RESUMEN
The journey of a hematopoietic stem cell (HSC) involves the passage through successive anatomical sites where HSCs are in direct contact with their surrounding microenvironment, also known as niche. These spatial and temporal cellular interactions throughout development are required for the acquisition of stem cell properties, and for maintaining the HSC pool through balancing self-renewal, quiescence and lineage commitment. Understanding the context and consequences of these interactions will be imperative for our understanding of HSC biology and will lead to the improvement of in vitro production of HSCs for clinical purposes. The aorta-gonad-mesonephros (AGM) region is in this light of particular interest since this is the cradle of HSC emergence during the embryonic development of all vertebrate species. In this review, we will focus on the developmental origin of HSCs and will discuss the novel technological approaches and recent progress made to identify the cellular composition of the HSC supportive niche and the underlying molecular events occurring in the AGM region.
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Genómica/tendencias , Hematopoyesis/genética , Células Madre Hematopoyéticas/fisiología , Análisis de la Célula Individual/tendencias , Nicho de Células Madre , Animales , Aorta/embriología , Técnicas de Cultivo de Célula/tendencias , Linaje de la Célula , Células Cultivadas , Difusión de Innovaciones , Perfilación de la Expresión Génica/tendencias , Regulación del Desarrollo de la Expresión Génica , Gónadas/embriología , Humanos , Mesonefro/embriología , Fenotipo , Proteómica/tendencias , Transducción de Señal , TranscriptomaAsunto(s)
Investigación Biomédica , Técnicas de Cultivo de Célula , Desarrollo de Medicamentos , Descubrimiento de Drogas , Industria Farmacéutica , Fenómenos Fisiológicos/efectos de los fármacos , Investigación Biomédica/métodos , Investigación Biomédica/organización & administración , Técnicas de Cultivo de Célula/instrumentación , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Técnicas de Cocultivo , Desarrollo de Medicamentos/métodos , Descubrimiento de Drogas/métodos , Descubrimiento de Drogas/tendencias , Industria Farmacéutica/métodos , Industria Farmacéutica/organización & administración , Humanos , Colaboración Intersectorial , MiniaturizaciónRESUMEN
The retina is a complex neuronal structure that converts light energy into visual perception. Many specialized aspects of the primate retina, including a cone rich macula for high acuity vision, ocular size, and cell type diversity are not found in other animal models. In addition, the unique morphologies and distinct laminar positions of cell types found in the retina make this model system ideal for the study of neuronal cell fate specification. Many key early events of human retinal development are inaccessible to investigation as they occur during gestation. For these reasons, it has been necessary to develop retinal model systems to gain insight into human-specific retinal development and disease. Recent advances in culturing retinal tissue have generated new systems for retinal research and have moved us closer to generating effective regenerative therapies for vision loss. Here, we describe the strengths, weaknesses, and future directions for different human retinal model systems including dissociated primary tissue, explanted primary tissue, retinospheres, and stem cell-derived retinal organoids.
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Técnicas de Cultivo de Célula/tendencias , Retina/metabolismo , Retina/fisiología , Técnicas de Cultivo de Célula/métodos , Diferenciación Celular/fisiología , Humanos , Células Madre Pluripotentes Inducidas , Modelos Biológicos , Organoides/metabolismo , Cultivo Primario de Células/métodos , Células Fotorreceptoras Retinianas Conos/metabolismo , Degeneración Retiniana/metabolismoRESUMEN
Organoids have complex three-dimensional structures that exhibit functionalities and feature architectures similar to those of in vivo organs and are developed from adult stem cells, embryonic stem cells, and pluripotent stem cells through a self-organization process. Organoids derived from adult epithelial stem cells are the most mature and extensive. In recent years, using organoid culture techniques, researchers have established various adult human tissue-derived epithelial organoids, including intestinal, colon, lung, liver, stomach, breast, and oral mucosal organoids, all of which exhibit strong research and application prospects. Studies have shown that epithelial organoids are mainly applied in drug discovery, personalized drug response testing, disease mechanism research, and regenerative medicine. In this review, we mainly discuss current organoid culture systems and potential applications of this technique with human epithelial tissue.
