
Introduction to Tissue Engineering
Description
Alles über E-Books | Antworten auf Fragen rund um E-Books, Kopierschutz und Dateiformate finden Sie in unserem Info- & Hilfebereich.
More details
Other editions
Additional editions

Person
Content
Preface xiii
Acknowledgments xv
List of Abbreviations xvii
Important Terminology and Concepts xxi
1 Introduction to Tissue Engineering 1
1.1 Introduction to Tissue Engineering, 2
1.2 Chronic Shortage of Donor Organs, 3
1.3 The Tissue Engineering Paradigm, 4
1.4 Definition of Tissue Engineering, 5
1.5 Process of Bioengineering 3D Artificial Tissue, 9
1.6 Design Principles for Tissue Engineering, 12
1.7 Building Blocks of Tissue Engineering, 14
1.8 Scientific and Technological Challenges, 15
1.9 Functional Assessment of Artificial Tissue, 16
1.10 Seminal Papers in Tissue Engineering, 18
1.11 Applications of 3D Artificial Tissue, 20
1.12 Two-Dimensional Versus Three-Dimensional Culture, 22
1.13 Integration of Core Technologies, 22
1.14 Growth of Tissue Engineering, 24
1.15 Disciplines in Tissue Engineering, 26
1.16 Tissue Engineering and Related Fields, 28
Summary, 33
Practice Questions, 34
References, 35
2 Cells for Tissue Engineering 40
2.1 Cells and Tissue Engineering, 41
2.2 Cell Structure and Function, 43
2.3 The Dynamic Extracellular Matrix, 47
2.4 Cell Signaling, 48
2.5 Cellular Junctions, 50
2.6 Mammalian Tissue and Artificial Tissue, 52
2.7 Cell Sourcing, 52
2.8 The Cell Transplantation Process, 55
2.9 Cells for Cell Transplantation, 58
2.10 Mode of Action of Cells During Cell Transplantation, 59
2.11 Cell Transplantation and Tissue Engineering, 60
2.12 The Cell Culture Process, 61
2.13 Applications of Monolayer 2D Cell Culture, 64
2.14 Cell Culture Versus Tissue Engineering, 65
2.15 Introduction to Stem Cell Engineering, 66
2.16 Human Embryonic Stem Cells, 70
2.17 Induced Pluripotent Stem Cells, 71
2.18 Adult Stem Cells, 72
Summary, 72
Practice Questions, 73
References, 74
3 Biomaterials for Tissue Engineering 84
3.1 Definition of Biomaterials, 85
3.2 Scheme for Biomaterial Development, 88
3.3 Historical Perspective on Biomaterials, 90
3.4 Tensile Properties, 92
3.5 Modulation of Tensile Properties, 95
3.6 Material Degradation, 97
3.7 Biocompatibility, 100
3.8 Biomimetic Biomaterial, 104
3.9 Classification of Biomaterials, 106
3.10 Biomaterial Platforms, 108
3.11 Smart Materials, 113
3.12 The Dynamic Extracellular Matrix, 114
3.13 Idealized Biomaterial, 116
Summary, 118
Practice Questions, 119
References, 121
4 Tissue Fabrication Technology 130
4.1 Introduction to Tissue Fabrication Technologies, 131
4.2 Self-Organization Technology, 133
4.3 Cell Sheet Engineering, 135
4.4 Scaffold-Based Tissue Fabrication, 137
4.5 Cell and Organ Printing, 140
4.6 Solid Freeform Fabrication, 142
4.7 Soft Lithography and Microfluidics, 143
4.8 Cell Patterning, 145
4.9 Idealized System to Support Tissue Fabrication, 148
Summary, 149
Practice Questions, 150
References, 151
5 Vascularization of Artificial Tissue 156
5.1 Introduction, 157
5.2 Seminal Publications in Angiogenesis Research, 159
5.3 Vascularization Defined, 160
5.4 Molecular Mechanism of Vasculogenesis, 161
5.5 Molecular Mechanism of Angiogenesis, 163
5.6 Molecular Mechanism of Arteriogenesis, 164
5.7 Therapeutic Angiogenesis, 166
5.8 Tissue Engineering and Vascularization, 167
5.9 Conceptual Framework for Vascularization During Artificial Tissue Formation, 169
5.10 In Vivo Models of Vascularization, 172
