Eda/Edar Regulation of Embryonic SMG Development

胚胎 SMG 发育的 Eda/Edar 调节

• 批准号: 7248802
• 负责人: TINA JASKOLL
• 金额: $ 37.48万
• 依托单位: UNIVERSITY OF SOUTHERN CALIFORNIA
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-01 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7248802
• 关键词: Acinar Cell; Aging; Amendment; Anhidrotic Ectodermal Dysplasia; Apoptosis; Cell Proliferation; Data; Development; Disease; Drug Design; Ectodermal Dysplasia; Embryo; Epithelium; Future; Genes; Hair; In Vitro; Link; Mediating; Methodology; Microanatomy; Molecular; Morphogenesis; Mucins; Mus; Mutant Strains Mice; Mutation; Outcome; Pathway interactions; Patients; Phenotype; Proteins; Proteomics; Receptor Gene; Regulation; Role; Salivary Glands; Signal Transduction; Staging; Sweat Glands; Tooth structure; Transgenic Mice; Transgenic Organisms; base; design; functional genomics; in vivo; indexing; loss of function; mutant; protein expression; spatiotemporal; transcriptomics

DESCRIPTION (provided by applicant): Hypohidrotic (anhidrotic) ectodermal dysplasia (HED), the most common of the approximately 150 described ectodermal dysplasias, is a disorder characterized by abnormal development of hair, teeth, sweat glands and salivary glands. Mutations in the: EDA and EDAR (EDA receptor) genes are responsible for X-linked and autosomal HED, respectively; abnormal phenotypes similar to HED are seen in Tabby (Eda-Ta) and downless (Edar-dl) mutant mice. Given the observation of abnormal submandibular salivary glands (SMG) in patients with HED and, similarly, in Tabby (Ta) and downless mice, our immunolocalization:of Eda and Edar proteins on embryonic SMG epithelia, and that our finding enhanced or interrupted Eda/Edar signaling in vitro modulates SMG branching morphogenesis, we postulate that Ecla/Edar signal transduction is essential for SMG development. To delineate the role of Eda/Edar signaling during embryonic SMG development, WE PROPOSE to: (a) Determine the progressive, stage-dependent phenotypic outcome of abrogated Eda/Edar signaling in embryonic Ta mutant SMGs and compare it to that seen in wildtype (WT) and gene-restored Tabby-EDA-A1 transgenic mouse SMGs. SMG phenotypes will be defined by microanatomy, cell proliferation and apoptosis indices, level of NFkappaB activation, and mucin protein expression. (b) Delineate the functional genomics of abrogated Eda/Edar/NFkappaB signaling in embryonic Ta SMGs, as compared to WT and Tabby-EDA-A1 transgenic mouse SMGs, using transcriptomic and proteomic methodologies. (c) Identify the functional pathways directly or collaterally downstream of the Eda/Edar/NFkappaB signal by comparing changes in activated protein expression in embryonic Ta, WT, and Tabby-EDA-A1 SMGs. Finally, we will delineate the in vivo spatiotemporal distribution of activated proteins: modulated with interrupted Eda/Edar/NFkappaB signaling. The data generated by our proposed studies will provide the framework for future studies of SMG loss of function and will provide a rational basis for designing drugs that may be used to restore acinar form and function in damaged and aging SMGs.

描述（由申请人提供）：少汗（无汗）外胚层发育不良（HED）是约150种描述的外胚层发育不良中最常见的一种，是一种以毛发、牙齿、汗腺和唾液腺发育异常为特征的疾病。突变：EDA和EDAR（EDA受体）基因分别导致X连锁和常染色体HED;在Tabby（Eda-Ta）和downless（Edar-dl）突变小鼠中观察到与HED相似的异常表型。考虑到HED患者以及Tabby（Ta）和无绒毛小鼠中异常下颌下唾液腺（SMG）的观察结果，我们的免疫定位：胚胎SMG上皮细胞上的Eda和Edar蛋白，以及我们的发现增强或中断的Eda/Edar信号在体外调节SMG分支形态发生，我们推测Ecla/Edar信号转导对SMG发育至关重要。为了描述Eda/Edar信号在胚胎SMG发育过程中的作用，我们建议：（a）确定胚胎Ta突变SMG中废除Eda/Edar信号的进行性、阶段依赖性表型结果，并将其与野生型（WT）和基因恢复的Tabby-EDA-A1转基因小鼠SMG中观察到的结果进行比较。SMG表型将通过显微解剖学、细胞增殖和凋亡指数、NF κ B活化水平和粘蛋白表达来定义。(b)使用转录组学和蛋白质组学方法，与WT和Tabby-EDA-A1转基因小鼠SMG相比，描绘胚胎Ta SMG中废除的Eda/Edar/NF κ B信号传导的功能基因组学。(c)通过比较胚胎Ta、WT和Tabby-EDA-A1 SMG中活化蛋白表达的变化，鉴定Eda/Edar/NF κ B信号直接或间接下游的功能通路。最后，我们将描绘在体内的时空分布的激活蛋白质：调制中断的EDA/Edar/NF κ B信号。我们提出的研究产生的数据将为SMG功能丧失的未来研究提供框架，并将为设计可用于恢复受损和老化SMG中腺泡形式和功能的药物提供合理的基础。

项目成果

Salivary gland branching morphogenesis: a quantitative systems analysis of the Eda/Edar/NFkappaB paradigm.

• DOI: 10.1186/1471-213x-9-32
• 发表时间: 2009-06-06
• 期刊: BMC developmental biology
• 作者: Melnick M;Phair RD;Lapidot SA;Jaskoll T
• 通讯作者: Jaskoll T

Cytomegalovirus induces abnormal chondrogenesis and osteogenesis during embryonic mandibular development.

巨细胞病毒在胚胎下颌发育过程中诱导异常软骨生成和骨生成。

• DOI: 10.1186/1471-213x-8-33
• 发表时间: 2008-03-27
• 期刊: BMC DEVELOPMENTAL BIOLOGY
• 作者: Jaskoll, Tina;Abichaker, George;Sedghizadeh, Parish P.;Bringas, Pablo, Jr.;Melnick, Michael
• 通讯作者: Melnick, Michael