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The placenta plays a vital role in pregnancy by regulating selective exchange between maternal and fetal circulations and producing essential hormonal signals. Here, we present an in vitro placenta-on-a-chip platform that leverages 3D bioprinting to replicate the structural and functional features of the human placental barrier. This microengineered system utilizes digital light processing 3D bioprinting to fabricate the microfluidic mold and to construct 3D encapsulated cell cultures within a biomimetic hydrogel scaffold, enabling co-culture of three human cell types, including two derived from primary placental tissue. We demonstrate excellent cell viability, high metabolic activity, placental hormone secretion, and native-like selective barrier transport properties within the model. This system offers a versatile platform for experimental perturbations to explore mechanisms of normal placental function and identify contributors to placental dysfunction. 

Abstract Bioprinting of cell-laden hydrogels is a rapidly growing field in tissue engineering. The advent of digital light processing (DLP) three-dimensional (3D) bioprinting technique has revolutionized the fabrication of complex 3D structures. By adjusting light exposure, it becomes possible to control the mechanical properties of the structure, a critical factor in modulating cell activities. To better mimic cell densities in real tissues, recent progress has been made in achieving high-cell-density (HCD) printing with high resolution. However, regulating the stiffness in HCD constructs remains challenging. The large volume of cells greatly affects the light-based DLP bioprinting by causing light absorption, reflection, and scattering. Here, we introduce a neural network-based machine learning technique to predict the stiffness of cell-laden hydrogel scaffolds. Using comprehensive mechanical testing data from 3D bioprinted samples, the model was trained to deliver accurate predictions. To address the demand of working with precious and costly cell types, we employed various methods to ensure the generalizability of the model, even with limited datasets. We demonstrated a transfer learning method to achieve good performance for a precious cell type with a reduced amount of data. The chosen method outperformed many other machine learning techniques, offering a reliable and efficient solution for stiffness prediction in cell-laden scaffolds. This breakthrough paves the way for the next generation of precision bioprinting and more customized tissue engineering. 

Anthropogenic stressors pose substantial threats to the existence of coral reefs. Achieving successful coral recruitment stands as a bottleneck in reef restoration and hybrid reef engineering efforts. Here, we enhance coral settlement through the development of biomimetic microhabitats that replicate the chemical landscape of healthy reefs. We engineered a soft biomaterial, SNAP-X, comprising silica nanoparticles (NPs), biopolymers, and algal exometabolites, to enrich reef microhabitats with bioactive molecules from crustose coralline algae (CCA). Coral settlement was enhanced over 20-fold using SNAP-X-coated substrates compared with uncoated controls. SNAP-X is designed to release chemical signals slowly (>1 month) under natural seawater conditions, and can be rapidly applied to natural reef substrates via photopolymerization, facilitating the light-assisted 3D printing of microengineered habitats. We anticipate that these biomimetic chemical microhabitats will be widely used to augment coral settlement on degraded reefs and to support ecosystem processes on hybrid reefs. 

Workflow for developing anin vitrobiomimetic myotendinous junction (MTJ): tissue properties and SEM data are measured (left), informing 3D printing of microstructure and properties (middle). MTJ formation occurs naturally within 2 weeks (right). 

Abstract Controllable and long‐term release remains a great challenge in current drug delivery systems. Benefiting from their efficient drug loading and painless administration, microneedles (MNs) have emerged as a promising platform for transdermal drug delivery, while they often fail to achieve long‐term tissue adhesion and controllable extended drug release. Here, 3D printing of an innovative MN patch is presented with succulent‐inspired responsive microstructures and light‐controllable long‐term release capability. The MN exhibits a reversible shrink‐swell volume change behavior in response to surrounding humidity, which enables sufficient mechanical strength for skin penetration under the shrinkage conditions and efficient long‐term adhesion when swollen in skin tissues. Moreover, the MN patch introduces a controllable long‐term drug release system, achieved through the integration of thiolated heparin (Hep‐SH) for sustained growth factor release and graphene oxide (GO) nanosheets for controlled drug release via near infrared (NIR) laser irradiation. The MN patches with growth factor loading have good biocompatibility and can promote the proliferation, migration, and proangiogenesis of endothelial cells is further demonstrated. Thus, it is believed that such flexible MN patches can be promising candidates for controllable long‐term transdermal drug delivery as well as other related tissue engineering applications. 

Abstract The field of engineered living materials lies at the intersection of materials science and synthetic biology with the aim of developing materials that can sense and respond to the environment. In this study, we use 3D printing to fabricate a cyanobacterial biocomposite material capable of producing multiple functional outputs in response to an external chemical stimulus and demonstrate the advantages of utilizing additive manufacturing techniques in controlling the shape of the fabricated photosynthetic material. As an initial proof-of-concept, a synthetic riboswitch is used to regulate the expression of a yellow fluorescent protein reporter inSynechococcus elongatusPCC 7942 within a hydrogel matrix. Subsequently, a strain ofS. elongatusis engineered to produce an oxidative laccase enzyme; when printed within a hydrogel matrix the responsive biomaterial can decolorize a common textile dye pollutant, indigo carmine, potentially serving as a tool in environmental bioremediation. Finally, cells are engineered for inducible cell death to eliminate their presence once their activity is no longer required, which is an important function for biocontainment and minimizing environmental impact. By integrating genetically engineered stimuli-responsive cyanobacteria in volumetric 3D-printed designs, we demonstrate programmable photosynthetic biocomposite materials capable of producing functional outputs including, but not limited to, bioremediation.