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Células Madre Adultas/citología , Técnicas de Cultivo de Célula/métodos , Evaluación Preclínica de Medicamentos/métodos , Células Epiteliales/citología , Organoides , Técnicas de Cultivo de Célula/tendencias , Evaluación Preclínica de Medicamentos/tendencias , HumanosRESUMEN
Stem cells have significant potential use in tissue regeneration, especially for treating cardiac diseases because of their multi-directional differentiation capability. By mimicking the in vivo physiological environment of native cardiomyocytes during their development and maturation, researchers have been able to induce pluripotent stem cell-derived cardiomyocytes (PSC-CMs) at high purity. However, the phenotype of these PSC-CMs is immature compared with that of adult cardiomyocytes. Various strategies have been explored to improve the maturity of PSC-CMs, such as long-term culturing, mechanical stimuli, chemical stimuli, and combinations of these strategies. Among these strategies, mechanical stretch as a key mechanical stimulus plays an important role in PSC-CM maturation. In this review, the optimal parameters of mechanical stretch, the effects of mechanical stretch on maturation of PSC-CMs, underlying molecular mechanisms as well as existing problems are discussed. Mechanical stretch is a powerful approach to promote the maturation of SC-CMs in terms of morphology, structure, and functionality. Nonetheless, further research efforts are needed to reach a satisfactory standard for clinical applications of PSC-CMs in treating cardiac diseases.
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Diferenciación Celular/fisiología , Miocitos Cardíacos/fisiología , Células Madre Pluripotentes/fisiología , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Cardiopatías/terapia , Humanos , Miocitos Cardíacos/trasplante , Estrés MecánicoRESUMEN
In recent years, the development of 3D organoids has opened new avenues of investigation into development, physiology, and regenerative medicine. Organoid formation and the process of organogenesis share common developmental pathways; thus, our knowledge of developmental biology can help model the complexity of different organs to refine organoids into a more sophisticated platform. The developmental process is strongly dependent on complex networks and communication of cell-cell and cell-matrix interactions among different cell populations and their microenvironment, during embryogenesis. These interactions affect cell behaviors such as proliferation, survival, migration, and differentiation. Co-culture systems within the organoid technology were recently developed and provided the highly physiologically relevant systems. Supportive cells including various types of endothelial and stromal cells provide the proper microenvironment, facilitate organoid assembly, and improve vascularization and maturation of organoids. This review discusses the role of the co-culture systems in organoid generation, with a focus on how knowledge of developmental biology has directed and continues to shape the development of more evolved 3D co-culture system-derived organoids.
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Técnicas de Cultivo de Célula/métodos , Técnicas de Cocultivo/métodos , Organoides/crecimiento & desarrollo , Animales , Técnicas de Cultivo de Célula/tendencias , Diferenciación Celular , Técnicas de Cocultivo/tendencias , Biología Evolutiva/tendencias , Humanos , Organogénesis , Organoides/citología , Organoides/metabolismoRESUMEN
Mammalian cell culture has provided the foundation for the incredible expansion of cell biology to uncover the 'inner life of the cell'. The protocols for propagating cells in the laboratory have their origins in the mid-20th century. At that time the focus was on creating cell culture media that kept cells viable and favoured replicative growth. To the extent that oxygen level was considered as an important parameter, it was in the context of ensuring that oxygen was not depleted; the idea that environmental oxygen levels could be toxic was not widely appreciated. We increasingly understand that media composition and oxygen levels have important effects on cellular functions and that maintaining physiologically relevant conditions is necessary to maintain in vivo behaviours. We also understand much about the impact of growing cells that function in a 3D environment in 2D adherent monolayers. In this review, we examine some of the issues affecting standard cell culture approaches and new solutions that address these issues to increase the physiological accuracy of the cellular environment. We have reached a threshold in cell biology in which we know enough about the problems and their solutions to inform useful adjustments to protocols moving forward. This will increase the accuracy and translatability of this reductionist approach to understanding cell behaviours.
