RESUMEN
We generated and characterized a rhesus macaque induced pluripotent stem cell (iPSC) line using induced reprogramming of fibroblasts isolated from a rhesus macaque fetus. The fibroblasts were expanded and then reprogrammed using non-integrating Sendai virus technology. This line is available as riPSC05. The authenticity of riPSC05 was confirmed through the expression of pluripotent and self-renewal markers, in vitro-directed differentiation towards three germ layers (ectoderm, mesoderm, and endoderm), karyotyping, and STR analysis.
Asunto(s)
Células Madre Pluripotentes Inducidas , Animales , Células Madre Pluripotentes Inducidas/metabolismo , Reprogramación Celular , Macaca mulatta , Diferenciación Celular , Cariotipificación , Fibroblastos/metabolismoRESUMEN
Three-dimensional (3D) stem cell models of the ovary have the potential to benefit women's reproductive health research. One such model, the reconstituted ovary (rOvary) self-assembles with pluripotent stem cell-derived germ cells creating a 3D ovarian mimic competent to support the differentiation of functional oocytes inside follicles. In this study, we evaluated the cellular composition of the rOvary revealing the capacity to generate multiple follicles surrounded by NR2F2+ stroma cells. However, the rOvary does not develop a surface epithelium, the source of second-wave pre-granulosa cells, or steroidogenic theca. Therefore, the rOvary models represent the self-assembly of activated follicles in a pre-pubertal ovary poised but not yet competent for hormone production.
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Folículo Ovárico , Ovario , Femenino , Humanos , Ovario/metabolismo , Oocitos , Células de la Granulosa/metabolismo , EpitelioRESUMEN
OBJECTIVE: There is room for improvement in the knowledge of female gout, often noted at risk of gender blindness. This study aims to compare the prevalence of comorbidities in women versus men hospitalised with gout in Spain. METHODS: This is an observational, multicentre, cross-sectional study in public and private Spanish hospitals analysing the minimum basic data set from 192 037 hospitalisations in people with gout (International Classification of Diseases, Ninth Revision (ICD-9) coding) from 2005 to 2015. Age and several comorbidities (ICD-9) were compared by sex, with a subsequent stratification of comorbidities by age group. The association between each comorbidity and sex was assessed using multivariable logistic regression. A clinical decision tree algorithm was constructed to predict the sex of patients with gout based on age and comorbidities alone. RESULTS: Women with gout (17.4% of the sample) were significantly older than men (73.9±13.7 years vs 64.0±14.4 years, p<0.001). Obesity, dyslipidaemia, chronic kidney disease, diabetes mellitus, heart failure, dementia, urinary tract infection and concurrent rheumatic disease were more common in women. Female sex was strongly associated with increasing age, heart failure, obesity, urinary tract infection and diabetes mellitus, while male sex was associated with obstructive respiratory diseases, coronary disease and peripheral vascular disease. The decision tree algorithm built showed an accuracy of 74.4%. CONCLUSIONS: A nationwide analysis of inpatients with gout in 2005-2015 confirms a different comorbidity profile between men and women. A different approach to female gout is needed to reduce gender blindness.
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Diabetes Mellitus , Gota , Insuficiencia Cardíaca , Masculino , Humanos , Femenino , Estudios Transversales , Gota/epidemiología , Comorbilidad , Diabetes Mellitus/epidemiología , Obesidad/epidemiología , Insuficiencia Cardíaca/epidemiologíaRESUMEN
The "Espinar" stabilization lagoon is a body of wastewater that is located in the district (region of Puno), which accumulates wastewater that comes from the population of the city of Puno-Peru. The present study was carried out in January and February of 2019 in affluent and effluent wastewater. The measures of pH, water temperature, total suspended solids, electrical conductivity and salinity were evaluated. The results showed that there are significant differences between the data of the affluent and effluent samples during the periods analyzed (Krustal Wallis). The median concentrations values of the effluent for the parameters of temperature (16.60 °C), salinity (0.67 mg/L), pH (7.70), total dissolved solids (669.00 ppm) and electrical conductivity (1463.07 µs/cm), they all show significant differences. Also, the removal efficiency was calculated by the total dissolved solids (TDS) and the positive removal of 7.80% of pollutant load was found. Although these results are within the established limits, the monitoring mechanisms must be established for an adequate control of the parameters evaluated and thus, there won't be a deterioration of the environment surrounding the lagoon.
