Mechanism of CTIP2 action in mouse epidermal homeostasis and barrier formation,

CTIP2在小鼠表皮稳态和屏障形成中的作用机制，

• 批准号: 8074982
• 负责人: Arup K. Indra
• 金额: $ 29.45万
• 依托单位: OREGON STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-26 至 2013-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8074982
• 关键词: Adult; Atopic Dermatitis; Biological; Biology; Biopsy; Body Weight; Cells; Communities; Data; Defect; Dehydration; Dermatology; Development; Disease; Electrolytes; Employee Strikes; Environment; Enzymes; Epithelial Cells; Equipment; Event; FOS gene; Failure; Fetal Development; Gene Expression; Goals; Head and Neck Squamous Cell Carcinoma; Health; Homeostasis; Human; Inflammatory; Inherited; Keratin; Knowledge; Laboratories; Lead; Learning; Life; Maintenance; Malignant Neoplasms; Molecular; Molecular Genetics; Mus; Neonatal; Organ; Outcome; Pathogenesis; Pathway interactions; Permeability; Phenotype; Play; Positioning Attribute; Premature Infant; Process; Proliferating; Proteins; Psoriasis; Research; Resources; Role; Skin; Skin Cancer; Testing; Thick; Time; Tissues; Transcription Regulatory Protein; Transcriptional Regulation; Up-Regulation; Water; Work; base; c-myc Genes; caspase 14; chicken ovalbumin upstream promoter-transcription factor; effective therapy; fetal; filaggrin; genetic regulatory protein; innovation; interest; keratinocyte; lipid biosynthesis; lipid metabolism; loricrin; mortality; mouse development; mouse model; skin disorder; skin organogenesis; transcription factor; transglutaminase 1; tumor; tumor initiation

DESCRIPTION (provided by applicant): The development of the skin from intrauterine to extrauterine life is an orchestrated interplay of epidermal proliferation, terminal differentiation, and barrier formation. Failure to construct an epidermal permeability barrier (EPB), which is a life-threatening problem in the majority of premature infants, results in increased transepidermal water loss with concomitant dehydration and electrolyte imbalance, as well as fragile skin. Barrier defects are also believed to contribute to several hereditary and acquired inflammatory skin disorders, such as psoriasis and atopic dermatitis (AD). Thus, understanding the pathways that are controlled by different regulatory proteins (e.g., transcription factors) in skin is the key for the development of effective treatments for the various skin diseases described above, as well as epithelial cell skin cancers, including head and neck squamous cell carcinoma (HNSCC). Chicken ovalbumin upstream promoter transcription factor (COUP-TF)-interacting protein 2 (CTIP2, also known as Bcl11b) is a transcriptional regulatory protein that is highly expressed in skin during mouse development, as well as in proliferating cells of the adult mouse. We have recently discovered that germline deletion of CTIP2 in mice results in a severe skin phenotype characterized by compromised EPB formation, and dramatically reduced epidermal thickness. We have also observed striking upregulation of CTIP2 in several human HNSCC biopsies, in which the level of CTIP2 expression was inversely correlated with the degree of differentiation of the tumor, i.e., poorly differentiated tumors were found to express very high levels of CTIP2 while highly differentiated tumors expressed very little CTIP2. However, the cellular and molecular mechanism underlying the activity of CTIP2 in skin during epidermal homeostasis and barrier formation is not known. Similarly, we do not understand the role of CTIP2 in proliferative events during skin development or in proliferative diseases of adults, such as HNSCC. Lack of this knowledge is a critical problem in our understanding of the biological roles of the CTIP2 in human health and disease. The long-term goal of this laboratory is to elucidate the molecular and cellular mechanisms that underlie the actions of CTIP2 in fetal, neonatal, and adult skin, and in proliferative diseases of the skin, towards the goal of extrapolating to the human situation. Based on the above observations and from the preliminary data, we propose the following three Specific Aims: (1) to elucidate the cellular and molecular mechanism(s) underlying the role of CTIP2 in EPB formation, (2) to elucidate the cellular and molecular mechanism(s) of CTIP2 action in epidermal proliferation/differentiation, and (3) to determine the role of CTIP2 in pathogenesis of head and neck squamous cell carcinoma. The proposed research is innovative because it will, for the first time, reveal the cellular and molecular mechanisms by which CTIP2 regulates skin organogenesis, EPB formation, and tissue homeostasis. We believe that this research will have significant, positive effects on human health because these outcomes will provide an enhanced understanding of regulatory influences on epidermal keratinocyte proliferation, differentiation and EPB formation, which may lead to development of more efficacious treatment paradigms for the human disorders, such as atopic dermatitis, and possibly HNSCC.

描述(由申请人提供)：皮肤从宫内到宫外的发育是表皮增殖、终末分化和屏障形成的精心安排的相互作用。未能构建表皮渗透屏障(EPB)是大多数早产儿的一个威胁生命的问题，会导致皮肤水分损失增加，并伴随着脱水和电解质失衡，以及脆弱的皮肤。屏障缺陷也被认为是几种遗传性和获得性炎症性皮肤病的原因，如牛皮癣和特应性皮炎(AD)。因此，了解皮肤中受不同调节蛋白(如转录因子)控制的途径是开发上述各种皮肤病以及包括头颈部鳞状细胞癌(HNSCC)在内的上皮细胞皮肤癌有效治疗方法的关键。鸡卵清蛋白上游启动子转录因子(COUP-TF)-相互作用蛋白2(CTIP2，又称Bcl11b)是一种转录调控蛋白，在小鼠发育过程中高表达于皮肤，在成年小鼠的增殖细胞中也高表达。我们最近发现，CTIP2在小鼠中的胚系缺失会导致严重的皮肤表型，其特征是EPB的形成受到影响，并显著降低表皮厚度。我们还观察到几例人HNSCC组织中CTIP2的表达显著上调，其中CTIP2的表达水平与肿瘤的分化程度呈负相关，即低分化肿瘤表达非常高的CTIP2，而高分化的肿瘤表达很低的CTIP2。然而，在表皮动态平衡和屏障形成过程中，CTIP2在皮肤中活性的细胞和分子机制尚不清楚。同样，我们不了解CTIP2在皮肤发育过程中的增殖事件中的作用，或者在成人增殖性疾病中的作用，如HNSCC。缺乏这方面的知识是我们理解CTIP2在人类健康和疾病中的生物学作用的一个关键问题。该实验室的长期目标是阐明CTIP2在胎儿、新生儿和成人皮肤以及皮肤增生性疾病中的作用背后的分子和细胞机制，以达到推断人类情况的目标。基于以上观察和初步数据，我们提出以下三个具体目标：(1)阐明CTIP2在EPB形成中的细胞和分子机制(S)；(2)阐明CTIP2在表皮增殖/分化中的细胞和分子机制(S)；(3)确定CTIP2在头颈部鳞状细胞癌发病机制中的作用。这项拟议的研究具有创新性，因为它将首次揭示CTIP2调节皮肤器官发生、EPB形成和组织动态平衡的细胞和分子机制。我们相信，这项研究将对人类健康产生重大的积极影响，因为这些结果将提供对表皮角质形成细胞增殖、分化和EPB形成调节影响的更好理解，这可能导致开发出更有效的人类疾病治疗方案，如特应性皮炎和可能的HNSCC。