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Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Animales , Técnicas de Cultivo de Célula/historia , Historia del Siglo XX , Historia del Siglo XXIRESUMEN
Current in vitro models have played important roles in improving knowledge and understanding of cellular and molecular biology, but cannot exactly recapitulate the physiology of human tissues such as thyroid. In this article, we conducted a systematic review to present scientific and methodological time-trends of the reconstruction and generation of 3 D functional thyroid follicles and organoids for thyroid research in health and disease. "Web of Science (ISI)", "Scopus", "Embase", "Cochrane Library", and "PubMed" were systematically searched for papers published since 1950 to May 2020 in English language, using the predefined keywords. 212 articles were reviewed and finally 28 papers that met the inclusion and exclusion criteria were selected. Among the evidence for the examination of 3 D cell culture methods in thyroid research, there were only a few studies related to the organoid technology and its potential applications in understanding morphological, histological, and physiological characteristics of the thyroid gland and reconstructing this tissue. Besides, there was no study using organoids to investigate the tumorigenesis process of thyroid. Based on the results of this study, despite all the limitations and controversies, the exciting and promising organoid technology offers researchers a wide range of potential applications for more accurate modeling of thyroid in health and diseases and provides an excellent preclinical in vitro platform. In future, organoid technology can provide a better understanding of the molecular mechanisms of pathogenesis and tumorigenesis of thyroid tissue and more effective treatment for related disorders due to more accurate simulation of the thyroid physiology.
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Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Organoides/citología , Glándula Tiroides/citología , Técnicas de Cultivo de Célula/historia , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Modelos Biológicos , Medicina Regenerativa/historia , Medicina Regenerativa/métodos , Medicina Regenerativa/tendenciasRESUMEN
Monoclonal antibodies are widely used as diagnostic reagents and for therapeutic purposes, and their demand is increasing extensively. To produce these proteins in sufficient quantities for commercial use, it is necessary to raise the output by scaling up the production processes. This review describes recent trends in high-density cell culture systems established for monoclonal antibody production that are excellent methods to scale up from the lab-scale cell culture. Among the reactors, hollow fiber bioreactors contribute to a major part of high-density cell culture as they can provide a tremendous amount of surface area in a small volume for cell growth. As an alternative to hollow fiber reactors, a novel disposable bioreactor has been developed, which consists of a polymer-based supermacroporous material, cryogel, as a matrix for cell growth. Packed bed systems and disposable wave bioreactors have also been introduced for high cell density culture. These developments in high-density cell culture systems have led to the monoclonal antibody production in an economically favourable manner and made monoclonal antibodies one of the dominant therapeutic and diagnostic proteins in biopharmaceutical industry.
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Anticuerpos Monoclonales/biosíntesis , Reactores Biológicos , Biotecnología/métodos , Biotecnología/tendencias , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Animales , Formación de Anticuerpos , HumanosRESUMEN
It is of great value to develop reliable in vitro models for cell biology and toxicology. However, ethical issues and the decreasing number of donors restrict the further use of traditional animal models in various fields, including the emerging fields of tissue engineering and regenerative medicine. The huge gap created by the restrictions in animal models has pushed the development of the increasingly recognized three-dimensional (3D) cell culture, which enables cells to closely simulate authentic cellular behaviour such as close cell-to-cell interactions and can achieve higher functionality. Furthermore, 3D cell culturing is superior to the traditional 2D cell culture, which has obvious limitations and cannot closely mimic the structure and architecture of tissues. In this study, we review several methods used to form 3D multicellular spheroids. The extracellular microenvironment of 3D spheroids plays a role in many aspects of biological sciences, including cell signalling, cell growth, cancer cell generation, and anti-cancer drugs. More recently, they have been explored as basic construction units for tissue and organ engineering. We review this field with a focus on the previous research in different areas using spheroid models, emphasizing aqueous two-phase system (ATPS)-based techniques. Multi-cellular spheroids have great potential in the study of biological systems and can closely mimic the in vivo environment. New technologies to form and analyse spheroids such as the aqueous two-phase system and magnetic levitation are rapidly overcoming the technical limitations of spheroids and expanding their applications in tissue engineering and regenerative medicine.
