Human Organoid Model To Generate Mucosal Immune Cell Populations

产生粘膜免疫细胞群的人体类器官模型

基本信息

  • 批准号:
    NC/X002497/1
  • 负责人:
  • 金额:
    $ 25.23万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2023
  • 资助国家:
    英国
  • 起止时间:
    2023 至 无数据
  • 项目状态:
    未结题

项目摘要

Innate lymphoid cells (ILC) are a type of white blood cell that mainly reside inside organs such as the lungs and the gut. There is a lot of interest in these cells as they have been shown to play important roles in maintaining health and in fighting infections and cancer. Additionally, under certain conditions they have also been shown to drive disease progression. Despite their many roles in the body, ILC exist in small numbers in distant and hard to access tissues, so it is difficult to obtain enough cells to study them. This means that most researchers turn to the use of animals, such as mice, for their studies as ILC are much easier to obtain this way. This project aims to establish a technology by which to generate human ILC in sufficient numbers for experimental studies and can therefore be used to replace the need for mouse models. Recently, we discovered that organoids, these are mini-organs grown in the lab in a dish, are able to support the generation of large numbers of human ILC. We can easily obtain cells that have the capacity to become ILC (ILC precursors) from blood. Then, we add these precursor cells to the mini-organs where they are able to grow and fully development into ILC. Moreover, the type of mini-organ used is important for the development of these cells. The ILC grown in mini-guts are similar to ILC taken straight from the human the gut whilst ILC that grow in mini-lungs are similar to those taken from the lung. With this project we aim to further develop and validate this technology by analysing in detail the characteristics of the ILC that grow in our mini-organs. This will provide reassurance to the scientific community that these cells are able to accurately resemble the ILC found in the human body and so other scientists can confidently use this technology to grow cells for their studies.By doing this we aim for this technology to be widely adopted by the scientific community leading to ILC generated in our mini-organs to replace the use of mouse ILC in certain studies. As this technology advances, so will the number of studies in which this model will be able to be used instead of mice. Moreover, our technology has the additional benefit that as the cells being used are taken from humans they are able to more accurately model the roles of ILC in human health and disease
先天性淋巴样细胞(ILC)是一种白色血细胞,主要存在于肺和肠道等器官内。人们对这些细胞很感兴趣,因为它们已被证明在维持健康和对抗感染和癌症方面发挥着重要作用。此外,在某些情况下,它们也被证明会推动疾病进展。尽管ILC在体内有许多作用,但它们在遥远且难以接近的组织中存在数量很少,因此很难获得足够的细胞来研究它们。这意味着大多数研究人员转向使用动物(如小鼠)进行研究,因为ILC更容易通过这种方式获得。该项目旨在建立一种技术,通过该技术可以产生足够数量的人类ILC用于实验研究,因此可以用于取代对小鼠模型的需求。最近,我们发现类器官,这些是在实验室培养皿中生长的微型器官,能够支持大量人类ILC的产生。我们可以很容易地从血液中获得有能力成为ILC(ILC前体)的细胞。然后,我们将这些前体细胞添加到微型器官中,在那里它们能够生长并完全发育成ILC。此外,使用的微型器官的类型对于这些细胞的发育很重要。在微型肠中生长的ILC类似于直接从人肠中获取的ILC,而在微型肺中生长的ILC类似于从肺中获取的ILC。通过这个项目,我们的目标是通过详细分析在我们的微型器官中生长的ILC的特征来进一步开发和验证这项技术。这将为科学界提供保证,这些细胞能够准确地模拟人体中发现的ILC,因此其他科学家可以放心地使用这项技术来培养细胞用于他们的研究。通过这样做,我们的目标是这项技术被科学界广泛采用,从而在我们的微型器官中产生ILC,以取代某些研究中使用的小鼠ILC。随着这项技术的进步,这种模型能够代替小鼠的研究数量也会增加。此外,我们的技术还有一个额外的好处,因为所使用的细胞来自人类,它们能够更准确地模拟ILC在人类健康和疾病中的作用。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

Joana F Neves其他文献

CD27 is a thymic determinant of the balance between interferon-γ- and interleukin 17–producing γδ T cell subsets
CD27 是调节产生干扰素-γ和白细胞介素 17 的γδT 细胞亚群之间平衡的胸腺决定因素
  • DOI:
    10.1038/ni.1717
  • 发表时间:
    2009-03-08
  • 期刊:
  • 影响因子:
    27.600
  • 作者:
    Julie C Ribot;Ana deBarros;Dick John Pang;Joana F Neves;Victor Peperzak;Scott J Roberts;Michael Girardi;Jannie Borst;Adrian C Hayday;Daniel J Pennington;Bruno Silva-Santos
  • 通讯作者:
    Bruno Silva-Santos