RESUMEN
Six human induced pluripotent stem cell sublines (hiPSCs) were generated from human dermal fibroblasts (HDFs) derived from skin biopsies donated from monozygotic twin women wherein one woman had proven fertility and her sister was infertile due to ovarian failure. Three hiPSC sublines were created from each twin's HDFs. hiPSCs were reprogrammed using Sendai virus vectors and were subsequently positive for markers of self-renewal including OCT4, NANOG, TRA-1-81 and SSEA-4. Pluripotency was further verified using PluriTest. We show here that the hiPSC lines created from the twins are equivalent in measures of pluripotency and self-renewal, despite their differential diagnosis.
Asunto(s)
Células Madre Pluripotentes Inducidas , Diferenciación Celular , Reprogramación Celular , Femenino , Fibroblastos , Humanos , Virus Sendai , PielRESUMEN
Human testis development in prenatal life involves complex changes in germline and somatic cell identity. To better understand, we profiled and analyzed â¼32,500 single-cell transcriptomes of testicular cells from embryonic, fetal, and infant stages. Our data show that at 6-7 weeks postfertilization, as the testicular cords are established, the Sertoli and interstitial cells originate from a common heterogeneous progenitor pool, which then resolves into fetal Sertoli cells (expressing tube-forming genes) or interstitial cells (including Leydig-lineage cells expressing steroidogenesis genes). Almost 10 weeks later, beginning at 14-16 weeks postfertilization, the male primordial germ cells exit mitosis, downregulate pluripotent transcription factors, and transition into cells that strongly resemble the state 0 spermatogonia originally defined in the infant and adult testes. Therefore, we called these fetal spermatogonia "state f0." Overall, we reveal multiple insights into the coordinated and temporal development of the embryonic, fetal, and postnatal male germline together with the somatic niche.
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Células de Sertoli , Testículo , Adulto , Femenino , Humanos , Masculino , Embarazo , Análisis de la Célula Individual , Espermatogonias , Células MadreRESUMEN
The development of an in vitro system in which human primordial germ cell-like cells (hPGCLCs) are generated from human pluripotent stem cells (hPSCs) has been invaluable to further our understanding of human primordial germ cell (hPGC) specification. However, the means to evaluate the next fundamental steps in germ cell development have not been well established. In this study we describe a two dimensional extended culture system that promotes proliferation of specified hPGCLCs, without reversion to a pluripotent state. We demonstrate that hPGCLCs in extended culture undergo partial epigenetic reprogramming, mirroring events described in hPGCs in vivo, including a genome-wide reduction in DNA methylation and maintenance of depleted H3K9me2. This extended culture system provides a new approach for expanding the number of hPGCLCs for downstream technologies, including transplantation, molecular screening, or possibly the differentiation of hPGCLCs into gametes by in vitro gametogenesis.
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Técnicas de Cultivo de Célula/métodos , Metilación de ADN , Células Germinativas/citología , Proliferación Celular , Autorrenovación de las Células , Supervivencia Celular , Células Cultivadas , Ensamble y Desensamble de Cromatina , Desmetilación del ADN , Metilación de ADN/genética , Histonas/metabolismo , Humanos , Transcripción Genética , Transcriptoma/genéticaRESUMEN
We generated three human induced pluripotent stem cell (hiPSC) sublines from human dermal fibroblasts (HDFs) (MZT04) generated from a skin biopsy donated from a previously fertile woman. The skin biopsy was broadly consented for generating hiPSC lines for biomedical research, including unique consent specifically for studying human fertility, infertility and germ cells. hiPSCs were reprogrammed using Sendai virus vectors and were subsequently positive for markers of self-renewal including OCT4, NANOG, TRA-1-81 and SSEA-4. Pluripotency was further verified using teratomas and PluriTest. These sublines serve as controls for hiPSC research projects aimed at understanding the cell and molecular regulation of female fertility and infertility.
