Neurobiology of Intrinsic Primary Afferent Neurons

内在初级传入神经元的神经生物学

基本信息

  • 批准号:
    10275133
  • 负责人:
  • 金额:
    $ 58.75万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-09-01 至 2025-06-30
  • 项目状态:
    未结题

项目摘要

Project Summary / Abstract The gastrointestinal (GI) tract is the only organ system that is capable of intrinsic neural reflexes. These are initiated by a unique neuron type called intrinsic primary afferent neurons (IPANs). IPANs are key to orchestrating neural reflexes that allow efficient processing of meals for nutrient uptake by rapidly adapting to changing luminal content to alter vascular, secretory and motor function. In the guinea pig, IPANs use multiple mechanisms of neuroplasticity to adapt to inflammatory, hormonal and neural stimuli. From these studies it is clear that IPAN neuroplasticity mediates digestive disease. Even though the mouse has become the vertebrate animal model of choice for digestive disease, murine IPANs have lacked consensus markers making precise studies of mouse IPANs inconceivable. These issues are now resolved by our recent transcriptome and morphological analysis of the ENS, which challenges the dogma that IPANs are a single class of neuron, and suggest that rather there are four classes of IPANs. In combination with recent advances in morphological (i.e. tissue clearing) and physiological approaches (i.e. genetically-encoded markers and activity indicators) we are now able to study mouse IPANs in a relatively high throughput manner. The objective of this proposal is to test the overall hypothesis that different classes of IPANs possess morphologies and physiology that uniquely contribute to intestinal function. This hypothesis will be tested in a series of experiments designed to address three specific aims: Specific Aim 1: determine the structure of receptive fields and connectivity of murine IPANs; Specific Aim 2: determine responses of murine IPANs to mechanical and chemical stimuli; Specific Aim 3: determine the role of IPANs in gastrointestinal physiology. Collectively, these studies address a critical gap in our knowledge on the basic neural control of gut functions. Deciphering sensory capabilities and functional responses of molecularly defined IPANs are likely to pave the way for future improvements in diagnostic and therapeutic strategies of digestive disease.
项目总结/摘要 胃肠道(GI)是唯一能够进行内在神经反射的器官系统。这些是 由一种独特的神经元类型发起,称为内在初级传入神经元(IPAN)。IPAN是 协调神经反射,通过快速适应 改变管腔内容物以改变血管、分泌和运动功能。在豚鼠中,IPAN使用多个 神经可塑性机制,以适应炎症,激素和神经刺激。从这些研究来看, 明确IPAN神经可塑性介导消化系统疾病。即使老鼠已经变成了脊椎动物 作为消化系统疾病的动物模型选择,鼠IPAN缺乏一致的标志物, 对小鼠IPAN的研究是不可思议的。我们最近的转录组解决了这些问题, ENS的形态学分析,它挑战了IPAN是单一类别神经元的教条, 这表明IPAN有四种类型。结合形态学的最新进展(即 组织清除)和生理学方法(即遗传编码的标记物和活性指示物), 现在能够以相对高通量的方式研究小鼠IPAN。本提案的目的是测试 不同类别的IPAN具有独特的形态学和生理学, 有助于肠道功能。这一假设将在一系列旨在解决 三个具体目标:具体目标1:确定小鼠感受野的结构和连接 IPAN;特异性目标2:确定小鼠IPAN对机械和化学刺激的反应;特异性目标 3:确定IPAN在胃肠道生理学中的作用。总的来说,这些研究解决了一个关键的差距, 我们对肠道功能的基本神经控制的了解。解读感官能力和功能 分子定义的IPAN的反应可能为未来诊断和治疗的改进铺平道路。 消化系统疾病的治疗策略。

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 }}

David R. Linden其他文献

Su1212 THE ELECTROGENIC SODIUM/BICARBONATE COTRANSPORTER SLC4A4 IS REQUIRED FOR SLOW WAVE (SW) GENERATION BY INTERSTITIAL CELLS OF CAJAL (ICC) BUT IS NOT SOLELY RESPONSIBLE FOR THE EFFECTS OF BICARBONATE ON SW ACTIVITY
  • DOI:
    10.1016/s0016-5085(24)02067-5
  • 发表时间:
    2024-05-18
  • 期刊:
  • 影响因子:
  • 作者:
    Natalie R. Wertish;Peter R. Strege;Siva Arumugam Saravanaperumal;Cheryl Bernard;Gianluca Cipriani;David R. Linden;Linda C. Hsi;Michael F. Romero;Gianrico Farrugia;Tamas Ordog
  • 通讯作者:
    Tamas Ordog
Su1236 TRP53-MEDIATED CELL CYCLE ARREST OF PRECURSORS RATHER THAN CELLULAR SENESCENCE UNDERLIES INTERSTITIAL CELL OF CAJAL DEPLETION DURING AGING
  • DOI:
    10.1016/s0016-5085(20)32084-9
  • 发表时间:
    2020-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Yujiro Hayashi;David R. Linden;Siva Arumugam Saravanaperumal;Yoshitaka Toyomasu;Simon J. Gibbons;Huihuang Yan;Gianrico Farrugia;Tamas Ordog
  • 通讯作者:
    Tamas Ordog
111 Altered P<sub>2</sub>X<sub>3</sub> Receptors in Prevertebral Ganglia During Colitis Is Dependent on Mammalian Target of Rapamycin
  • DOI:
    10.1016/s0016-5085(13)60091-8
  • 发表时间:
    2013-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    David R. Linden
  • 通讯作者:
    David R. Linden
561 OPTOGENETIC STIMULATION OF INTESTINAL ENTEROENDOCRINE CELLS CAUSES EPITHELIAL CHLORIDE SECRETION THROUGH NEUROGENIC AND PARACRINE MECHANISMS
  • DOI:
    10.1016/s0016-5085(23)01202-7
  • 发表时间:
    2023-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Aura S. Ortegon Nino;Kaitlyn R. Knutson;Xi Yu;Halil S. Kacmaz;Anthony J. Treichel;Gianrico Farrugia;Arthur Beyder;David R. Linden
  • 通讯作者:
    David R. Linden
671 MECHANOSENSITIVE ENTEROENDOCRINE CELLS REGULATE FORCE-INDUCED EPITHELIAL SECRETION
  • DOI:
    10.1016/s0016-5085(21)01065-9
  • 发表时间:
    2021-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Isabelle W. Finholm;Anthony J. Treichel;Kaitlyn R. Knutson;Madhusudan Grover;David R. Linden;Andrew B. Leiter;Gianrico Farrugia;Arthur Beyder
  • 通讯作者:
    Arthur Beyder

