课题基金 / 基金详情

Engineering intestinal mucosal tissue grafts as a novel treatment for inflammatory bowel disease.

Engineering intestinal mucosal tissue grafts as a novel treatment for inflammatory bowel disease.
工程化肠粘膜组织移植作为炎症性肠病的新型治疗方法。
批准号:
MR/R017336/1
负责人:
William Dalleywater
金额:
$36.38万
依托单位:
依托单位国家:
英国
项目类别:
Fellowship
财政年份:
2018
资助国家:
英国
项目状态:
已结题
起止时间:
2018 至 --

项目摘要

项目成果

相似基金

相关文献

中文摘要
翻译
炎症性肠病是一种影响许多成年人的终身疾病,它可以在5岁的儿童中开始。这种疾病包括在肠道内形成溃疡和疤痕,导致疼痛、出血和腹泻。常见的治疗方法包括使用强效药物,但这些药物并不总是有效,而且有明显的副作用。如果病人对药物没有反应,那么手术通常是唯一的选择。手术包括切除肠道的病变部分,在严重的情况下可能需要结肠造口术,将肠道转移到身体外部,并将内容物排出到外部的造口袋中。虽然手术可以在短期内帮助减轻疾病症状,但它可能导致患者出现营养不良和维持水分的问题。此外,手术并不能治愈,一半的患者在第一次手术后的10年内需要进一步手术。炎症性肠病患者的生活质量可能非常差,因为目前的治疗方法往往不是完全有效,可能只提供暂时的缓解。因此,开发治疗炎症性肠病的新方法是紧迫和重要的。该项目的目的是利用干细胞技术和先进的材料和3D打印技术在实验室中开发替代肠道组织,这些组织可以作为移植物安全地插入大肠(结肠),从而避免造口,并可能恢复肠道功能。最近的研究已经使得将皮肤细胞转化为干细胞成为可能,干细胞可以形成身体的任何组织。由此可见,替代组织可以由患者自身的细胞产生,从而避免器官排斥的风险。要做到这一点,我需要建立使干细胞形成结肠细胞的条件。在概念验证研究中,我已经成功地在实验室培养了干细胞,形成了早期的结肠细胞。结合先进的3D打印技术,我将非常精确地设计具有表面的材料,这将进一步提高我们可以生产的肠细胞的质量。因此,我将致力于建立诱导多能干细胞向结肠细胞生长的最佳条件。在实验室里建立了如何在小范围内制造功能性肠道组织之后,我将制造更大的材料片,适合插入肠道。最后,我打算通过将实验室培养的组织移植物植入动物宿主的结肠来测试它们。这将使我能够确保他们按预期运作,安全并保持健康。这将提供一个原则性的证明,即这些细胞可以作为一种潜在的治疗方法植入人体肠道。干细胞研究与尖端材料工程的结合是一种新颖的方法。如果成功,它可能会导致炎症性肠病和其他需要手术治疗的肠道疾病的新治疗方法的发展。这个项目还将帮助我们了解肠道发育的机制。特别是,我将研究细胞生长的材料的特性如何影响它们的行为(这与患者特异性组织移植物的发展高度相关)。该组织还可以作为肠道疾病的实验室模型,用于研究疾病发展和测试其他治疗方法。
英文摘要
Inflammatory bowel disease is a life-long condition which affects many adults and which can begin in children as young as 5. This disease involves the formation of ulcers and scarring in the bowel which causes pain, bleeding and diarrhoea. Common treatment involves powerful drugs that do not always prove effective and have significant side effects. If patients do not respond to drugs then surgery is often the only option. Surgery involves removing diseased parts of bowel and in severe cases may require a colostomy where the intestines are diverted to the outside of the body and contents draining externally into a stoma bag. Whilst operations can help reduce disease symptoms in the short term, it may result in patients having problems with malnutrition and maintaining hydration. Additionally, surgery is not a cure and half of all patients require further surgery within 10 years of the first procedure.The quality of life for people with inflammatory bowel disease can be very poor as current treatments are often not completely effective and may only offer temporary respite. Developing new treatments for inflammatory bowel disease is thus urgent and important.The aim of this project is to utilise stem cells technology with advanced materials and 3D printing to develop replacement bowel tissue in the laboratory which can be safely inserted into the large bowel (colon) as a graft thereby avoiding a stoma and possibly restoring bowel function. Recent research has made it possible to take skin cells and turn them into stem cells which can form any tissue in the body. It follows from this that replacement tissue can be created from a patient's own cells which avoids the risk of organ rejection. To do this, I need to establish the conditions which make stem cells form the cells which line the colon. Already in proof of concept studies I have