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Línea Celular/citología , Células Madre Pluripotentes Inducidas/citología , Diferenciación Celular , Línea Celular/metabolismo , Células Cultivadas , Reprogramación Celular , Femenino , Fibroblastos/citología , Fibroblastos/metabolismo , Homocigoto , Humanos , Células Madre Pluripotentes Inducidas/metabolismo , Masculino , Persona de Mediana Edad , Factor 3 de Transcripción de Unión a Octámeros/genética , Factor 3 de Transcripción de Unión a Octámeros/metabolismo , Factores de Transcripción SOXB1/genética , Factores de Transcripción SOXB1/metabolismoRESUMEN
A major challenge in stem cell differentiation is the availability of bioassays to prove cell types generated in vitro are equivalent to cells in vivo. In the mouse, differentiation of primordial germ cell-like cells (PGCLCs) from pluripotent cells was validated by transplantation, leading to the generation of spermatogenesis and to the birth of offspring. Here we report the use of xenotransplantation (monkey to mouse) and homologous transplantation (monkey to monkey) to validate our in vitro protocol for differentiating male rhesus (r) macaque PGCLCs (rPGCLCs) from induced pluripotent stem cells (riPSCs). Specifically, transplantation of aggregates containing rPGCLCs into mouse and nonhuman primate testicles overcomes a major bottleneck in rPGCLC differentiation. These findings suggest that immature rPGCLCs once transplanted into an adult gonadal niche commit to differentiate towards late rPGCs that initiate epigenetic reprogramming but do not complete the conversion into ENO2-positive spermatogonia.
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Células Madre Pluripotentes Inducidas/citología , Células Madre Pluripotentes Inducidas/trasplante , Espermatocitos/citología , Espermatogénesis/fisiología , Espermatogonias/citología , Testículo/metabolismo , Animales , Células Cultivadas , Femenino , Humanos , Macaca mulatta , Masculino , Ratones , Ratones Desnudos , Proteínas de Neoplasias/metabolismo , Fosfopiruvato Hidratasa/metabolismo , Trasplante Heterólogo , Trasplante HomólogoRESUMEN
Cellular replacement therapies for neurological conditions use human embryonic stem cell (hESC)- or induced pluripotent stem cell (hiPSC)-derived neurons to replace damaged or diseased populations of neurons. For the spinal cord, significant progress has been made generating the in-vitro-derived motor neurons required to restore coordinated movement. However, there is as yet no protocol to generate in-vitro-derived sensory interneurons (INs), which permit perception of the environment. Here, we report on the development of a directed differentiation protocol to derive sensory INs for both hESCs and hiPSCs. Two developmentally relevant factors, retinoic acid in combination with bone morphogenetic protein 4, can be used to generate three classes of sensory INs: the proprioceptive dI1s, the dI2s, and mechanosensory dI3s. Critical to this protocol is the competence state of the neural progenitors, which changes over time. This protocol will facilitate developing cellular replacement therapies to reestablish sensory connections in injured patients.
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Células Madre Embrionarias Humanas/citología , Células Madre Pluripotentes Inducidas/trasplante , Células Receptoras Sensoriales/citología , Médula Espinal/crecimiento & desarrollo , Proteína Morfogenética Ósea 4/farmacología , Técnicas de Cultivo de Célula , Diferenciación Celular/efectos de los fármacos , Diferenciación Celular/genética , Células Madre Embrionarias Humanas/trasplante , Humanos , Células Madre Pluripotentes Inducidas/citología , Interneuronas/citología , Interneuronas/trasplante , Células Receptoras Sensoriales/trasplante , Médula Espinal/fisiopatología , Médula Espinal/trasplante , Tretinoina/farmacologíaRESUMEN
The rhesus macaque induced pluripotent stem cell (riPSC) line, UCLAi090-A (riPSC90), was generated from rhesus embryonic fibroblast (REF) cells called REF90. REF90 cells and the riPSC90 line were authenticated by short tandem repeat analysis and had a normal male (42, XY) karyotype. The riPSC90 line expressed markers of self-renewal including OCT4, NANOG, TRA-1-81 and SSEA4, and generated teratomas after transplantation into immunocompromised mice. riPSC90 could be used in parallel with riPSC89, which was derived from REFs cultured from a different rhesus macaque embryo (Sosa et al. 2016).
