorescence intensity (MFI) of individual cells showing the differences induced by distinct substrates (right). The cell cultures were treated with IL-4 and IL-13 to induce M2 phenotype. Scale bars, 50 μm. a.u., arbitrary units(D) Immunostaining for iNOS (M1 biomarker) in RAW 264.7 showing the distinct effects induced by isotropic ANF-PVA (left) and ACH-80 (right), also characterized by MFI statistics (right). IFN-γ and LPS were used to induce M1 phenotype. Scale bars, 50 μm. n = 30, ****P < 0.0001. All white arrows indicate the direction parallel to the fiber alignment. Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973
Regulating cell morphology and phenotypes with biofunctionalized ACHs. (A) Fluorescence images of F-actin in NIH-3T3 fibroblasts cultured on various substrates (top) and the corresponding angular distribution of cell orientation (bottom) (n ≥ 30). Zero angle (0°) represents the direction parallel to the fiber alignment. Scale bars, 100 μm. (B) AFM images showing the surface topography of biofunctionalized ACH-80 (bottom) and isotropic ANF-PVA hydrogel (top). Scale bars, 1 μm. (C) Fluorescence images of RAW 264.7 macrophages cultured on isotropic ANF-PVA hydrogel (left) and ACH-80 (middle), immunostained for M2 biomarker Arg1, and statistics of the mean fluorescence intensity (MFI) of individual cells showing the differences induced by distinct substrates (right). The cell cultures were treated with IL-4 and IL-13 to induce M2 phenotype. Scale bars, 50 μm. a.u., arbitrary units(D) Immunostaining for iNOS (M1 biomarker) in RAW 264.7 showing the distinct effects induced by isotropic ANF-PVA (left) and ACH-80 (right), also characterized by MFI statistics (right). IFN-γ and LPS were used to induce M1 phenotype. Scale bars, 50 μm. n = 30, ****P < 0.0001. All white arrows indicate the direction parallel to the fiber alignment. Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973

The researchers sought to develop materials that mimic the complex structure and function of natural tendons. Tendons are tough, fibrous tissues that connect muscles to bones and enable the movement of the musculoskeletal system. The team's hydrogels contained stiff aramid nanofibers and soft polyvinyl alcohol moieties to mimic the interactions between collagen fibers and proteoglycans in natural tendons.


The researchers also biofunctionalized the material surfaces with bioactive molecules to present biophysical cues that mimic the behaviors of cell attachment. In addition, the team integrated soft bioelectronic components onto the hydrogels, which facilitated a variety of physiological benefits. Based on the outstanding functionality of the tendon-mimetics, the team envisioned broader applications of the materials in advanced tissue engineering to form implantable prosthetics for human-machine interactions.


The development of such advanced biomaterials is a significant step towards creating prosthetics that more closely mimic the function of natural tissues. However, it is important to note that further research is needed to fully understand the long-term safety and efficacy of these materials in the human body.

ACHs with integrated multifunctional bioelectronics. (A) Photographs of serpentine electronics transfer-printed onto an isotropic ANF-PVA hydrogel (top) and their stretched state with the processed ACH (bottom). The insets show various functional components. Scale bar, 2 cm. (B) FEA model (left) and microscope image (right) of a representative serpentine device bonded with isotropic ANF-PVA hydrogel. Scale bars, 1 mm. (C) FEA simulation on the stress distribution in the serpentine device under 50% elongation imposed to the hybrid structure. (D and E) ECG (D) and EMG (E) measured with bioelectrodes on a hybrid ACH. (F) Temperature variation in a water bath characterized with a temperature sensor on a hybrid ACH. (G) Schematics and the resistance response to tensile strain for an ionically conductive ACH sample. (H and I) Responses of an ACH-based strain sensor mounted on a finger under various amplitudes of deformation (H) and cyclic motion (I). Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973
ACHs with integrated multifunctional bioelectronics. (A) Photographs of serpentine electronics transfer-printed onto an isotropic ANF-PVA hydrogel (top) and their stretched state with the processed ACH (bottom). The insets show various functional components. Scale bar, 2 cm. (B) FEA model (left) and microscope image (right) of a representative serpentine device bonded with isotropic ANF-PVA hydrogel. Scale bars, 1 mm. (C) FEA simulation on the stress distribution in the serpentine device under 50% elongation imposed to the hybrid structure. (D and E) ECG (D) and EMG (E) measured with bioelectrodes on a hybrid ACH. (F) Temperature variation in a water bath characterized with a temperature sensor on a hybrid ACH. (G) Schematics and the resistance response to tensile strain for an ionically conductive ACH sample. (H and I) Responses of an ACH-based strain sensor mounted on a finger under various amplitudes of deformation (H) and cyclic motion (I). Credit: Science Advances (2023). DOI: 10.1126/sciadv.ade6973

Materials scientists have been working for decades to develop advanced biological materials for medical devices and tissue engineering platforms. The architecture of natural tissues is complex, and it can be difficult to replicate synthetic structures that closely mimic them. In recent years, researchers have made significant progress in developing tendon-mimetic materials with high structural anisotropy.


Sun and colleagues developed an advanced materials platform for their work to construct hybrid anisotropic hydrogels with tendon-like behaviors and multifunctionality at the bio-interfaces. The team established reconfigurable interactions between the stiff and flexible polymers to form a highly oriented framework that emulated a microstructural interplay between aligned collagen fibers and the soft proteoglycans. The biomimetic results of the anisotropic biophysical cues thereby regulated the cell behavior.


The development of anisotropic composite hydrogels by stretching and confining the material consisting of stiff and flexible polymer constituents resulted in a branched microstructure that mimicked collagen-like building blocks. The team observed the characteristic fibrillar network of isotropic hydrogels that resembled hierarchical structures as seen in natural tendons. This was not as feasible with pre-existing synthetic hydrogels.


The scientists biofunctionalized the advanced materials to present a cell adhesion motif such as the arginylglycylaspartic acid motifs to bind with integrins on the cell membrane. The researchers noted the successful biofunctionalization of the advanced materials by observing the adhesion of fibroblast cells on the material surfaces, while samples without surface functionalization did not demonstrate similar cell attachment.


The researchers also demonstrated multimodal physiological sensing by integrating the advanced materials into soft bioelectronics. They used a serpentine design to create wafer-based electronics with high stretchability to withstand the prewashing-drying process of the materials. The team used finite element analysis to assess stress distribution across the device and enhanced the stretchability of the electronic component by modifying its geometrical design for improved mechanical integrity.


Journal Information: Mingze Sun et al, Multifunctional tendon-mimetic hydrogels, Science Advances (2023). DOI: 10.1126/sciadv.ade6973
Jeong-Yun Sun et al, Highly stretchable and tough hydrogels, Nature (2012). DOI: 10.1038/nature11409
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