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Open AccessJournal ArticleDOI

The Role of the Microenvironment in Controlling the Fate of Bioprinted Stem Cells.

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TLDR
This review will examine the methods through which bioprinted stem cells are differentiated into desired cell lineages through biochemical, biological, and biomechanical techniques.
Abstract
The field of tissue engineering and regenerative medicine has made numerous advances in recent years in the arena of fabricating multifunctional, three-dimensional (3D) tissue constructs This can be attributed to novel approaches in the bioprinting of stem cells There are expansive options in bioprinting technology that have become more refined and specialized over the years, and stem cells address many limitations in cell source, expansion, and development of bioengineered tissue constructs While bioprinted stem cells present an opportunity to replicate physiological microenvironments with precision, the future of this practice relies heavily on the optimization of the cellular microenvironment To fabricate tissue constructs that are useful in replicating physiological conditions in laboratory settings, or in preparation for transplantation to a living host, the microenvironment must mimic conditions that allow bioprinted stem cells to proliferate, differentiate, and migrate The advances of bioprinting stem cells and directing cell fate have the potential to provide feasible and translatable approach to creating complex tissues and organs This review will examine the methods through which bioprinted stem cells are differentiated into desired cell lineages through biochemical, biological, and biomechanical techniques

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Citations
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Journal ArticleDOI

A photo-crosslinkable cartilage-derived extracellular matrix bioink for auricular cartilage tissue engineering.

TL;DR: The results showed cdCEM was obtained with complete removal of cellular components while preserving major ECM proteins, and the potential of cell-based bioprinting using this cartilage-specific dECMMA bioink is demonstrated as an alternative option for auricular cartilage reconstruction.
Journal ArticleDOI

DNA-Based Dynamic Mimicry of Membrane Proteins for Programming Adaptive Cellular Interactions.

TL;DR: In this article, a cell-surface nano-architecture that realizes molecular-recognition-initiated DNA assembly to mimic the dynamic behavior of membrane proteins, enabling the manipulation of cellular interaction in response to environmental changes.
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Using bioprinting and spheroid culture to create a skin model with sweat glands and hair follicles.

TL;DR: In this article, a combined model was created by seeding hair follicles on 3D printed sweat glands and hair spheroids, and the interaction between SG scaffolds and HF spheroid was detected using RNA expression and immunofluorescence staining.
Journal ArticleDOI

Bioprinting and regeneration of auricular cartilage using a bioactive bioink based on microporous photocrosslinkable acellular cartilage matrix

TL;DR: In this article , a biomimetic microporous methacrylate-modified acellular cartilage matrix (ACMMA) was used for the development of biological auricle equivalents with precise shapes, low immunogenicity, and excellent mechanics using auricular chondrocytes.
References
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Journal ArticleDOI

Hydrogels that mimic developmentally relevant matrix and N-cadherin interactions enhance MSC chondrogenesis

TL;DR: The inherent biologic activity of HA-based hydrogels, as well as the promise of biofunctionalizing HA hydrogel to emulate the complexity of the natural cell microenvironment during embryogenesis, are demonstrated, particularly in stem cell-based cartilage regeneration.
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Cardiac tissue engineering using tissue printing technology and human cardiac progenitor cells.

TL;DR: This study evaluated the combination of TP, human cardiac-derived cardiomyocyte progenitor cells (hCMPCs) and biomaterials to obtain a construct with cardiogenic potential for in vitro use or in vivo application and showed that printing can be used for defined cell delivery, while retaining functional properties.
Journal ArticleDOI

Bio-printing of collagen and VEGF-releasing fibrin gel scaffolds for neural stem cell culture.

TL;DR: The results demonstrated that bio-printing of VEGF-containing fibrin gel supported sustained release of the GF in the collagen scaffold, and can be gainfully used in the development of three-dimensional (3D) artificial tissue assays and neural tissue regeneration applications.
Journal ArticleDOI

Hydrogels with Time-Dependent Material Properties Enhance Cardiomyocyte Differentiation In Vitro

TL;DR: Though ester hydrolysis does not substantially alter hydrogel stiffening over 2 weeks in vitro, model predictions indicate that ester Hydrolysis will eventually degrade the material with additional time, implying that this hydrogels may be appropriate for in vivo applications where temporally changing material properties enhance cell maturation prior to its replacement with host tissue.
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