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Embrión de Mamíferos/metabolismo , Técnicas de Transferencia de Gen , Células Madre Pluripotentes Inducidas/metabolismo , Factores de Transcripción , Animales , Línea Celular , Embrión de Mamíferos/citología , Células Madre Pluripotentes Inducidas/citología , Macaca mulatta , Masculino , Ratones , Ratones SCID , Factores de Transcripción/biosíntesis , Factores de Transcripción/genéticaRESUMEN
Primordial germ cells (PGCs) are the earliest embryonic progenitors in the germline. Correct formation of PGCs is critical to reproductive health as an adult. Recent work has shown that primate PGCs can be differentiated from pluripotent stem cells; however, a bioassay that supports their identity as transplantable germ cells has not been reported. Here, we adopted a xenotransplantation assay by transplanting single-cell suspensions of human and nonhuman primate embryonic Macaca mulatta (rhesus macaque) testes containing PGCs into the seminiferous tubules of adult busulfan-treated nude mice. We discovered that both human and nonhuman primate embryonic testis are xenotransplantable, generating colonies while not generating tumors. Taken together, this work provides two critical references (molecular and functional) for defining transplantable primate PGCs. These results provide a blueprint for differentiating pluripotent stem cells to transplantable PGC-like cells in a species that is amenable to transplantation and fertility studies.
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Células Germinativas/trasplante , Túbulos Seminíferos/cirugía , Testículo/embriología , Testículo/trasplante , Animales , Busulfano/uso terapéutico , Femenino , Humanos , Inmunosupresores/uso terapéutico , Macaca mulatta , Masculino , Ratones Desnudos , Trasplante Heterólogo/métodosRESUMEN
Human fertility is dependent upon the correct establishment and differentiation of the germline. This is because no other cell type in the body is capable of passing a genome and epigenome from parent to child. Terminally differentiated germline cells in the adult testis and ovary are called gametes. However, the initial specification of germline cells occurs in the embryo around the time of gastrulation. Most of our knowledge regarding the cell and molecular events that govern human germline specification involves extrapolating scientific principles from model organisms, most notably the mouse. However, recent work using next generation sequencing, gene editing and differentiation of germline cells from pluripotent stem cells has revealed that the core molecular mechanisms that regulate human germline development are different from rodents. Here, we will discuss the major molecular pathways required for human germline differentiation and how pluripotent stem cells have revolutionized our ability to study the earliest steps in human embryonic lineage specification in order to understand human fertility.
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Infertilidad/patología , Modelos Biológicos , Células Madre Pluripotentes/patología , Linaje de la Célula , Células Germinativas/citología , Humanos , Reproducción/fisiologíaRESUMEN
We generated a rhesus macaque induced pluripotent stem cell (riPSC) line, riPSC89, from rhesus embryonic fibroblasts (REFs). Fibroblasts were expanded from the skin of a rhesus macaque embryo at embryonic day 47. REFs and riPSCs had a normal male (42, XY) karyotype. The riPSC89 line was positive for markers of self-renewal including OCT4, NANOG, TRA-1-81 and SSEA4. Pluripotency was demonstrated through the generation of teratomas using transplantation into immunocompromised mice. The riPSC89 line may be a useful non-human primate resource to uncover developmental origins of disease, or used as a basic model to understand lineage specification in the primate embryo.
