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Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro

机译:人多能干细胞在体外定向分化为肠道组织

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Studies in embryonic development have guided successful efforts to direct the differentiation of human embryonic and induced pluripotent stem cells (PSCs) into specific organ cell types in vitro. For example, human PSCs have been differentiated into monolayer cultures of liver hepatocytes and pancreatic endocrine cells that have therapeutic efficacy in animal models of liver disease and diabetes, respectively. However, the generation of complex three-dimensional organ tissues in vitro remains a major challenge for translational studies. Here we establish a robust and efficient process to direct the differentiation of human PSCs into intestinal tissue in vitro using a temporal series of growth factor manipulations to mimic embryonic intestinal development. This involved activin-induced definitive endoderm formation, FGF/ Wnt-induced posterior endoderm pattering, hindgut specification and morphogenesis, and a pro-intestinal culture system15'16 to promote intestinal growth, morphogenesis and cytodifferentia-tion. The resulting three-dimensional intestinal 'organoids' con-sisted of a polarized, columnar epithelium that was patterned into villus-like structures and crypt-like proliferative zones that expressed intestinal stem cell markers. The epithelium contained functional enterocytes, as well as goblet, Paneth and enteroendo-crine cells. Using this culture system as a model to study human intestinal development, we identified that the combined activity of WNT3A and FGF4 is required for hindgut specification whereas FGF4 alone is sufficient to promote hindgut morphogenesis. Our data indicate that human intestinal stem cells form de novo during development. We also determined that NEUROG3, a pro-endocrine transcription factor that is mutated in enteric anendocrinosis, is both necessary and sufficient for human enteroendocrine cell development in vitro. PSC-derived human intestinal tissue should allow for unprecedented studies of human intestinal development and disease.
机译:胚胎发育的研究指导了成功的努力,以指导人类胚胎和诱导多能干细胞(PSC)在体外分化为特定器官细胞类型。例如,人类PSC已分化为分别在肝病和糖尿病动物模型中具有治疗功效的肝肝细胞和胰腺内分泌细胞的单层培养物。然而,体外复杂的三维器官组织的产生仍然是转化研究的主要挑战。在这里,我们建立了一个强大而有效的过程,可使用人为的PSC分化为体外的肠道组织,并使用一系列的生长因子操作来模拟胚胎肠道的发育。这涉及激活素诱导的定形内胚层形成,FGF / Wnt诱导的后内胚层模式,后肠规格和形态发生,以及促进肠生长,形态发生和细胞分化的前肠培养系统15'16。产生的三维肠“类器官”由极化的柱状上皮组成,该上皮被图案化为表达肠干细胞标记的绒毛状结构和隐窝状增生区。上皮细胞含有功能性肠上皮细胞,以及杯状细胞,Paneth细胞和肠内分泌细胞。使用此培养系统作为模型来研究人类肠道发育,我们确定了WNT3A和FGF4的结合活性是后肠规格所必需的,而单独的FGF4足以促进后肠形态发生。我们的数据表明人类肠道干细胞在发育过程中从头形成。我们还确定,NEUROG3,一种在肠内分泌内毒素中发生突变的前内分泌转录因子,对于人类体外肠内分泌细胞的发育既是必需的又是足够的。 PSC衍生的人类肠道组织应允许对人类肠道发育和疾病进行前所未有的研究。

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  • 来源
    《Nature》 |2011年第7332期|p.105-109|共5页
  • 作者单位

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Hematology and Oncology Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA,Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Hematology and Oncology Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA,Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

    Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, Ohio 45229-3039, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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