Fluorinated Cell Surfaces to Modulate Biological Function

氟化细胞表面调节生物功能

• 批准号: 7618471
• 负责人: KRISHNA KUMAR
• 金额: $ 45.63万
• 依托单位: TUFTS UNIVERSITY MEDFORD
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-05-01 至 2012-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7618471
• 关键词: Adhesions; Biological; Biological Assay; Biological Process; Carbohydrates; Cell Adhesion; Cell physiology; Cell surface; Cells; Characteristics; Cleaved cell; Cultured Cells; Disease; Fluorine; Glycocalyx; Glycolipids; Glycoproteins; Goals; Image; Imaging Techniques; In Vitro; Incubated; Inflammation; Inflammatory; Interest Group; Life; Magnetic Resonance Imaging; Mediating; Modeling; Modification; Mus; Nature; Neoplasm Metastasis; Process; Property; Reaction; Sialic Acids; Spectrometry, Mass, Secondary Ion; Surface; Techniques; analog; cancer diagnosis; cancer therapy; chemical genetics; design; human disease; neoplastic cell; public health relevance; tumor

DESCRIPTION (provided by applicant): The goal of the proposed study is to explore the biological and biophysical properties of living cells that are decorated with unnatural fluorinated carbohydrates on their surfaces. It has been found that this cell-surface modification reduces cell adhesion, and therefore may provide a means to treat human disease processes that are mediated by cell adhesion such as tumor metastasis and inflammation. Part of this project is designed to determine the effect of cell-surface fluorine modification on biological functions related to cellular adhesion. The ability of fluorinated sialic acids to reduce the rate or extent of tumor metastasis will be studied by bioluminescent imaging in a murine model. The attachment of fluorinated molecules to the cell surface is accomplished by incubating the cells with chemically synthesized fluorinated sialic acid analogues that are taken up and processed into fluorinated glycoproteins and glycolipids expressed on the cell glycocalyx. Part of this project is to determine what the structural requirements are for a fluorinated sialic acid analogue to be expressed on the cell surface. Also, the distribution and nature of modified molecules on the cell surface will be determined by secondary ion mass spectrometry, by colorimetric assay of selectively cleaved cell-surface molecules, and by a chemical genetics approach. Since fluorinated molecules are virtually absent in unmodified cells, the incorporation of fluorine atoms provides an opportunity for low-background imaging by non-invasive techniques. Tumor bearing mice treated with fluorinated sialic acids will be imaged by 19F MRI. Since many tumor cells are hypersialylated, this technique may be useful for locating tumors before they are visible by other means. The Specific Aims for this study are to: (1) determine the scope of fluorinated sialic acid analogues tolerated for expression on cultured cells; (2) evaluate the static adhesion characteristics of cells expressing fluorinated sialic acids and study the mechanism of altered adhesion; (3) characterize the surfaces of cells expressing fluorinated carbohydrates; (4) evaluate the effect of cell-surface fluorination on tumor metastasis in mice; and (5) evaluate 19F MRI of tumor-containing mice expressing fluorinated carbohydrates. PUBLIC HEALTH RELEVANCE: The proposed study is relevant to cancer therapy and potentially to inflammatory disease because it explores a new strategy for reducing cell adhesion. The study is also relevant for cancer diagnosis because it may provide a way to image tumors by MRI.

描述（由申请人提供）：拟议的研究的目的是探索活细胞的生物学和生物物理特性，这些细胞在其表面上用不自然的氟化碳水化合物装饰。已经发现，这种细胞表面修饰可降低细胞粘附，因此可以提供一种治疗由细胞粘附（例如肿瘤转移和炎症）介导的人类疾病过程的方法。该项目的一部分旨在确定细胞表面氟修饰对与细胞粘附相关的生物学功能的影响。在鼠模型中，将通过生物发光成像来研究氟化的唾液酸降低肿瘤转移率或程度的能力。氟化分子在细胞表面的附着是通过与化学合成的氟化唾液酸类似物一起孵育并加工成氟化的糖蛋白和在细胞腺体上表达的糖脂的方法来完成的。该项目的一部分是确定在细胞表面表达氟化的唾液酸类似物的结构要求。同样，修饰分子在细胞表面的分布和性质将由二级离子质谱法，通过选择性切割的细胞表面分子的比色测定以及化学遗传学方法来确定。由于未修饰的细胞实际上没有氟化分子，因此氟原子的掺入为通过非侵入性技术进行低背景成像的机会。用氟化唾液酸处理的肿瘤轴承小鼠将通过19F MRI成像。由于许多肿瘤细胞被过度溶解，因此该技术对于通过其他方式可见之前定位肿瘤可能很有用。这项研究的具体目的是：（1）确定可耐受性盐酸类似物在培养细胞上的表达的范围； （2）评估表达氟化唾液酸的细胞的静态粘附特性，并研究改变粘附的机制； （3）表征表达氟化碳水化合物的细胞表面； （4）评估细胞表面氟化对小鼠肿瘤转移的影响； （5）评估表达氟化碳水化合物的含肿瘤的小鼠的19F MRI。公共卫生相关性：拟议的研究与癌症治疗有关，并且可能与炎症性疾病有关，因为它探索了一种新的降低细胞粘附的策略。该研究也与癌症诊断有关，因为它可能会提供MRI成像肿瘤的方法。