ABSTRACT
Transgenerational epigenetic inheritance in mammals remains a debated subject. Here, we demonstrate that DNA methylation of promoter-associated CpG islands (CGIs) can be transmitted from parents to their offspring in mice. We generated DNA methylation-edited mouse embryonic stem cells (ESCs), in which CGIs of two metabolism-related genes, the Ankyrin repeat domain 26 and the low-density lipoprotein receptor, were specifically methylated and silenced. DNA methylation-edited mice generated by microinjection of the methylated ESCs exhibited abnormal metabolic phenotypes. Acquired methylation of the targeted CGI and the phenotypic traits were maintained and transmitted across multiple generations. The heritable CGI methylation was subjected to reprogramming in parental PGCs and subsequently reestablished in the next generation at post-implantation stages. These observations provide a concrete step toward demonstrating transgenerational epigenetic inheritance in mammals, which may have implications in our understanding of evolutionary biology as well as the etiology, diagnosis, and prevention of non-genetically inherited human diseases.
Subject(s)
DNA Methylation , Epigenesis, Genetic , Mice , Humans , Animals , CpG Islands , Inheritance Patterns , Mammals/geneticsABSTRACT
Interspecies blastocyst complementation enables organ-specific enrichment of xenogenic pluripotent stem cell (PSC) derivatives. Here, we establish a versatile blastocyst complementation platform based on CRISPR-Cas9-mediated zygote genome editing and show enrichment of rat PSC-derivatives in several tissues of gene-edited organogenesis-disabled mice. Besides gaining insights into species evolution, embryogenesis, and human disease, interspecies blastocyst complementation might allow human organ generation in animals whose organ size, anatomy, and physiology are closer to humans. To date, however, whether human PSCs (hPSCs) can contribute to chimera formation in non-rodent species remains unknown. We systematically evaluate the chimeric competency of several types of hPSCs using a more diversified clade of mammals, the ungulates. We find that naïve hPSCs robustly engraft in both pig and cattle pre-implantation blastocysts but show limited contribution to post-implantation pig embryos. Instead, an intermediate hPSC type exhibits higher degree of chimerism and is able to generate differentiated progenies in post-implantation pig embryos.
Subject(s)
Chimerism , Gene Editing , Mammals/embryology , Animals , Blastocyst , CRISPR-Cas Systems , Cattle , Embryo, Mammalian/cytology , Female , Humans , Male , Mammals/classification , Mice , Mice, Inbred C57BL , Mice, Inbred ICR , Pluripotent Stem Cells , Rats , Rats, Sprague-Dawley , Sus scrofaABSTRACT
Diferentes enfermedades afectan la tráquea y deterioran la calidad de vida. La ingeniería tisular es una alternativa terapéutica para los pacientes con esas enfermedades: matrices de tráquea descelularizadas y sembradas con células del receptor no generan respuesta inmune y pueden prevenir incluso el rechazo de zootrasplantes. Objetivo: evaluar un método de descelularización para obtener matrices extracelulares de tráquea en el modelo porcino. Materiales y métodos: a partir de 5 tráqueas porcinas se formaron dos grupos de estudio, controles y tratados con un método químico-enzimático. Se hizo análisis histológico con hematoxilina-eosina, coloración tricrómica de Masson y safranina O. Se evaluaron las propiedades biomecánicas de ambos grupos, mediante la determinación del módulo de Young, la fuerza máxima y el porcentaje de deformación. Resultados: en las muestras tratadas se observó una disminución del 66 % del contenido celular en comparación con los controles. Se preservó el colágeno y se detectó reducción de los glucosaminoglucanos. Las pruebas biomecánicas revelaron una diferencia estadísticamente significativa del porcentaje de deformación, sin alteración de los demás parámetros. Conclusiones: el método evaluado demostró ser eficiente para descelularizar tráqueas de cerdo, con una disminución importante en el costo y el tiempo de tratamiento, por lo que podría ser una buena opción en las condiciones socioeconómicas de Colombia...
Different diseases may affect the trachea and, therefore, the quality of life. Tissue engineering may be a therapeutic alternative for patientswith such diseases, using decellularized trachea matrixes seeded with cells from the recipient, which do not generate immune response and may even prevent rejection of zoo-transplants. Objective: To evaluate a decellularization method to obtain tracheal extracellular matrixes in the porcine model. Materials and methods: Two study groups, treated and control, were obtained from 5 porcine tracheas.A chemical-enzymatic method for decellularization was used. Histological analyses were performed with hematoxylin-eosin, Massons trichromic stain and safranin O. Biomechanical properties of both groups were evaluated by determining the Young modulus, maximum strength and deformation rate. Results: Compared to the controls, there was a 66 % decrease in the cell content in the treated specimens. Collagen was preserved and a reduction of glycosaminoglycans was detected. Biomechanical tests revealed a significant difference in the percentage of deformation, with no alteration of the remaining parameters. Conclusions: The evaluated decellularization method proved to be efficient to reduce the cellular content of porcine tracheas, with a considerable decrease in cost and production time. These advantages could make it a good option for the socio-economic Colombian conditions...
Diferentes doenças afetam a traqueia e deterioram a qualidade de vida. A engenheira tisular é uma alternativa terapêutica para os pacientes com essas doenças: matrizes de traqueia descelularizadas e semeadas com células do receptor não geram resposta imune e podem prevenir incluso a rejeição de zoo-transplantes. Objetivo: avaliar um método de descelularização para obter matrizes extracelulares de traqueia no modelo suíno. Materiais e métodos: a partir de 5 traqueias suínas se formaram dois grupos de estudo, controles e tratados com um método químico-enzimático. Se fez análise histológico com hematoxilina-eosina, corante tricrómica de Masson e safranina O. Se avaliaram as propriedades biomecânicas de ambos grupos, mediante a determinação do módulo de Young, a força máxima e a porcentagem de deformação. Resultados: Nas amostras tratadas se observou uma diminuição de 66 % do conteúdo celular em comparação com os controles. Se preservou o colágenoe se detectou redução dos glucosaminoglucanos. As provas biomecânicas revelaram uma diferença estatisticamente significativa da porcentagem de deformação, sem alteração dos demais parâmetros. Conclusões: O método avaliado demostrou ser eficiente para descelularizar traqueias de porco, com uma diminuição importante no custo e o tempo de tratamento, pelo que poderia ser uma boa opção nas condições socioeconómicas da Colômbia...