5.11 Idealized Vascularization Strategy for Tissue Engineering, 174
5.12 Flow Chart and Decision Making, 176
5.13 Biologically Replicated Vascularization Strategies, 179
5.14 Biologically Mediated Vascularization Strategies, 181
5.15 Biologically Inspired Vascularization Strategies, 184
Summary, 186
Practice Questions, 187
References, 188
6 Bioreactors for Tissue Engineering 193
6.1 Introduction to Bioreactors, 194
6.2 Bioreactors Defined, 195
6.3 Classification of Bioreactors, 197
6.4 Design Considerations, 200
6.5 Idealized Bioreactor System, 202
6.6 Bioreactors and Tissue Engineering, 205
6.7 Bioreactors for Mammalian Cell Culture, 207
6.8 Bioreactors for Scaffold Fabrication, 209
6.9 Bioreactors for Scaffold Cellularization, 212
6.10 Perfusion Systems, 215
6.11 Bioreactors for Stretch, 219
6.12 Electrical Stimulation, 221
Summary, 226
Practice Questions, 227
References, 230
7 Tracheal Tissue Engineering 237
7.1 Structure and Function of the Trachea, 238
7.2 Congenital Tracheal Stenosis, 240
7.3 Genetic Regulation of Tracheal Development, 241
7.4 Post Intubation and Post Tracheostomy Tracheal Stenosis, 243
7.5 Treatment Modalities for Tracheal Stenosis, 245
7.6 Design Considerations for Tracheal Tissue Engineering, 247
7.7 Process of Bioengineering Artificial Tracheas, 247
7.8 Tissue Engineering Models for Artificial Tracheas, 250
7.9 Tracheal Tissue Engineering-An Example of a Clinical Study, 253
7.10 Tracheal Tissue Engineering-A Second Example of a Clinical Study, 255
Summary, 258
Practice Questions, 258
References, 260
8 Bladder Tissue Engineering 265
8.1 Bladder Structure and Function, 266
8.2 Neurogenic Bladder Dysfunction, 267
8.3 Surgical Bladder Augmentation, 269
8.4 Development of the Urinary Bladder, 270
8.5 Design Considerations for Bladder Tissue Engineering, 270
8.6 Process of Bioengineering Artificial Bladders, 271
8.7 Cell Sheet Engineering for Bladder Tissue Engineering, 273
8.8 Small Intestinal Submucosa (SIS) for Bladder Tissue Engineering, 275
8.9 Plga as a Biomaterial for Bladder Tissue Engineering, 278
8.10 Acellular Grafts for Bladder Tissue Engineering, 280
8.11 Organ Models for Bladder Tissue Engineering, 283
8.12 Clinical Study for Bladder Tissue Engineering, 284
Summary, 285
Practice Questions, 286
References, 288
9 Liver Tissue Engineering 295
9.1 Structure and Function of the Liver, 296
9.2 Acute Liver Failure, 297
9.3 Liver Transplantation, 299
9.4 Liver Regeneration, 301
9.5 Liver Development, 302
9.6 Design Considerations for Liver Tissue Engineering, 303
9.7 Process of Bioengineering Artificial Liver Tissue, 303
9.8 Stem Cells for Liver Tissue Engineering, 305
9.9 Surface Patterning Technology for Liver Tissue Engineering, 307
9.10 Biomaterial Platforms for Liver Tissue Engineering, 309
9.11 Fabrication of 3D Artificial Liver Tissue, 309
9.12 Vascularization for Liver Tissue Engineering, 311
9.13 Bioreactors for Liver Tissue Engineering, 312
9.14 Spheroid Culture for Liver Tissue Engineering, 313
Summary, 314
Practice Questions, 315
References, 317
Index 323
Important Terminology and Concepts
- TISSUE ENGINEERING—Tissue engineering is a multidisciplinary field bringing together experts from engineering, life sciences and medicine, utilizing the building blocks of cells, biomaterials and bioreactors for the development of 3D artificial tissue and organs which can be used to augment, repair and/or replace damaged and/or diseased tissue.
- CELL-MATRIX INTERACTIONS—When a cell sees any given ECM protein, the cell scans the protein molecule to identify specific binding sites for which it has integrins; for example, the integrin α5β1 binds to the RGD site of the fibronectin molecule. Although the fibronectin molecule is large, there is only a sequence of three amino acids that are recognized by cells having the α5β1 integrin; the binding of the α5β1 integrin to the RGD site on the fibronectin molecule is referred to as a specific cell-matrix interaction.
- CELL-CELL INTERACTIONS—Cells communicate with other cells via cell-cell interactions, and these are critical in maintaining cell phenotype and tissue function. There are 4 types of cell signaling, known as endocrine, paracrine, autocrine, and contact-dependent signaling. In addition, cellular junctions provide various functions at the cell-cell; gap junctions are one example. The functional coupling of cells with other cells is known as cell-cell interaction.
- AUTOLOGOUS CELLS—Autologous cells are cells that have been isolated from a tissue biopsy of the person who will also be recipient of these cells; the donor and recipient for autologous cells is the same.
- ALLOGENEIC CELLS—Allogeneic cells are isolated from a donor and then transplanted into a recipient patient, with the donor and recipient being different people.
- CELL TRANSPLANTATION—Cell transplantation has been defined as the process by which cells are delivered to the site of injury in order to improve the functional performance of injured tissue. Whole blood transfusions, packed red cell transfusions, platelet transfusions, and bone marrow transplants are examples of cell therapy.
- STEM CELL TRANSPLANTATION—Stem cell transplantation is a specialized case of cell transplantation, in which the cells being delivered are stem cells. Use of embryonic stem cells, induced pluripotent stem cells, and adult stem cells fall under the classification of stem cell transplantation.
- CENTRAL DOGMA OF MOLECULAR BIOLOGY—The central dogma of molecular biology states that DNA is transcribed to RNA, which is then translated to proteins.
- CHARACTERISTICS OF STEM CELLS—Stem cells have three important characteristics that distinguish them from other cell types: self-renewal, unspecialized function, and differentiation potential.
- CELL POTENCY—Cell potency refers to the differentiation potential of stem cells.
- BIOMATERIALS—A biomaterial is any substance that simulates the extracellular matrix by functionally interacting with isolated cells to support fabrication and maturation of 3D artificial tissue.
- TENSILE PROPERTIES OF BIOMATERIALS—The tensile properties of a material are used very frequently in engineering design as an important criterion for material selection. The tensile properties of a material provide information about the strength of the material, its ability to withstand a particular load, and information about elastic properties. All of these properties are extremely important for material selection during tissue fabrication.
- BIOMATERIAL DEGRADATION—Biomaterial degradation refers to the gradual breakdown of a biomaterial mediated in a controlled manner to support the fabrication of 3D artificial tissue
- BIOMATERIAL BIOCOMPATIBILITY—The ability of 3D artificial tissue to be accepted by host defense mechanisms upon implantation, while maintaining functional capacity, is known as biocompatibility.
- BIOMIMETIC BIOMATERIALS—A two-part definition of biomimetic biomaterials has been provided in a recent article: 1) The development of biomaterials for tissue engineering applications has recently focused on the design of biomimetic materials that are able to interact with surrounding tissues by biomolecular recognition, 2) The design of biomimetic materials is an attempt to make the materials such that they are capable of eliciting specific cellular responses and directing new tissue formation mediated by specific interactions, which can be manipulated by altering design parameters instead of by non-specifically adsorbed ECM proteins.
- CLASSIFICATION OF BIOMATERIALS—Biomaterials are frequently classified based on source (natural and synthetic), based on degradation (biodegradable and non-biodegradable), and based on interatomic bonding forces (metals, polymers, and ceramics).
- BIOMATERIAL PLATFORMS—There are four platforms that have been widely used for tissue engineering applications: polymeric scaffolds, biodegradable hydrogels, decellular matrices, and self-organization strategies.
- DECELLULARIZED MATICES—This strategy is based on the utilization of naturally occurring extracellular matrix as the scaffolding material for 3D tissue formation. Tissue specimens are obtained from cadaveric or xenogeneic sources, and cells are completely removed using one of several potential strategies. Removal of cellular components from tissue specimens is known as decellularization, and the material that is obtained after removal of the cells is known as an acellular scaffold.