successfully grown stem cells in the laboratory to form early colon cells. Incorporating this with cutting-edge 3D printing technology, I will design materials very precisely with surfaces which will further enhance the quality of intestinal cells we can produce. I will therefore aim to establish the optimal conditions to make induced pluripotent stem cells to grow into colon cells. Having established how to create functional bowel tissue in the laboratory on a small scale, I will manufacture larger sheets of material which would be suitable for inserting into the bowel. Finally, I intend to test the laboratory grown tissue grafts by implanting them into the colon of an animal host. This will allow me to ensure they function as expected, are safe and remain healthy. This would provide proof-of-principle that these could be inserted into the bowel of humans as a potential treatment.The combination of stem cell research with cutting-edge materials engineering is a novel approach. If successful, it could lead to the development of a novel treatment in inflammatory bowel disease and in other bowel diseases where surgery is necessary. This project will also help us to understand the mechanisms driving bowel development. In particular, I will investigate how the characteristics of material on which cells grow influence their behaviour (which is highly relevant to the development of patient-specific tissue grafts). The tissue would also be valuable as a laboratory model of bowel disease to research disease development and to test other treatments.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
A New Forced Aggregation Method for Generating Embryoid Bodies from Mouse Embryonic Stem Cells
一种从小鼠胚胎干细胞中产生胚体的新强制聚集方法
DOI: --
发表时间: 2018
期刊:
影响因子: --
作者: [Dalleywater, WJ]
通讯作者: Dalleywater, WJ
Intestinal Stromal Cells Derived from Induced Pluripotent Stem Cells Show Heterogeneity and Remodelling Capabilities
诱导多能干细胞衍生的肠基质细胞表现出异质性和重塑能力
DOI: --
发表时间: 2021
期刊: JOURNAL OF PATHOLOGY
影响因子: 7.3
作者: [Dalleywater W.]
通讯作者: Dalleywater W.
A Novel 3D Cell Culture System Demonstrates Induced Pluripotent Stem Cells Driven to Intestinal Differentiation are Capable of Spontaneous Crypt Assembly.
新型 3D 细胞培养系统证明诱导多能干细胞驱动肠分化,能够自发地进行隐窝组装。
DOI: --
发表时间: 2019
期刊:
影响因子: --
作者: [Dalleywater, WJ]
通讯作者: Dalleywater, WJ
Collagen Hydrogel Matrices Permit Formation Of Mature Intestinal Mucosal Features In Cultures Of Ipsc-derived Intestinal Mucosal Cells.
胶原水凝胶基质允许在 Ipsc 衍生的肠粘膜细胞培养物中形成成熟的肠粘膜特征。
DOI: --
发表时间: 2019
期刊:
影响因子: --
作者: [Dalleywater, WJ]
通讯作者: Dalleywater, WJ
共 8 条
    国内基金
    海外基金
    西方饮食通过“肠道菌群-Rspo1”轴促进肥胖与肠道吸收的机制研究
    • 批准号:
      82370845
    • 项目类别:
      面上项目
    • 资助金额:
      48.00万元
    • 批准年份:
      2023
    • 负责人:
      洪洁
    • 依托单位:
    新生儿坏死性小肠结肠炎中去泛素化酶USP15调控ILC3分化损伤肠道粘膜屏障的致病机制研究
    • 批准号:
      82371711
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      吕志宝
    • 依托单位:
    “肠—肝轴”PPARα/CYP8B1胆汁酸合成信号通路在减重手术改善糖脂代谢中的作用与机制
    • 批准号:
      82370902
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      田景琰
    • 依托单位:
    短链脂肪酸上调小肠上皮紧密连接屏障功能的机制
    • 批准号:
      31040041
    • 项目类别:
      专项基金项目
    • 资助金额:
      10.0万元
    • 批准年份:
      2010
    • 负责人:
      王鹏远
    • 依托单位: