Regulation of mammary branching morphogenesis by Slit/Robo1 signaling

Slit/Robo1 信号传导对乳腺分支形态发生的调节

• 批准号: 8325062
• 负责人: LINDSAY E HINCK
• 金额: $ 37.32万
• 依托单位: UNIVERSITY OF CALIFORNIA SANTA CRUZ
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-29 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8325062
• 关键词: 3-Dimensional; Adhesives; Basal Cell; Biochemical; Biological; Biological Models; Biology; Breast; Cancer Biology; Cancer Etiology; Cell Adhesion; Cell Nucleus; Cell Proliferation; Cell physiology; Cells; Cessation of life; Complex; Cues; DNA Sequence Rearrangement; Data; Development; Developmental Cell Biology; Environment; Epithelial; Extracellular Matrix Proteins; Family; Gland; Goals; Growth; Image; Knock-out; Knowledge; Malignant - descriptor; Malignant Neoplasms; Mammary gland; Mediating; Membrane; Modeling; Morphogenesis; Mus; Mutation; Myoepithelial cell; Neoplasm Metastasis; Noninfiltrating Intraductal Carcinoma; Organ; Organogenesis; Organoids; Outcomes Research; Pathway interactions; Phenotype; Play; Population; Primary Cell Cultures; Principal Investigator; Process; Prostate; Regulation; Reporting; Research; Role; Salivary; Signal Pathway; Signal Transduction; Signaling Molecule; Signaling Protein; Stem cells; Stratum Basale; Structure; System; Techniques; Testing; Tissues; Transcriptional Activation; Transforming Growth Factors; Transgenic Mice; Transplantation; Up-Regulation; WNT Signaling Pathway; Woman; cancer stem cell; cell growth; extracellular; gain of function; in vivo; infiltrating duct carcinoma; inhibitor/antagonist; loss of function mutation; malignant breast neoplasm; mammary epithelium; mammary gland development; mouse model; novel; progenitor; programs; protein function; receptor; research study; self-renewal; stem; tumor; tumor growth; tumor initiation; tumor progression; tumorigenesis

DESCRIPTION (provided by applicant): A core objective of tissue biology is to understand how cells interact to generate tissues and organs. While great strides have been made in defining signaling pathways that mediate cellular interactions, there is a fundamental gap in our knowledge concerning how these signaling systems are integrated during mammalian organogenesis. Bridging this knowledge gap is important in identifying druggable targets for cancer, as tumor growth and progression is marked by disorganization of tissue structure, and deregulation of specialized cell populations, such as stem cells. The goal of this application is to understand how extracellular factors, SLITs, influence tissue morphogenesis by regulating the proliferation of a single layer of basal cells in which stem cells reside. Here, mammary branching morphogenesis is used as a model system and, guided by strong preliminary data, the following model is investigated in which a key inhibitor of mammary branching, TGF-21, restrains basal cell proliferation and adhesion by upregulating signaling through the SLIT/ROBO1 pathway. This, in turn, controls basal cell growth and branching morphogenesis by increasing the adhesive functions of 2-catenin at the membrane, at the expense of its proliferative functions in the nucleus. A variety of cell biological, imaging and biochemical techniques will be employed, as well as powerful transplant techniques to manipulate genetically modified mammary tissue. Three hypotheses are tested in three Aims: I) that TGF-21 upregulates Robo1 expression, specifically in basal cells, and that this inhibits branching by restraining basal cell growth; II) that SLIT/ROBO1 signaling opposes the actions of canonical WNTs by altering the subcellular localization of 2-catenin and promoting its cell adhesive functions at the expense of its transcriptional functions; and III), that SLITs are non-renewal factors for stem cells that function to counter the self-renewal signals of canonical WNT signaling by regulating 2-catenin. Together, these experiments will have a positive impact on cancer biology of breast and other glandular organs containing basal stem cell subpopulations (e.g. prostate, salivary etc), because they delineate a novel tumor suppressive signaling network that appears to function in stem cells.

描述（由申请人提供）：组织生物学的核心目标是了解细胞如何相互作用以产生组织和器官。虽然在定义介导细胞相互作用的信号通路方面已经取得了很大的进展，但在哺乳动物器官发生过程中，这些信号系统是如何整合的，我们的知识还存在根本性的差距。弥合这一知识差距对于确定癌症的可药物靶点非常重要，因为肿瘤的生长和进展是以组织结构的紊乱和特化细胞群（如干细胞）的失调为特征的。本应用程序的目的是了解细胞外因子（SLITs）如何通过调节干细胞所在的单层基底细胞的增殖来影响组织形态发生。本研究以乳腺分支形态发生为模型系统，在强有力的初步数据指导下，研究了以下模型，其中乳腺分支的关键抑制剂TGF-21通过上调SLIT/ROBO1通路的信号来抑制基底细胞的增殖和粘附。这反过来又通过增加2-连环蛋白在膜上的粘附功能来控制基底细胞的生长和分支形态发生，而牺牲了其在细胞核中的增殖功能。将采用多种细胞生物学、成像和生化技术，以及强大的移植技术来操纵转基因乳腺组织。在三个目的下测试了三个假设：1)TGF-21上调Robo1的表达，特别是在基底细胞中，并且通过抑制基底细胞生长来抑制分支；II) SLIT/ROBO1信号通过改变2-catenin的亚细胞定位并以牺牲其转录功能为代价促进其细胞粘附功能，从而反对典型wnt的作用；III)，裂隙是干细胞的非更新因子，其功能是通过调节2-catenin来对抗典型WNT信号的自我更新信号。总之，这些实验将对乳腺癌和其他含有基底干细胞亚群（如前列腺、唾液等）的腺体器官的癌症生物学产生积极影响，因为它们描绘了一个新的肿瘤抑制信号网络，似乎在干细胞中起作用。