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Ingeniería Biomédica/métodos , Técnicas de Cultivo de Célula/métodos , Dispositivos Laboratorio en un Chip , Esferoides Celulares/fisiología , Animales , Ingeniería Biomédica/tendencias , Técnicas de Cultivo de Célula/tendencias , Técnicas de Cocultivo , Humanos , Dispositivos Laboratorio en un Chip/tendencias , Preparaciones Farmacéuticas/administración & dosificación , Esferoides Celulares/efectos de los fármacosRESUMEN
Three-dimensional cell culture technology is a novel cell culture technology, which can simulate the growth state of cells in vivo by scaffolds or special devices. Cells can form tissues or organs in vitro. It combines some advantages of traditional cell experiments and animal model experiments. Because of its advantages, it is widely used in clinical medical research, including research on stem cell differentiation, research on cell behavior, migration and invasion, study on microenvironment, study on drug sensitivity and radio-sensitivity of tumor cells, etc. In this paper, the evolution and classification of three-dimensional cell culture are reviewed, also the advantages and shortages are compared. The application of three-dimensional cell culture in clinical medicine are summarized to provide an insight into translational medicine.
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Técnicas de Cultivo de Célula/instrumentación , Investigación Biomédica Traslacional/métodos , Animales , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , HumanosRESUMEN
In vitro cell cultures are crucial research tools for modeling human development and diseases. Although the conventional monolayer cell cultures have been widely used in the past, the lack of tissue architecture and complexity of such model fails to inform the true biological processes in vivo. Recent advances in the organoid technology have revolutionized the in vitro culture tools for biomedical research by creating powerful three-dimensional (3D) models to recapitulate the cellular heterogeneity, structure, and functions of the primary tissues. Such organoid technology enables researchers to recreate human organs and diseases in a dish and thus holds great promises for many translational applications such as regenerative medicine, drug discovery, and precision medicine. In this review, we provide an overview of the organoid history and development. We discuss the strengths and limitations of organoids as well as their potential applications in the laboratory and the clinic.
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Investigación Biomédica/métodos , Técnicas de Cultivo de Célula/métodos , Modelos Biológicos , Organoides/fisiología , Animales , Investigación Biomédica/tendencias , Técnicas de Cultivo de Célula/tendencias , Humanos , Técnicas de Cultivo de Órganos/métodos , Técnicas de Cultivo de Órganos/tendencias , Organoides/citologíaRESUMEN
BACKGROUND: Understanding the molecular and cellular mechanisms of human reproductive development has been limited by the scarcity of human samples and ethical constraints. Recently, in vitro differentiation of human pluripotent stem cells into germ cells and single-cell analyses have opened new avenues to directly study human germ cells and identify unique mechanisms in human reproductive development. OBJECTIVE AND RATIONALE: The goal of this review is to collate novel findings and insightful discoveries with these new methodologies, aiming at introducing researchers and clinicians to the use of these tools to study human reproductive biology and develop treatments for infertility. SEARCH METHODS: PubMed was used to search articles and reviews with the following main keywords: in vitro differentiation, human stem cells, single-cell analysis, spermatogenesis, oogenesis, germ cells and other key terms related to these subjects. The search period included all publications from 2000 until now. OUTCOMES: Single-cell analyses of human gonads have identified many important gene markers at different developmental stages and in subpopulations of cells. To validate the functional roles of these gene markers, researchers have used the in vitro differentiation of human pluripotent cells into germ cells and confirmed that some genetic requirements are unique in human germ cells and are not conserved in mouse models. Moreover, transcriptional regulatory networks and the interaction of germ and somatic cells in gonads were elucidated in these studies. WIDER IMPLICATIONS: Single-cell analyses allow researchers to identify gene markers and potential regulatory networks using limited clinical samples. On the other hand, in vitro differentiation methods provide clinical researchers with tools to examine these newly identify gene markers and study the causative effects of mutations previously associated with infertility. Combining these two methodologies, researchers can identify gene markers and networks which are essential and unique in human reproductive development, thereby producing more accurate diagnostic tools for assessing reproductive disorders and developing treatments for infertility.
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Técnicas de Cultivo de Célula/tendencias , Diferenciación Celular/fisiología , Células Germinativas/fisiología , Células Madre Pluripotentes/fisiología , Reproducción/fisiología , Medicina Reproductiva/tendencias , Análisis de la Célula Individual , Animales , Técnicas de Cultivo de Célula/métodos , Células Cultivadas , Femenino , Células Germinativas/citología , Humanos , Masculino , Ratones , Oogénesis/fisiología , Células Madre Pluripotentes/citología , Medicina Reproductiva/métodos , Análisis de la Célula Individual/métodos , Análisis de la Célula Individual/tendencias , Espermatogénesis/fisiologíaRESUMEN
As burden of chronic respiratory diseases is constantly increasing, improving in vitro lung models is essential in order to reproduce as closely as possible the complex pulmonary architecture, responsible for oxygen uptake and carbon dioxide clearance. The study of diseases that affect the respiratory system has benefited from in vitro reconstructions of the respiratory epithelium with inserts in air/liquid interface (2D) or in organoids able to mimic up to the arborescence of the respiratory tree (3D). Recent development in the fields of pluripotent stem cells-derived organoids and genome editing technologies has provided new insights to better understand pulmonary diseases and to find new therapeutic perspectives.
