Integrating perfusable vascular networks with a three-dimensional tissue in a microfluidic device

2017 ◽  
Vol 9 (6) ◽  
pp. 506-518 ◽  
Author(s):  
Yuji Nashimoto ◽  
Tomoya Hayashi ◽  
Itsuki Kunita ◽  
Akiko Nakamasu ◽  
Yu-suke Torisawa ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Microfluidic Device ◽  
Three Dimensional ◽  
Vascular Networks

Creating vascular networks in tissues is crucial for tissue engineering.

scholarly journals Coaxial Electrohydrodynamic Bioprinting of Pre-vascularized Cell-laden Constructs for Tissue Engineering

2021 ◽  
Vol 7 (3) ◽  
Author(s):  
Mao Mao ◽  
Hongtao Liang ◽  
Jiankang He ◽  
Ayiguli Kasimu ◽  
Yanning Zhang ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Feeding Rate ◽  
Three Dimensional ◽  
Vascular Networks ◽  
The Core ◽  
Collagen Hydrogel ◽  
Tissue Constructs ◽  
Vascular Structures ◽  
Living Tissues ◽  
Moving Speed

Recapitulating the vascular networks that maintain the delivery of nutrition, oxygen, and byproducts for the living cells within the three-dimensional (3D) tissue constructs is a challenging issue in the tissue-engineering area. Here, a novel coaxial electrohydrodynamic (EHD) bioprinting strategy is presented to fabricate thick pre-vascularized cell-laden constructs. The alginate and collagen/calcium chloride solution were utilized as the outer-layer and inner-layer bioink, respectively, in the coaxial printing nozzle to produce the core-sheath hydrogel filaments. The effect of process parameters (the feeding rate of alginate and collagen and the moving speed of the printing stage) on the size of core and sheath lines within the printed filaments was investigated. The core-sheath filaments were printed in the predefined pattern to fabricate lattice hydrogel with perfusable lumen structures. Endothelialized lumen structures were fabricated by culturing the core-sheath filaments with endothelial cells laden in the core collagen hydrogel. Multilayer core-sheath filaments were successfully printed into 3D porous hydrogel constructs with a thickness of more than 3 mm. Finally, 3D pre-vascularized cardiac constructs were successfully generated, indicating the efficacy of our strategy to engineer living tissues with complex vascular structures.

scholarly journals 3D Bioprinting of Vascularized Tissues for in vitro and in vivo Applications

2021 ◽  
Vol 9 ◽  
Author(s):  
Earnest P. Chen ◽  
Zeren Toksoy ◽  
Bruce A. Davis ◽  
John P. Geibel
Keyword(s):  
Tissue Engineering ◽  
Drug Testing ◽  
Rapid Development ◽  
Three Dimensional ◽  
3D Bioprinting ◽  
Vascular Networks ◽  
Main Challenge ◽  
3D Printed

With a limited supply of organ donors and available organs for transplantation, the aim of tissue engineering with three-dimensional (3D) bioprinting technology is to construct fully functional and viable tissue and organ replacements for various clinical applications. 3D bioprinting allows for the customization of complex tissue architecture with numerous combinations of materials and printing methods to build different tissue types, and eventually fully functional replacement organs. The main challenge of maintaining 3D printed tissue viability is the inclusion of complex vascular networks for nutrient transport and waste disposal. Rapid development and discoveries in recent years have taken huge strides toward perfecting the incorporation of vascular networks in 3D printed tissue and organs. In this review, we will discuss the latest advancements in fabricating vascularized tissue and organs including novel strategies and materials, and their applications. Our discussion will begin with the exploration of printing vasculature, progress through the current statuses of bioprinting tissue/organoids from bone to muscles to organs, and conclude with relevant applications for in vitro models and drug testing. We will also explore and discuss the current limitations of vascularized tissue engineering and some of the promising future directions this technology may bring.

scholarly journals Accurate Calibration in Multi-Material 3D Bioprinting for Tissue Engineering

Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1402 ◽  
Author(s):  
Enrique Sodupe-Ortega ◽  
Andres Sanz-Garcia ◽  
Alpha Pernia-Espinoza ◽  
Carmen Escobedo-Lucea
Keyword(s):  
Tissue Engineering ◽  
Three Dimensional ◽  
Calibration Method ◽  
3D Bioprinting ◽  
Vascular Networks ◽  
Single Session ◽  
Systems And Control ◽  
Complex Relationships ◽  
And Control ◽  
Printing Parameters

Most of the studies in three-dimensional (3D) bioprinting have been traditionally based on printing a single bioink. Addressing the complexity of organ and tissue engineering, however, will require combining multiple building and sacrificial biomaterials and several cells types in a single biofabrication session. This is a significant challenge, and, to tackle that, we must focus on the complex relationships between the printing parameters and the print resolution. In this paper, we study the influence of the main parameters driven multi-material 3D bioprinting and we present a method to calibrate these systems and control the print resolution accurately. Firstly, poloxamer hydrogels were extruded using a desktop 3D printer modified to incorporate four microextrusion-based bioprinting (MEBB) printheads. The printed hydrogels provided us the particular range of printing parameters (mainly printing pressure, deposition speed, and nozzle z-offset) to assure the correct calibration of the multi-material 3D bioprinter. Using the printheads, we demonstrated the excellent performance of the calibrated system extruding different fluorescent bioinks. Representative multi-material structures were printed in both poloxamer and cell-laden gelatin-alginate bioinks in a single session corroborating the capabilities of our system and the calibration method. Cell viability was not significantly affected by any of the changes proposed. We conclude that our proposal has enormous potential to help with advancing in the creation of complex 3D constructs and vascular networks for tissue engineering.

scholarly journals Microvascular Guidance: A Challenge to Support the Development of Vascularised Tissue Engineering Construct

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Irza Sukmana
Keyword(s):  
Tissue Engineering ◽  
Three Dimensional ◽  
Artificial Organ ◽  
Vascular Networks ◽  
Tissue Constructs ◽  
Future Challenges ◽  
Engineered Tissue ◽  
And Function ◽  
Tissue Construct

The guidance of endothelial cell organization into a capillary network has been a long-standing challenge in tissue engineering. Some research efforts have been made to develop methods to promote capillary networks inside engineered tissue constructs. Capillary and vascular networks that would mimic blood microvessel function can be used to subsequently facilitate oxygen and nutrient transfer as well as waste removal. Vascularization of engineering tissue construct is one of the most favorable strategies to overpass nutrient and oxygen supply limitation, which is often the major hurdle in developing thick and complex tissue and artificial organ. This paper addresses recent advances and future challenges in developing three-dimensional culture systems to promote tissue construct vascularization allowing mimicking blood microvessel development and function encounteredin vivo. Bioreactors systems that have been used to create fully vascularized functional tissue constructs will also be outlined.

scholarly journals Direct Bioprinting of Vessel-Like Tubular Microfluidic Channels

2013 ◽  
Vol 4 (2) ◽  
Author(s):  
Yahui Zhang ◽  
Yin Yu ◽  
Ibrahim T. Ozbolat
Keyword(s):  
Tissue Engineering ◽  
Complex Structure ◽  
Three Dimensional ◽  
Microfluidic Channel ◽  
Great Promise ◽  
Microfluidic Channels ◽  
Vascular Networks ◽  
Channel Network ◽  
Organ Printing ◽  
Chitosan Hydrogels

Despite the progress in tissue engineering, several challenges must be addressed for organ printing to become a reality. The most critical challenge is the integration of a vascular network, which is also a problem that the majority of tissue engineering technologies are facing. An embedded microfluidic channel network is probably the most promising solution to this problem. However, the available microfluidic channel fabrication technologies either have difficulty achieving a three-dimensional complex structure or are difficult to integrate within cell printing process in tandem. In this paper, a novel printable vessel-like microfluidic channel fabrication method is introduced that enables direct bioprinting of cellular microfluidic channels in form of hollow tubes. Alginate and chitosan hydrogels were used to fabricate microfluidic channels showing the versatility of the process. Geometric characterization was performed to understand effect of biomaterial and its flow rheology on geometric properties. Microfluidic channels were printed and embedded within bulk hydrogel to test their functionality through perfusion of cell type oxygenized media. Cell viability experiments were conducted and showed great promise of the microfluidic channels for development of vascular networks.