Asunto(s)
Reprogramación Celular , Embrión de Mamíferos/citología , Fibroblastos/citología , Células Madre Pluripotentes Inducidas/metabolismo , Animales , Línea Celular , Fibroblastos/metabolismo , Células Madre Pluripotentes Inducidas/citología , Células Madre Pluripotentes Inducidas/trasplante , Cariotipo , Macaca mulatta , Masculino , Ratones , Ratones Endogámicos NOD , Teratoma/metabolismo , Teratoma/patología , Factores de Transcripción/genética , Factores de Transcripción/metabolismoRESUMEN
Past studies have indicated that transcription of all X-linked genes is repressed by meiotic sex chromosome inactivation (MSCI) during the meiotic phase of spermatogenesis in mammals. However, more recent studies have shown an increase in steady-state levels of certain X-linked miRNAs in pachytene spermatocytes, suggesting that either synthesis of these miRNAs increases or that degradation of these miRNAs decreases dramatically in these cells. To distinguish between these possibilities, we performed RNA-FISH to detect nascent transcripts from multiple miRNA genes in various spermatogenic cell types. Our results show definitively that Type I X-linked miRNA genes are subject to MSCI, as are all or most X-linked mRNA genes, whereas Type II and III X-linked miRNA genes escape MSCI by continuing ongoing, active transcription in primary spermatocytes. We corroborated these results by co-localization of RNA-FISH signals with both a corresponding DNA-FISH signal and an immunofluorescence signal for RNA polymerase II. We also found that X-linked miRNA genes that escape MSCI locate non-randomly to the periphery of the XY body, whereas genes that are subject to MSCI remain located within the XY body in pachytene spermatocytes, suggesting that the mechanism of escape of X-linked miRNA genes from MSCI involves their relocation to a position outside of the repressive chromatin domain associated with the XY body. The fact that Type II and III X-linked miRNA genes escape MSCI suggests an immediacy of function of the encoded miRNAs specifically required during the meiotic stages of spermatogenesis.
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Ratones/metabolismo , Espermatogénesis , Inactivación del Cromosoma X , Animales , Cromosomas de los Mamíferos , Hibridación Fluorescente in Situ , Masculino , Meiosis , Ratones/genética , MicroARNs , Espermatocitos/metabolismo , Testículo/citología , Testículo/metabolismo , Transcripción Genética , Cromosoma X/metabolismo , Cromosoma Y/metabolismoRESUMEN
El consumo de drogas psicotrópicas es uno de los grandes problemas de salud en el mundo. La cocaína, en sus distintas presentaciones y vías de administración tales como la aplicación por frotación sobre la encía, se convirtió en especial interés para esta investigación, debido a que en nuestra actividad clínica hemos encontrado casos aislados de alteraciones periodontales en las cuales los pacientes aseguraron haber usado cocaína por frotación sobre la zona afectada. En este estudio se utilizaron 40 ratas de la cepa Wistar (20 experimentales y 20 control) durante 16 semanas. Se demostró que la cocaína produce alteraciones clínicas e histológicas en la encía, siendo la gingivitis crónica la patología más frecuente en un 70 por ciento de los casos, por lo cual se debe considerar en la evaluación clínica el consumo de drogas como factor de riesgo de la enfermedad periodontal
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Animales , Ratas , Cocaína/efectos adversos , Periodoncio , Trastornos Relacionados con Cocaína/complicaciones , Trastornos Relacionados con Cocaína/diagnóstico , Encía/ultraestructura , Gingivitis , Periodoncio , Ratas Wistar , Interpretación Estadística de DatosRESUMEN
El consumo de drogas psicotrópicas es uno de los grandes problemas de salud en el mundo. La cocaína, en sus distintas presentaciones y vías de administración tales como la aplicación por frotación sobre la encía, se convirtió en especial interés para esta investigación, debido a que en nuestra actividad clínica hemos encontrado casos aislados de alteraciones periodontales en las cuales los pacientes aseguraron haber usado cocaína por frotación sobre la zona afectada. En este estudio se utilizaron 40 ratas de la cepa Wistar (20 experimentales y 20 control) durante 16 semanas. Se demostró que la cocaína produce alteraciones clínicas e histológicas en la encía, siendo la gingivitis crónica la patología más frecuente en un 70 por ciento de los casos, por lo cual se debe considerar en la evaluación clínica el consumo de drogas como factor de riesgo de la enfermedad periodontal (AU)