TITLE: Les organoïdes pulmonaires. ABSTRACT: L'impact en santé publique des pathologies respiratoires chroniques ne cesse de croître. Dans ce contexte, il paraît indispensable d'améliorer les modèles d'études du poumon afin de reproduire au plus proche l'architecture pulmonaire complexe, garante des fonctions d'oxygénation et d'épuration du gaz carbonique. Les connaissances actuelles en physiopathologie respiratoire résultent en partie des études de modèles de reconstitution d'épithélium bronchique in vitro à partir de cellules primaires, en deux dimensions sur des inserts, ou en trois dimensions, en organoïdes mimant jusqu'à l'arborescence pulmonaire. Le développement de ces modèles in vitro a connu un nouvel essor grâce aux organoïdes pulmonaires issus de cellules souches pluripotentes et la démocratisation des outils d'édition du génome. Ces apports technologiques récents offrent de nouvelles perspectives en matière de thérapeutiques ou de compréhension physiopathologique et pourraient, dans le futur, ouvrir les portes de la médecine régénératrice pulmonaire.
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Técnicas de Cultivo de Célula , Pulmón/citología , Organoides/citología , Células Epiteliales Alveolares/citología , Células Epiteliales Alveolares/fisiología , Animales , Bioingeniería/métodos , Bioingeniería/tendencias , Dióxido de Carbono/farmacología , Dióxido de Carbono/fisiología , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Células Cultivadas , Edición Génica/métodos , Edición Génica/tendencias , Humanos , Pulmón/patología , Pulmón/fisiología , Modelos Biológicos , Organoides/patología , Organoides/fisiología , Oxígeno/farmacología , Oxígeno/fisiología , Intercambio Gaseoso Pulmonar/fisiología , Mucosa Respiratoria/citología , Mucosa Respiratoria/efectos de los fármacos , Andamios del Tejido/químicaAsunto(s)
Técnicas de Cultivo de Célula , Organoides/citología , Animales , Bioingeniería/ética , Bioingeniería/métodos , Bioingeniería/tendencias , Técnicas de Cultivo de Célula/ética , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Células Cultivadas , Experimentación Humana/ética , Humanos , Células Madre Pluripotentes Inducidas/citología , Células Madre Pluripotentes Inducidas/fisiología , Organoides/patología , Obtención de Tejidos y Órganos/ética , Obtención de Tejidos y Órganos/métodos , Obtención de Tejidos y Órganos/tendenciasRESUMEN
High-throughput in vitro models lack human-relevant complexity, which undermines their ability to accurately mimic in vivo biologic and pathologic responses. The emergence of microphysiological systems (MPS) presents an opportunity to revolutionize in vitro modeling for both basic biomedical research and applied drug discovery. The MPS platform has been an area of interdisciplinary collaboration to develop new, predictive, and reliable in vitro methods for regulatory acceptance. The current MPS models have been developed to recapitulate an organ or tissue on a smaller scale. However, the complexity of these models (ie, including all cell types present in the in vivo tissue) with appropriate structural, functional, and biochemical attributes are often not fully characterized. Here, we provide an overview of the capabilities and limitations of the microfluidic MPS model (aka organs-on-chips) within the scope of drug development. We recommend the engagement of pathologists early in the MPS design, characterization, and validation phases, because this will enable development of more robust and comprehensive MPS models that can accurately replicate normal biology and pathophysiology and hence be more predictive of human responses.
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Técnicas In Vitro/métodos , Modelos Biológicos , Animales , Biomarcadores , Técnicas de Cultivo de Célula/métodos , Técnicas de Cultivo de Célula/tendencias , Enfermedades Transmisibles , Descubrimiento de Drogas/métodos , Neoplasias , Patólogos , Células Madre Pluripotentes , Técnicas de Cultivo de Tejidos/métodos , Técnicas de Cultivo de Tejidos/tendenciasRESUMEN
Temperature shifts to lower culture temperatures are frequently employed in the manufacturing of protein therapeutics in mammalian cells to improve productivity, viability, or quality attributes. The direction and extent to which a temperature shift affects productivity and quality may vary depending on the expression host and characteristics of the expressed protein. We demonstrated here that two Chinese hamster ovary (CHO) clones expressing different human monoclonal antibodies responded differently to a temperature shift despite sharing a common parental CHO cell line. Within a single CHO line, we observed a nonlinear response to temperature shift. A moderate shift to 35°C significantly decreased final titer relative to the unshifted control while a larger shift to 32°C significantly increased final titer by 25%. Therefore, we proposed a systematic empirical approach to assess the utility of a temperature shift for faster implementation during process development. By testing multiple shift parameters, we identified optimum shift conditions in shake flasks and successfully translated findings to benchtop bioreactors and 1,000-L bioreactor scale. Significant differences in final antibody titer and charge variants were observed with temperature shift increments as small as Δ1.5°C. Acidic charge variants decreased monotonically with decreasing shift temperature in both cell lines; however, final antibody titer required simultaneous optimization of shift day and temperature. Overall, we were able to show that a systematic approach to identify temperature shift parameters at small scales is useful to optimize protein production and quality for efficient and confident translation to large-scale production.
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Anticuerpos Monoclonales/biosíntesis , Reactores Biológicos , Células CHO , Técnicas de Cultivo de Célula/tendencias , Animales , Anticuerpos Monoclonales/genética , Cricetinae , Cricetulus , Humanos , TemperaturaRESUMEN
Microcarriers are 100- to 300-micron support matrices that permit the growth of adherent cells in bioreactor systems. They have a larger surface area to volume ratio in comparison to single cell monolayers, enabling cost-effective cell production and expansion. Microcarriers are composed of a solid matrix that must be separated from expanded cells during downstream processing stages. The detachment method is chosen on the basis of several factors like cell type, microcarrier surface chemistry, cell confluency and degree of aggregation. The development of microcarriers with a range of physiochemical properties permit controlled cell and protein associations that hold utility for novel therapeutics. In this review, we provide an overview of the recent advances in microcarrier cell culture technology. We also discuss its significance as an ex vivo research tool and the therapeutic potential of newly designed microcarrier systems in vivo.
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Biotecnología/métodos , Técnicas de Cultivo de Célula/métodos , Microesferas , Reactores Biológicos , Biotecnología/tendencias , Técnicas de Cultivo de Célula/tendenciasRESUMEN
The past decade has witnessed remarkable development in tissue engineering technologies and stem cells. Our lab has developed a novel technology - "cell sheet technology" for tissue engineering. After the confluent cells are cultured on an innovative temperature-responsive culture dish, the cells can be harvested as an intact sheet by lowering temperature. We have successfully created multiple cell sheet-based tissues for therapies of a vast variety of diseases, in particular, myocardial diseases. On the other side, the discovery of human induced pluripotent stem cells (hiPSC) enables stable production of defined tissue-specific cell types and thus makes it possible to regenerate tissues or even organs for clinical application and in vitro drug screening/disease modeling. Recently, we have combined cell sheet technology and hiPSC-derived cardiac cells for fabrication of functional human cardiac tissues. This review summarizes ongoing challenges in this field and our progresses in solving issues, such as large scale culture of hiPSC-derived cardiac cells, elimination of undifferentiated iPSCs to decrease the risk of tumor formation as well as myocardial tissue fabrication technologies.
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Cardiomiopatías/terapia , Técnicas de Cultivo de Célula/tendencias , Células Madre Pluripotentes Inducidas/fisiología , Miocitos Cardíacos/trasplante , Ingeniería de Tejidos/tendencias , Técnicas de Cultivo de Célula/métodos , Diferenciación Celular , Humanos , Miocitos Cardíacos/fisiología , Ingeniería de Tejidos/métodosRESUMEN
The use of GM animals to produce human recombinant therapeutic proteins has progressed only slowly. But recent successes and new technologies could speed up development.