Liver Regeneration as a Model for Angiogenesis

肝脏再生作为血管生成的模型

• 批准号: 7187422
• 负责人: DONNA BEER STOLZ
• 金额: $ 22.03万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-08-15 至 2009-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7187422
• 关键词: Abbreviations; Adult; Allogenic; Angioblast; Architecture; Area; Attention; Beer; Biochemical; Blood Vessels; Blood capillaries; Bone Marrow; Bromodeoxyuridine; Cell Death; Cell Line; Cell Proliferation; Cell physiology; Complex; Condition; Data; Embryo; Endothelial Cells; Engraftment; Evaluation; Event; Excision; Explosion; Extracellular Matrix; Female; Fluorescent in Situ Hybridization; Goals; Grant; Green Fluorescent Proteins; Growth; Growth Factor; Guns; Hand; Hepatic; Hepatocyte Growth Factor; Hindlimb; Homing; In Situ; Injury; Ischemia; Lead; Liver; Liver Circulation; Liver Regeneration; Modeling; Modification; Morphology; Neuropilin-1; Partial Hepatectomy; Physiologic Neovascularization; Physiological; Physiological reperfusion; Platelet-Derived Growth Factor; Process; Proliferating; Rattus; Reperfusion Injury; Reperfusion Therapy; Research Personnel; Resources; Role; Scanning Electron Microscopy; Seminal; Signal Transduction; Sinusoidal Infiltration; Site; Source; Stimulation of Cell Proliferation; Structure; Surface; System; Techniques; Time; Tissues; Transmission Electron Microscopy; Transplantation; Tumor-Associated Vasculature; Urokinase; Vascular Endothelial Growth Factors; Vascularization; Work; angiogenesis; base; capillary; cell growth; clinically relevant; comparative; day; erucylphosphocholine; functional restoration; injury and repair; liver cell proliferation; liver function; liver transplantation; male; migration; neovascularization; programs; receptor; repaired; response; response to injury; success; vasculogenesis

DESCRIPTION (provided by applicant): Angiogenesis is the process whereby new blood vessels sprout from existing vessels and requires that the specialized resident cells lining the vasculature, the endothelial cells (ECs), proliferate, migrate and differentiate spatially and temporally in response to specific signals. Vasculogenesis, on the other hand, has only recently emerged as an alternative mechanism of blood vessel growth in adult tissues and is the result of homing and engraftment of circulating EC precursors (ECPs) of bone marrow origin to areas of neovascularization. Both events are known to occur within the liver vasculature under very different conditions of growth, injury and repair, but the extent of each and the mechanisms by which they proceed in each case is completely unknown. The overall goal of this proposal is to determine the specific growth factor signaling events that induce angiogenic versus vasculogenic blood vessel growth in the context of liver and determine the subsequent microenvironmental milieu that induces EPC recruitment and/or differentiation of the liver-specific sinusoidal endothelial cell (SEC) fenestrated morphotype. Two paradigms of clinically-relevant liver repair allow us to spatially and temporally detail the growth factor signaling events and evaluate sinusoidal ultrastructure and liver-specific SEC function in the rat. AIM I: Growth factor and microenvironmental interactions will be examined at the sinusoidal surface following 70% partial hepatectomy (PHx) since there is initially extensive hepatocyte proliferation in the absence of EC proliferation until 96 hr post-PHx, resulting in avascular hepatic foci. Subsequent proliferation and infiltration of the SEC into these avascular parenchymal clusters and reestablishment of the normal hepatic architecture provides a well-timed model for evaluating physiological angiogenesis. AIM II: Angiogenic and vasculogenic events will be examined concurrently using an allogeneic liver transplant model (dual cross strain and female to male transplants, non-GFP to GFP rats) to ascertain the source of SEC (host vs. graft) and determine extent of recipient and donor involvement in SEC engraftment and/or proliferation. Prior to transplantation, livers are stored under cold, ischemic conditions for 18 h, and upon transplantation (warm reperfusion), a majority of the SEC slough off immediately from the sinusoidal surface. Remarkably, within 24 hr, the SEC lining has nearly completely repopulated at least partially from ECPs, but microvascular remodeling, morphological and functional modification occurs over subsequent days. Comparative analysis of these two systems will elucidate both similar and dissimilar growth factor signaling mechanisms and the role of the microenvironment that control these events and potentially lead to optimization of therapies that will reflect the specific requirements for injury based liver neovascularization.

描述（由申请人提供）：血管生成是新血管从现有血管中长出的过程，需要衬在血管系统中的特化驻留细胞（内皮细胞（EC））响应特定信号在空间和时间上增殖、迁移和分化。另一方面，血管发生只是最近才作为成人组织中血管生长的替代机制出现，并且是骨髓来源的循环EC前体（ECP）归巢和植入到新血管形成区域的结果。已知这两种事件在非常不同的生长、损伤和修复条件下发生在肝血管系统内，但每种情况下的程度和发生机制完全未知。本提案的总体目标是确定在肝脏背景下诱导血管生成与血管生成血管生长的特定生长因子信号传导事件，并确定诱导EPC募集和/或肝脏特异性窦状内皮细胞（SEC）有孔形态型分化的后续微环境环境。临床相关的肝修复的两个范例使我们能够在空间和时间上详细描述生长因子信号传导事件，并评估大鼠肝窦超微结构和肝脏特异性SEC功能。目标一：在70%部分肝切除术（PHx）后，将在肝窦表面检查生长因子和微环境相互作用，因为在PHx后96小时之前，在不存在EC增殖的情况下，最初存在广泛的肝细胞增殖，导致无血管肝灶。SEC随后增殖和浸润到这些无血管的实质簇中，并重建正常的肝脏结构，为评价生理性血管生成提供了一个适时的模型。AIM II：将使用同种异体肝移植模型（双交叉品系和雌性至雄性移植，非GFP至GFP大鼠）同时检查血管生成和血管生成事件，以确定SEC的来源（宿主vs.移植物），并确定受体和供体参与SEC植入和/或增殖的程度。在移植之前，将肝脏在冷的缺血条件下储存18小时，并且在移植（热再灌注）时，大部分SEC立即从正弦表面脱落。值得注意的是，在24小时内，SEC衬里几乎完全重新填充，至少部分来自ECP，但微血管重塑，形态和功能修饰发生在随后的几天。这两个系统的比较分析将阐明相似和不同的生长因子信号传导机制和控制这些事件的微环境的作用，并可能导致优化的治疗，这将反映基于损伤的肝脏新血管形成的具体要求。