钠-钾-氯离子协同转运子--2(NKCC2)对牙釉质发育的影响

基本信息
批准号:81400475
项目类别:青年科学基金项目
资助金额:23.00
负责人:郭婧
学科分类:
依托单位:浙江中医药大学
批准年份:2014
结题年份:2017
起止时间:2015-01-01 - 2017-12-31
项目状态: 已结题
项目参与者:霍光,郑园娜,柳毅,郑胜
关键词:
牙釉质氯离子协同转运子2釉质发育离子通道
结项摘要

Different ion channels, which play an important role in the tooth development, are found to be expressed in the tooth germ and tissues. Our previous researches showed that the ion channels on the mature ameloblasts responsible for the pH regulation and the transport of calcium and phosphate to build the enamel prism are inevitable for the enamel formation. Furthermore, our data suggested that ameloblasts used NKCX4 and NaPi to transport mineral ions into enamel in cotransport or exchange with K+ and Na+,which are needed to be recycled back from enamel into the ameloblasts. NKCC2, which work as K+, Na+ and Cl- cotransporter is positively stained in mature ameloblast by immunostaining method. Thus, we hypothesize that NKCC2 affect the enamel formation by helping realizing the functions of other important ion channels, such as pH regulator and Ca and P transporters. In this proposal, we will use the following methods to investigate the effects of NKCC2 on the enamel formation. Firstly, localize the expression of NKCC2 on the mature ameloblasts by immunohistochemistry. Secondly, we will test the effect of NKCC2 on the differentiation and function of mature ameloblast in vitro. Thirdly, we will investigate the enamel phenotype by inhibiting the function of NKCC2 in vivo. The results of this project will facilitate understanding the pathology of NKCC2- related dental channelopathy.

离子通道对牙齿发育起着重要调控。我们前期研究:由成熟型成釉细胞上的AE2、CFTR离子通道介导的对釉质空间pH调节以及由NKCX和NaPi离子通道所介导的钙磷离子转运机制对釉质发育至关重要。我们已证实:钠-钾-氯离子协同转运子-2在成熟型成釉细胞表达。而NKCC2 可能通过将NKCX和NaPi离子通道转运至釉质中的Cl-、Na+与K+重新转运至细胞内来影响上述离子通道。本课题探讨NKCC2在釉质发育中的作用:1)通过免疫组织化学及激光共聚焦技术研究NKCC2在釉质发育过程中时间和空间表达规律;2)成釉细胞体外培养模型中,利用呋塞米抑制NKCC2,通过RT-PCR等技术检测NKCC2对于与成熟型成釉细胞分化与功能状态相关基因、蛋白和离子转运影响;3)体内功能抑制的方式研究NKCC2对釉质发育作用表型。本项目明确NKCC2对釉质发育影响及相关离子疾病病理机制研究提供理论依据。

项目摘要

本项目在4周龄SD大鼠下颌切牙的组织切片,通过免疫组织化学的方法,明确了NKCC2在大鼠成釉细胞上确实存在表达。通过激光共聚焦技术,利用各细胞器表面特异抗体与NKCC2共染色的方法,明确出了NKCC2具体表达部位。将大鼠标本切片后,将组织切片进行抗NKCC2的免疫染色,通过与对照组比较,观察出NKCC2在大鼠成釉细胞上有大量所表达。利用激光共聚焦显微镜观察NKCC2阳性的位置并确定NKCC2表达的具体位置。.此外我们体外培养胚胎大鼠成釉器来源的HAT-7细胞系,模拟上皮来源的成釉细胞在体内所形成的单层结构,以建立与体内生理状态高度相似的模型来研究成釉细胞不同侧细胞膜上的转运通道的功能。.通过与荷兰阿姆斯特丹牙科中心口腔生物系开展合作获赠了大鼠成釉器来源的HAT-7细胞系,经过条件摸索,使用transwell培养板,诱导该细胞。成功诱导出形成单层且具有极化的成熟型成釉细胞。此为本课题组本项目研发并已可成熟运用的技术。.利用抗Zo1,Zo2和Claudin1等上皮细胞间紧密连接的标志抗体对细胞进行免疫荧光染色,利用激光共聚焦技术,发现该单层细胞对Zo1,Zo2和Claudin1等上皮细胞间紧密连接的标志均呈现阳性表达。本项目最终成功完成预期实验项目,并成功构建单层极化成熟型成釉细胞培养体系,验证NKCC2对成熟型成釉细胞的具有非常重要的生物学作用。依托本项目发表SCI 论文3篇。

项目成果
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数据更新时间:2023-05-31

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