HYDROXYAPATITE, ALGINATE, AND CHITOSAN FOR BONE SCAFFOLDS: SPECTROSCOPY STUDY

2016 ◽  
Vol 19 (2) ◽  
pp. 93-100
Author(s):  
Lalita El Milla
Keyword(s):  
Tissue Engineering ◽  
Bone Tissue Engineering ◽  
Bone Tissue ◽  
Functional Groups ◽  
Bone Growth ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
Tissue Engineering Scaffolds ◽  
Hydroxyapatite Powder ◽  
Materials Used

Scaffolds is three dimensional structure that serves as a framework for bone growth. Natural materials are often used in synthesis of bone tissue engineering scaffolds with respect to compliance with the content of the human body. Among the materials used to make scafffold was hydroxyapatite, alginate and chitosan. Hydroxyapatite powder obtained by mixing phosphoric acid and calcium hydroxide, alginate powders extracted from brown algae and chitosan powder acetylated from crab. The purpose of this study was to examine the functional groups of hydroxyapatite, alginate and chitosan. The method used in this study was laboratory experimental using Fourier Transform Infrared (FTIR) spectroscopy for hydroxyapatite, alginate and chitosan powders. The results indicated the presence of functional groups PO43-, O-H and CO32- in hydroxyapatite. In alginate there were O-H, C=O, COOH and C-O-C functional groups, whereas in chitosan there were O-H, N-H, C=O, C-N, and C-O-C. It was concluded that the third material containing functional groups as found in humans that correspond to the scaffolds material in bone tissue engineering.

In vitro Three Dimensional Scaffold-free Construct of Human Adipose-derived Stem Cells in Coculture with Endothelial Cells and Fibroblasts

2017 ◽  
Vol 68 (6) ◽  
pp. 1341-1344
Author(s):  
Grigore Berea ◽  
Gheorghe Gh. Balan ◽  
Vasile Sandru ◽  
Paul Dan Sirbu
Keyword(s):  
Tissue Engineering ◽  
Stem Cells ◽  
Endothelial Cells ◽  
Single Cell ◽  
Cell Line ◽  
Bone Repair ◽  
Umbilical Vein ◽  
Human Fibroblasts ◽  
Three Dimensional ◽  
Adipose Derived Stem Cells

Complex interactions between stem cells, vascular cells and fibroblasts represent the substrate of building microenvironment-embedded 3D structures that can be grafted or added to bone substitute scaffolds in tissue engineering or clinical bone repair. Human Adipose-derived Stem Cells (hASCs), human umbilical vein endothelial cells (HUVECs) and normal dermal human fibroblasts (NDHF) can be mixed together in three dimensional scaffold free constructs and their behaviour will emphasize their potential use as seeding points in bone tissue engineering. Various combinations of the aforementioned cell lines were compared to single cell line culture in terms of size, viability and cell proliferation. At 5 weeks, viability dropped for single cell line spheroids while addition of NDHF to hASC maintained the viability at the same level at 5 weeks Fibroblasts addition to the 3D construct of stem cells and endothelial cells improves viability and reduces proliferation as a marker of cell differentiation toward osteogenic line.

scholarly journals Advances in tissue engineering of vasculature through three‐dimensional bioprinting

2021 ◽  
Author(s):  
Junjin Zhu ◽  
Yuting Wang ◽  
Linna Zhong ◽  
Fangwei Pan ◽  
Jian Wang
Keyword(s):  
Tissue Engineering ◽  
Three Dimensional

scholarly journals Development of a human neuromuscular tissue-on-a-chip model on a 24-well-plate-format compartmentalized microfluidic device

Lab on a Chip ◽  
2021 ◽  
Author(s):  
Kazuki Yamamoto ◽  
Nao Yamaoka ◽  
Yu Imaizumi ◽  
Takunori Nagashima ◽  
Taiki Furutani ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Microfluidic Device ◽  
Motor Neurons ◽  
Muscle Fibers ◽  
Three Dimensional ◽  
Tissue Model ◽  
Skeletal Muscle Fibers

A three-dimensional human neuromuscular tissue model that mimics the physically separated structures of motor neurons and skeletal muscle fibers is presented.

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