Joana F Neves的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('Joana F Neves', 18)}}的其他基金

The crosstalks between immune cells, bacteria and epithelial cells in the intestine: elucidating their cellular and molecular mechanisms
肠道内免疫细胞、细菌和上皮细胞之间的串扰:阐明它们的细胞和分子机制
  • 批准号:
    MR/R024812/1
  • 财政年份:
    2017
  • 资助金额:
    $ 25.23万
  • 项目类别:
    Fellowship

相似国自然基金

幽门螺杆菌lnc1—miR-520通过p65激活PUMA启动caspase凋亡通路促进胃 organoid损伤的机制研究
  • 批准号:
    81770561
  • 批准年份:
    2017
  • 资助金额:
    51.0 万元
  • 项目类别:
    面上项目
应用organoid疾病模型研究ASPM对神经发生的调控作用
  • 批准号:
    31600840
  • 批准年份:
    2016
  • 资助金额:
    20.0 万元
  • 项目类别:
    青年科学基金项目

相似海外基金

Tractable human distal lung organoid model as a new efficient tool to study mesenchymal-epithelial interactions in COPD
易处理的人远端肺类器官模型作为研究慢性阻塞性肺病间充质-上皮相互作用的新有效工具
  • 批准号:
    NC/Y500641/1
  • 财政年份:
    2024
  • 资助金额:
    $ 25.23万
  • 项目类别:
    Training Grant
Elucidating Pathogenesis Heterogeneity of Type III Secretion System at The Single-Cell Level of Human iPSC-Derived Organoid Model
在人类 iPSC 衍生类器官模型的单细胞水平上阐明 I​​II 型分泌系统的发病机制异质性
  • 批准号:
    23K14170
  • 财政年份:
    2023
  • 资助金额:
    $ 25.23万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Human organoid model for COVID-19 myocarditis
COVID-19 心肌炎的人体类器官模型
  • 批准号:
    10746509
  • 财政年份:
    2023
  • 资助金额:
    $ 25.23万
  • 项目类别:
Interrogation of links between risks and early pathogenesis at single cell resolution in a novel human ALS organoid neuraxis model
在新型人类 ALS 类器官神经轴模型中以单细胞分辨率探讨风险与早期发病机制之间的联系
  • 批准号:
    MR/X006867/1
  • 财政年份:
    2023
  • 资助金额:
    $ 25.23万
  • 项目类别:
    Fellowship
Pluripotent stem cell-derived organoid model of human gonad development, functions, and disorders
人类性腺发育、功能和疾病的多能干细胞衍生类器官模型
  • 批准号:
    10816755
  • 财政年份:
    2023
  • 资助金额:
    $ 25.23万
  • 项目类别:
Advanced Human Pluripotent Stem Cell Kidney Organoid Model for Investigating Development and Disease
用于研究发育和疾病的先进人类多能干细胞肾类器官模型
  • 批准号:
    NC/X002047/1
  • 财政年份:
    2023
  • 资助金额:
    $ 25.23万
  • 项目类别:
    Research Grant
Developing a Human-Based Chimeric Retinal Organoid Model for use in Stem Cell Treatment Discovery for Inherited Retinal Diseases
开发基于人的嵌合视网膜类器官模型,用于发现遗传性视网膜疾病的干细胞治疗
  • 批准号:
    486596
  • 财政年份:
    2022
  • 资助金额:
    $ 25.23万
  • 项目类别:
    Studentship Programs
Determining the optimal ion and fractionation scheme for the treatment of GBM in a comprehensive human organoid model
在综合人体类器官模型中确定治疗 GBM 的最佳离子和分级方案
  • 批准号:
    10360627
  • 财政年份:
    2021
  • 资助金额:
    $ 25.23万
  • 项目类别:
Human Brain Organoid: a new CNSTB model
人脑类器官:一种新的 CNSTB 模型
  • 批准号:
    10453987
  • 财政年份:
    2021
  • 资助金额:
    $ 25.23万
  • 项目类别:
Leveraging 3D bioprinted organoid constructs to pattern and model human brain development
利用 3D 生物打印类器官结构来模拟人类大脑发育
  • 批准号:
    10184225
  • 财政年份:
    2021
  • 资助金额:
    $ 25.23万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了