- HYRDOGELS—The term hydrogel is composed of “hydro” (water) and “gel,” and refers to aqueous (water-containing) gels. To be more precise, it refers to polymer networks that are insoluble in water; they swell to an equilibrium volume but retain their shapes.
- POLYMERS—Polymers can be viewed as molecules of a high molecular weight that are composed of repeating monomer units.
- SELF-ORGANIZATION STRATEGIES—Self-organization is prevalent in biological systems; it involves the physical interaction of molecules in a steady-state structure. In a broad sense, self-organization can be viewed as a process that occurs in the absence of any constraining conditions, thereby providing a greater degree of freedom and flexibility.
- SMART MATERIALS—The most recent generation of biomaterials has been designed to respond to changes in the cellular environment. These materials, known as smart materials, are receptive to changes in the physiological environment and are adaptive to changes in the degree of tissue maturation.
- TISSUE FABRICATION TECHNOLOGIES—Tissue fabrication technologies can be classified into six categories, which include scaffold-free methods, cell patterning techniques, scaffold-based methods, rapid prototyping technologies, printing technology, and “organ-on-a-chip” models.
- SELF-ORGANIZATION TECHNOLOGY—Self-organization technology is based on the fabrication of extracellular matrix by cells that then use the newly formed ECM to support artificial tissue fabrication. This technology is an example of a scaffold-free tissue fabrication process and does not require external or synthetic scaffolding; rather, scaffolding is produced by cells.
- CELL PRINTING—Bioprinting process used for 2D cell patterning by depositing bio-ink on the surface of biopaper.
- ORGAN PRINTING—Bioprinting process used for fabrication of 3D tissue by depositing bio-ink on the surface of biopaper.
- SOLID FREEFORM FABRICATION—Solid freeform fabrication refers to a group of technologies that build 3D scaffolds using a layer-by-layer approach. Collectively, these technologies are known as rapid prototyping methods.
- SOFT LITHOGRAPHY—Soft lithography is a microfabrication technology used to engineer microfluidic devices, particularly microvascular networks.
- CELL PATTERNING—The process by which the spatial placement of cells is controlled to create an organized pattern of cell monolayers or 3D tissue is known as cell patterning.
- VASCULOGENESIS—Vasculogenesis refers to initial events in vascular growth in which endothelial cell precursors (angioblasts) migrate to discrete locations, differentiate in situ, and assemble into solid endothelial cords, later forming a plexus with endothelial tubes.
- ANGIOGENESIS—Angiogenesis refers to the growth, expansion, and remodeling of primitive blood vessels formed during vasculogenesis to form a mature vascular network.
- ARTERIOGENESIS—Arteriogenesis is the process by which blood vessels increase in diameter to form muscular arteries and incorporate smooth muscle cells and vaso-contraction and vaso-relaxation properties.
- THERAPEUTIC ANGIOGENESIS—Therapeutic angiogenesis refers to the stimulation of angiogenesis for therapeutic purposes.
- BIOLOGICALLY REPLICATED VASCULARIZATION STRATEGIES—Biologically replicated processes are influenced by molecular biology, with the objective being the understanding of biological phenomena and defining...
System requirements
File format: ePUB
Copy protection: Adobe-DRM (Digital Rights Management)
System requirements:
- Computer (Windows; MacOS X; Linux): Install the free reader Adobe Digital Editions prior to download (see eBook Help).
- Tablet/smartphone (Android; iOS): Install the free app Adobe Digital Editions or the app PocketBook before downloading (see eBook Help).
- E-reader: Bookeen, Kobo, Pocketbook, Sony, Tolino and many more (not Kindle).
The file format ePub works well for novels and non-fiction books – i.e., „flowing” text without complex layout. On an e-reader or smartphone, line and page breaks automatically adjust to fit the small displays.
This eBook uses Adobe-DRM, a „hard” copy protection. If the necessary requirements are not met, unfortunately you will not be able to open the eBook. You will therefore need to prepare your reading hardware before downloading.
Please note: We strongly recommend that you authorise using your personal Adobe ID after installation of any reading software.
For more information, see our ebook Help page.