David R. Linden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('David R. Linden', 18)}}的其他基金

Mayo Clinic Research Education Program in Computational Autonomic Neurobiology of Diabetes and Digestive and Kidney Diseases
梅奥诊所糖尿病、消化和肾脏疾病计算自主神经生物学研究教育项目
  • 批准号:
    10709578
  • 财政年份:
    2022
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
  • 批准号:
    10477437
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
  • 批准号:
    10680037
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
  • 批准号:
    10654779
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neuroregeneration in the Enteric Nervous System
肠神经系统的神经再生
  • 批准号:
    8937180
  • 财政年份:
    2015
  • 资助金额:
    $ 58.75万
  • 项目类别:
Little Brain Big Brain Meeting
小脑大脑会议
  • 批准号:
    7745365
  • 财政年份:
    2009
  • 资助金额:
    $ 58.75万
  • 项目类别:
Extrinsic Neural Control of Gastrointestinal Function in the Disordered Bowel
肠道紊乱胃肠功能的外在神经控制
  • 批准号:
    8033223
  • 财政年份:
    2008
  • 资助金额:
    $ 58.75万
  • 项目类别:
Extrinsic Neural Control of Gastrointestinal Function in the Disordered Bowel
肠道紊乱胃肠功能的外在神经控制
  • 批准号:
    8217087
  • 财政年份:
    2008
  • 资助金额:
    $ 58.75万
  • 项目类别:
Extrinsic Neural Control of Gastrointestinal Function in the Disordered Bowel
肠道紊乱胃肠功能的外在神经控制
  • 批准号:
    7595197
  • 财政年份:
    2008
  • 资助金额:
    $ 58.75万
  • 项目类别:
Myenteric Neuroplasticity Due to Experimental Colitis
实验性结肠炎引起的肌间神经可塑性
  • 批准号:
    6524630
  • 财政年份:
    2002
  • 资助金额:
    $ 58.75万
  • 项目类别:

相似海外基金

How Spinal Afferent Neurons Control Appetite and Thirst
脊髓传入神经元如何控制食欲和口渴
  • 批准号:
    DP220100070
  • 财政年份:
    2023
  • 资助金额:
    $ 58.75万
  • 项目类别:
    Discovery Projects
The mechanisms of the signal transduction from brown adipocytes to afferent neurons and its significance.
棕色脂肪细胞向传入神经元的信号转导机制及其意义。
  • 批准号:
    23K05594
  • 财政年份:
    2023
  • 资助金额:
    $ 58.75万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
GPR35 on Vagal Afferent Neurons as a Peripheral Drug Target for Treating Diet-Induced Obesity
迷走神经传入神经元上的 GPR35 作为治疗饮食引起的肥胖的外周药物靶点
  • 批准号:
    10315571
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
  • 批准号:
    10477437
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
  • 批准号:
    10680037
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Neurobiology of Intrinsic Primary Afferent Neurons
内在初级传入神经元的神经生物学
  • 批准号:
    10654779
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
GPR35 on Vagal Afferent Neurons as a Peripheral Drug Target for Treating Diet-Induced Obesity
迷走神经传入神经元上的 GPR35 作为治疗饮食引起的肥胖的外周药物靶点
  • 批准号:
    10470747
  • 财政年份:
    2021
  • 资助金额:
    $ 58.75万
  • 项目类别:
Roles of mechanosensory ion channels in myenteric intrinsic primary afferent neurons
机械感觉离子通道在肌间固有初级传入神经元中的作用
  • 批准号:
    RGPIN-2014-05517
  • 财政年份:
    2018
  • 资助金额:
    $ 58.75万
  • 项目类别:
    Discovery Grants Program - Individual
Roles of mechanosensory ion channels in myenteric intrinsic primary afferent neurons
机械感觉离子通道在肌间固有初级传入神经元中的作用
  • 批准号:
    RGPIN-2014-05517
  • 财政年份:
    2017
  • 资助金额:
    $ 58.75万
  • 项目类别:
    Discovery Grants Program - Individual
Astrocytic discharge modulation of primary trigeminal afferent neurons and its potential role in orofacial chronic pain.
原发性三叉神经传入神经元的星形胶质细胞放电调节及其在口面部慢性疼痛中的潜在作用。
  • 批准号:
    386557
  • 财政年份:
    2017
  • 资助金额:
    $ 58.75万
  • 项目类别:
    Studentship Programs
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了