AlphaVbetaIII Activation in Blood and Endothelial Cells in Angiogenesis

血管生成过程中血液和内皮细胞中的 AlphaVbetaIII 激活

• 批准号: 8260296
• 负责人: Tatiana V Byzova
• 金额: $ 32.73万
• 依托单位: CLEVELAND CLINIC LERNER COM-CWRU
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-04-15 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8260296
• 关键词: Active Sites; Adhesions; Adult; Agonist; Biological Assay; Biology; Blood; Blood Cells; Blood Platelets; Blood Vessels; Blood capillaries; Bone Marrow; Bone Marrow Cells; Bone Marrow Transplantation; CXCR4 gene; Cell Adhesion; Cells; Cellular biology; Chimera organism; Complex; Endothelial Cells; Endothelium; Event; Growth; Imagery; Immune; In Vitro; Injection of therapeutic agent; Injury; Integrin beta3; Integrins; Ischemia; Knock-in Mouse; Knock-out; Knockout Mice; Malignant Neoplasms; Mediating; Modeling; Molecular; Mus; Organism; Pathologic Neovascularization; Pathology; Phosphorylation; Play; Process; Receptor Signaling; Recovery; Recruitment Activity; Regulation; Role; Stromal Cell-Derived Factor 1; Structure; Testing; Tissues; Transgenic Organisms; Tyrosine Phosphorylation; Vascular Endothelial Growth Factor Receptor-2; Vascular Endothelial Growth Factors; Virus; Wild Type Mouse; Wound Healing; angiogenesis; capillary; cell type; in vivo; in vivo Model; migration; mouse model; mutant; neovascularization; novel; novel therapeutics; operation; receptor; response; tumor; tumor growth; wound

The B3 subfamily of integrins are two-way signaling receptors that play essential roles in cell biology. Their influences on platelet function and vascular biology are particularly prominent. aVB3 receptor serves as a crucial regulation of angiogenesis, the process of blood vessel growth in adult organism which underlies a number of pathologies, including ischemic injury, cancer and tissue repair. Recent studies demonstrated that angiogenesis is a systemic process where vascular cells coordinate actions with immune cells of blood and tissue origin, and circulating blood components. Using a variety of in vivo models we have shown that activation of aVB3 occurs on endothelium at the sites of active angiogenesis and appears to control several angiogenesis-dependent responses including recovery after ischemia, tumor growth and wound healing. Using a knockin mouse model expressing mutant form of B3 unable to undergo phosphorylation, we demonstrated that B3 phosphorylation is essential for neovascularization in vivo. However, abnormal angiogenesis in B3 knockin mice was completely reversed by bone marrow transplantation was and appear to be dictated primarily by B3 integrin on bone marrow derived (BMDC) cells. Many of these recruited cells express CXCR4, a receptor for SDF-1. Moreover, SDF-1 treatment of BMDC seems to modulate cell adhesion via (33 integrin. These studies identified a novel and unconventional function of B3 integrin in angiogenesis and emphasizes that the process of angiogenesis involve co-operation of numerous cell types and tissues. The overall hypothesis to be tested is that aVB3 activation and phosphorylation are essential for in vivo cooperation between blood, bone marrow-derived and endothelial cells. The following Specific Aims are proposed to test our hypothesis: Aim I. To assess the role of p3 integrin activation and phosphorylation on the interactions between endothelial, bone marrow derived cells and platelets during angiogenesis in vivo. Double transgenic lines, DiYF-GFP and p3-/- GFP mice will be utilized for visualization of BMDC in bone marrow chimeras. We will also determine the role of platelet B3 on angiogenesis and recruitment of BMDC. Aim II. To assess the molecular and cellular mechanisms controlling interaction between circulating blood cells and endothelium and determine the role of p3 integrin in this process. Endothelial and BMDC cells from WT, B3-/- and B3 knockin mice as well as cells characterized by impaired integrin activation (from Project 1 and 2) will be used. Aim III. To assess the role of integrin activation in the process of p3 integrindependent adhesion of BMDC to endothelium. We will determine the role of SDF-1/CXCR4 axis in integrinmediated responses. These studies will delineate the cellular and molecular mechanisms of angiogenesis and result in identification of novel therapeutic strategies to treat ischemia, wound and other pathologies.

整合素亚家族B3是双向信号受体，在细胞生物学中发挥重要作用。它们对血小板功能和血管生物学的影响尤为突出。AVB3受体是血管生成的重要调节因子，是成年生物体血管生长的过程，是许多病理过程的基础，包括缺血损伤、癌症和组织修复。最近的研究表明，血管生成是一个全身性的过程，血管细胞与血液和组织来源的免疫细胞以及循环中的血液成分协调行动。利用各种体内模型，我们已经证明aVB3的激活发生在血管生成活跃的部位的内皮细胞上，并且似乎控制着一些血管生成依赖的反应，包括缺血后的恢复、肿瘤生长和伤口愈合。使用敲门小鼠模型 表达突变形式的B3不能发生磷酸化，我们证明了B3的磷酸化对体内新生血管是必不可少的。然而，骨髓移植完全逆转了B3敲门小鼠的异常血管生成，而且似乎主要是由骨髓来源的B3整合素(BMDC)决定的。许多这些被招募的细胞表达SDF-1的受体CXCR4。此外，SDF-1处理骨髓间充质干细胞似乎通过整合素(33整合素)调节细胞黏附。这些研究发现了B3整合素在血管生成中的一种新的和非常规的功能，并强调血管生成过程涉及多种细胞类型和组织的合作。需要检验的总体假设是aVB3激活和 磷酸化对于血液、骨髓源性细胞和内皮细胞之间的体内协作是必不可少的。 目的1.评估p3整合素活化和磷酸化在体内血管生成过程中对内皮细胞、骨髓源性细胞和血小板相互作用的影响。将利用两个转基因系DiYF-GFP和p3-/-GFP小鼠在骨髓嵌合体中显示BMDC。我们还将确定血小板B3在血管生成和BMDC募集中的作用。目的II.评价控制循环血细胞与内皮细胞相互作用的分子和细胞机制，并确定p3整合素在这一过程中的作用。将使用来自WT、B3-/-和B3敲击小鼠的内皮细胞和BMDC细胞，以及以整合素活性受损为特征的细胞(来自项目1和2)。目的III.评估整合素激活在p3整合素非依赖过程中的作用 骨髓间充质干细胞与内皮细胞的黏附。我们将确定SDF-1/CXCR4轴在整合素介导的反应中的作用。这些研究将描绘血管生成的细胞和分子机制，并确定治疗缺血、创伤和其他病理的新治疗策略。